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Online Events on Medical laboratories (past events)

Online Events on Medical laboratories are events that address medical laboratories new advancements, innovations, services, regulations and more. These gatherings serve as forums for collaboration, knowledge exchange, and strategy development, aiming to drive positive change and improve healthcare outcomes for diverse populations.....

Some of the topics covered in Online Events on Medical laboratories are clinical, laboratory medicine and medical laboratory.

Online Events on Medical laboratories bring together health professionals, researchers, policymakers, and stakeholders in the healthcare industry involved in medical laboratories topics.

Related topics
Showing 613 conferences
International Virtual Conference on Nursing Research, Patient Safety and Healthcare
Oct 2023
Evaluating Biopharma: Continuous Bioprocessing
Oct 2023
Sri Lanka Medical Association (SLMA) International Medical Congress
Jul 2023
Good Laboratory Practice & Good Clinical Laboratory Practice
May 2023
Comparability for Biologics
Apr 2023
Life Sciences, Clinical Trials, Patient Recruitment & Retention
Jan 2023
Evaluating Biopharma - Cell Therapy Strategies
Dec 2022
HPAPI Handling & Manufacturing Summit
Sep 2022
Clinical Project Management MasterClass
Sep 2022
International Conference on Healthcare Engineering (ICHE)
Sep 2022
International Conference on Nursing Education, Patient Safety and Healthcare
Jul 2022
Analytical Instrument Qualification & Validation - Use of Excel and FDA Audit Preparation
Jul 2022
How to Apply for a Breakthrough Therapy Designation and Win It
Jun 2022
International Congress of Micro-Immunotherapy (ICoMI)
Jun 2022
Medical Device Regulations & Compliance Summit
May 2022
Pharmacokinetics (PK) / Pharmacodynamics (PD) Studies in Drug Discovery and Development
May 2022
Packaging and Labeling in Pharmaceutical Product Development - Best Practices
May 2022
Scholars International Webinar on Advances in Drug Discovery and Development
Mar 2022
Contemporary Challenges in Bioethics and Clinical Research : AI, Big Data, and Privacy
Mar 2022
International Conference on Clinical Research and Clinical Trials
Mar 2022
3-Hour Virtual Seminar on IQ, OQ, PQ in the Verification and Validation Process
Mar 2022
Quality Control Laboratory Compliance - cGMPs and GLPs
Feb 2022
Regulated LC-MS Bioanalysis Masterclass
Jan 2022
UCG on Diabetes and Endocrinology Conference
Jan 2022
Cleaning Validation for Pharma
Dec 2021
Early & Managed Access Programmes
Nov 2021
Vendor/CRO Management and Oversight MasterClass
Nov 2021
Webinar: Harnessing the Power of Bispecific Antibodies
Oct 2021
Investigator Initiated Trials
Sep 2021
Healthcare Planning & Infrastructure Expo (HPIE)
Sep 2021
Patient Recruitment, Engagement and Support Summit
Aug 2021
Bangladesh Medical & Healthcare Virtual Expo
Jun 2021
Risk-Based Validation of Laboratory Computerised Systems MasterClass
May 2021
ProcureCon Pharma
May 2021
Conference on Laboratory Medicine & Pathology
Apr 2021
Clinical Trials V-Forum
Apr 2021
Global Experts Meeting on Pathology and Laboratory Medicine
Apr 2021
Virtual On-line Conference on Clinical Trials & Clinical Research
Mar 2021
Risk Management in Medical Devices Industry
Mar 2021
International Conference on Clinical Trials
Feb 2021
Molecular Med TRI-CON
Feb 2021
International Conference on Clinical Chemistry and Laboratory Medicine
Feb 2021
Data Integrity: FDA/EU Requirements and Implementation
Jan 2021
Clinical Trial Innovation Summit
Nov 2020
Laboratory Inspection and Auditing
Oct 2020
FDA`s Regulation of Regenerative Medicine including Stem Cell Treatments and Tissue Engineering Training
Oct 2020
Digitalpathology
Oct 2020
Digital Clinical Biomarkers and World CDx Summit
Oct 2020
Risk Management in Clinical Research
Sep 2020
International Conference on Pharmacoepidemiology and Clinical Research
Sep 2020
Validation, Verification and Transfer of Analytical Methods (Understanding and implementing guidelines from FDA/EMA, USP and ICH)
Jul 2020
Issues in Calibrations and Accuracy in Method Validation
Jun 2020
Predictive Analytics World Healthcare
May 2020
Confidentiality of Substance Use Disorder Patient Records; Complying with the New Federal Law 42 CFR Part 2
Nov 2019
Effective Supplier Management Programs
Aug 2019
Biosafety and Blood borne Pathogen Safety in the Lab
Jul 2019
6-Hour Virtual Seminar on Adaptive Design for Clinical Trials
Jul 2019
Auditing Laboratory Data Systems
Jul 2019
Basics of Testing Associated with Sterilization Validation and Routine Processing
Jul 2019
Establishing Appropriate Quality Metrics and Key Performance Indicators (KPIs)
Jul 2019
CAPA, Failure Investigation and Root Cause Analysis to Meet FDA Expectations
Jun 2019
Demystifying the Canadian Drug and Health Products Regulatory Landscape
Jun 2019
Auditing Laboratories Conducting Assays Supporting Biologics
Jun 2019
Power Analysis for Sample Size Calculations
Jun 2019
Onboarding: From Entry-Level to Senior Executive
Jun 2019
Solving Statistical Mysteries – What does the FDA want
Jun 2019
How to Prepare Yourself for FDA`s on-going Part 11 Inspection Program
Jun 2019
CAPA Simplified - A one-form, easy-to-complete, method for simplifying your CAPA Process
Jun 2019
Project Management for Non-Project Managers
Jun 2019
Implementing a Compliant Stability Program for Biologics
Jun 2019
3-Hour Virtual Seminar on Qualification (IQ, OQ, PQ) and Validation of Laboratory Equipment and Systems for Regulated Industries
May 2019
New Elemental Impurities Tests for Pharmaceutical Products According to the New ICH Q3D and USP 232/233 Guidelines
May 2019
Documentation of Medical Necessity - Focus for OIG and other auditors
May 2019
Validation and Use of Excel Spreadsheets in FDA Regulated Environments
May 2019
Stability Studies & Estimating Shelf Life
May 2019
Quality Control for Microbiological Media and Reagents
May 2019
Compliance Measures for Case Managers
May 2019
GMP Environmental Monitoring in Pharmaceutical Clean Rooms
May 2019
Ensuring your Site is Ready for an FDA Inspection
Apr 2019
Risk Management in Clinical Research
Apr 2019
3-Hour Virtual Seminar on Safety Audits and Pharmacovigilance (PV) Inspections
Apr 2019
Analytical Method Validation and Transfer
Apr 2019
Compliance with the New ICH GCP Revision 2 Addendum
Apr 2019
QbD Approach to Analytical Method Lifecycle: Design, Development, Validation and Transfer
Mar 2019
FDA Inspections - Do`s and Don`ts
Mar 2019
Theory and Practice of Near-Infrared Spectroscopy
Mar 2019
FDA`s Quality Metrics - Latest Advances
Mar 2019
Sterilization Processes - The Methods, Parameters and Deficiencies
Mar 2019
Water System Biofilm Control and Microbial Monitoring Myths
Mar 2019
Is it Method Verification or Validation, or Just Semantics
Feb 2019
Analytical Method Transfer According to USP General Chapter-1224
Feb 2019
Measurement Systems Analysis
Feb 2019
Validation and Use of Excel Spreadsheets in FDA Regulated Environments
Feb 2019
Tips and Techniques for Handling Missing Data (Statistical Techniques)
Jan 2019
Data Governance for Computer Systems Regulated by FDA
Jan 2019
Design History Files (DHF), Device Master Records (DMR), Device History Records (DHR), Technical Files , Design Dossiers - The Requirements
Jan 2019
Sample Size Determination for Design Validation Activities
Dec 2018
Handling Situations Where Regulation E and ACH Don`t Align
Dec 2018
Medical Devices - ISO 13485
Dec 2018
FDA Regulations for Analytical Instrument Qualification and Validation – Comprehensive Best Practices
Dec 2018
Seasonal Influenza Vaccines- Current Concepts and Future Trends for Effective Immunization
Dec 2018
Quality Control for Analytical Materials used in Microbiology Laboratories
Dec 2018
Excel Formulas and Functions
Nov 2018
Control-Analysis Instrumentation used in PAT Continuous Manufacturing
Nov 2018
Auditing for Microbiological Aspects in Pharmaceutical Manufacturing
Nov 2018
Process Verification and Validation
Nov 2018
How to Write SOPs which are Compliant for Inspections for a GXP Compliance
Nov 2018
Good Documentation and Record Keeping Best Practices (FDA & EMA)
Nov 2018
Ensuring Integrity and Security of Laboratory Data
Nov 2018
Requirements for IQ, OQ and PQ Quality Protocols
Oct 2018
Sterilization of Pharmaceutical Products and Medical Devices
Oct 2018
Aseptic Process Overview and Validation
Oct 2018
Troubleshooting Ethylene Oxide (EO) Processes
Oct 2018
Powerful Closed-loop CAPA - Meeting FDA Expectations
Oct 2018
FDA`s New Enforcement of 21 CFR Part 11
Sep 2018
Changes under the HIPAA Omnibus Rule - What`s New
Sep 2018
cGMPs in the Quality Control Laboratory
Sep 2018
Quality Agreements Made Easy
Sep 2018
How FDA Trains its Investigators to Review CAPA and What You Should Do to Prepare
Sep 2018
Compliance for Risk Based Approaches for Clinical Trials
Sep 2018
CGMP controlled Raw Materials
Sep 2018
Onboarding Employees in a GMP Environment: Best Practices for Foundational Employee Success
Sep 2018
CMS Hospital CoP and TJC Telemedicine Standards, Telemedicine Credentialing and Privileging
Jul 2018
New Revision of USP <1058>: Analytical Instrument Qualification
Jul 2018
Laboratory Investigations for Out of Specification Results
Jul 2018
Opioid Abuse in the Workplace: Using Effective Drug Testing and Policies to Reduce the Pain of the Painkiller Epidemic
Jul 2018
Sunshine Act Reporting: Clarification for Clinical Research
Jul 2018
Good Documentation Guideline (Chapter <1029> USP)
Jul 2018
Root Cause Analysis (RCA) in the Laboratory - Addressing Non-Conformances
Jul 2018
Forced Degradation Studies/ Biologics Stability Programs for Biopharmaceuticals
Jul 2018
How to Make Sure Your Foreign Vendors are FDA Compliant and Stay that Way
Jul 2018
Deviation Investigation Best Practices: Ensuring Correct Content and Conclusions
Jul 2018
Patients Suing Under HIPAA
Jul 2018
Develop a Compliant Validation Protocol and Analytical Procedures according to the FDA Guidance and USP Good Documentation Practices
Jul 2018
Ligature Risks: Ensuring Compliance with the CMS Hospital CoPs and TJC Requirements
Jun 2018
510(k) Documentation Best Practices for Software or Software Enabled Medical Devices
Jun 2018
Water System Investigation `How-To`s` and Example Case Studies
Jun 2018
Biocompatibility Testing; what you need to know
Jun 2018
Food Fraud in the Organic Industry
Jun 2018
Oversight of CROs-Vendors-CMOs
Jun 2018
Off label Promotion of Drugs and Medical Devices - FDA`s Latest
Jun 2018
Does your QC lab do GMP and non-GMP activities?
May 2018
Why and How - Verification of Compendial Methods - USP [1226]
May 2018
Investigator Reporting Responsibilities: AEs, Unanticipated Problems, Modifications, and Deviations
May 2018
Document Control and Change Control Process in GxP/GMP Environment
May 2018
GMP Expectations for Products Used in Early Phase IND Studies
May 2018
Health Product Marketing authorization in Brazil - Documentation, Approval Process, Labeling, Advertising and Post Market Vigilance
May 2018
Fundamentals of Risk Management in Clinical Research
May 2018
Auditing Analytical Laboratories for FDA Compliance
May 2018
How to Comply with 21 CFR 11 Requirements for Electronic Medical Records
May 2018
Failure Modes and Effects Analysis
Apr 2018
Drug Master Files: Understanding and Meeting your Regulatory and Processing Responsibilities
Apr 2018
Differences Between ISO 13485 & ISO 9001 - and How to Choose Which One to Implement
Apr 2018
FDA Clinical Trial Auditing and the due diligence Companies should conduct as part of their monitoring program
Mar 2018
Ensuring Data Integrity in Method Validations
Feb 2018
Trial Master File for Clinical Data Systems Regulated by FDA
Jan 2018
The Value of a Human Factors Program
Jan 2018
21 CFR Part 11 Compliance - Ensuring Data Integrity and Safety in Clinical Research
Jan 2018
Why are we Seeing More Independent Data Safety Monitoring
Dec 2017
Analytical Method Validation Under Good Laboratory Practices - GLPs
Dec 2017
Dealing with Performance Issues
Nov 2017
FDA`s Latest Regulations for Tobacco Industry Effective 8-2016
Nov 2017
AAMI TIR 45: Agile Meets Software Standards, and we all Win
Nov 2017
Medical Device Hazard Analysis Following ISO 14971
Nov 2017
The Future of Supply Chain - 7 Megatrends that will Transform the Global Marketplace
Nov 2017
Virtual Seminar on Analytical Method Validation Process
Nov 2017
World Clinical Medicine & Collaboration Forums
Oct 2017
Laboratory Instrument Qualification
Oct 2017
Managing Your FDA '483' Inspectional Observations
Oct 2017
FDA Regulations for Analytical Instrument Qualification and Validation Processes
Oct 2017
21 CFR Part 11 Compliance for Computer Systems Regulated by FDA
Oct 2017
Laboratory Instrument Calibration
Oct 2017
GLP Quality System Essences and Comparison with GMP
Oct 2017
Effective Training Practices for FDA Compliance
Sep 2017
Document Control and Training
Sep 2017
Best Practices for an Effective Cleaning Validation Procedures
Sep 2017
Investigation of Out-Of-Specification Laboratory Results
Sep 2017
2018 ICD-10-CM Update for Cardiology
Sep 2017
New Relationship between the Data Controller, Data Processor and the Data Subject
Sep 2017
FDA Regulations for Environmental Monitoring (EM) Program
Aug 2017
Laboratory-Developed Tests: Why does FDA think they can Regulate them, and why do others think they Cannot
Aug 2017
How to Prepare for and Host a FDA Inspection and Respond to 483`s
Aug 2017
Building a Validation Program From Top to Bottom
Aug 2017
Understanding Aseptic Technique and Cleanroom Behavior
Jul 2017
Laboratory Accreditation: Getting there is just the beginning
Jul 2017
Personnel Training to Assure FDA and ISO Compliance
Jul 2017
How To Establish an Effective Chief Compliance Officer`s (CCO) or Chief Risk Officer`s (CRO) Function - Organization and Responsibilities
Jun 2017
Complaints, Servicing and FDA Reporting
Jun 2017
Improving Process Stability and Capability - Tips, Traps and Guidance
Jun 2017
Compliance with ICH GCP R2 Addendum for Auditors
Jun 2017
Steam Sterilization Microbiology and Autoclave Performance
Jun 2017
FDA Policy and Goals Regarding the 483 Response
Jun 2017
FDA`s Expedited Development and Approval Programs: Taking the Mystery out of Expedited Approvals
May 2017
Elements of a Corrective and Preventive Action (CAPA) Program and Uses of CAPA Data
May 2017
New FDA or EMA and USP Guidelines for Transfer of Analytical Methods
May 2017
Phase I GMPs
May 2017
Best Practices for Preparation for, Behavior during, and Response to an FDA Inspection
Apr 2017
Medical Records: Responding to Subpoenas and Investigations
Apr 2017
PMBA - Project Management Business Administration
Apr 2017
Medical Necessity: Can you define it, Capture it, Document it
Apr 2017
Classifying Medical Devices - US and EU
Mar 2017
Powers of Attorney: Medical Records Release Concerns
Feb 2017
Trial Master File (TMF): FDA Expectations from Sponsors and Sites
Feb 2017
Capturing Justifications in Change Control, Risk Assessment, Validations, and Investigations
Feb 2017
Microsoft Excel Series - Part 3: Beyond IF and Excel Macros
Feb 2017
Clinical Trial Monitoring: A Sponsor Responsibility
Feb 2017
Laboratory Inspection Readiness - Implementing GMPS for the Pharmaceutical Laboratory
Feb 2017
Essentials of Complaint Handling and Medical Device Reporting
Feb 2017
Latin America Regulatory Compliance: Current Challenges in Argentina, Brazil and Mexico
Feb 2017
Best Practices for Project Management of Clinical Trials
Feb 2017
The Sunshine Act: Reporting for Clinical Trials
Jan 2017
The Investigational Medicinal Product Dossier (IMPD): EU CTA vs. FDA IND: Comparing the Content and Agency Expectations
Jan 2017
How to Write HIPAA Policies and Procedures
Jan 2017
Conducting Effective Investigations of Out of Specification and Atypical Laboratory Results
Jan 2017
Recalls, Removals, and Market Corrections in Compliance with FDA and ISO Requirements
Jan 2017
Navigating the New European Clinical Trial Regulation (EUCT Regulation 536-2014)
Jan 2017
Transfer of Analytical Methods and Procedures: FDA Requirements and Strategies and Tools for Implementation
Dec 2016
Innate Immunity: The line of defence
Nov 2016
Determining Sample Size: How to Ensure You Get the Correct
Nov 2016
Sanitizers for the Food Industry
Nov 2016
Good Laboratory Practice Regulations - Introduction and Strategies for Implementation
Nov 2016
Good Laboratory Practices (GLPs) - Comparing and Contrasting with Good Manufacturing Practices (GMPs)
Nov 2016
Laboratory Instrument Calibration: Current FDA Regulatory Requirements and Best Practices
Oct 2016
Laboratory Investigation Out-of-Specification Results
Oct 2016
Design and Execution of Stability Studies for Biologics
Oct 2016
Auditing Clinical Trials for Good Clinical Practice (GCP) Compliance
Oct 2016
Calibration in the Laboratory
Oct 2016
Production and Process Control: Building a Robust System for Medical Device Companies
Oct 2016
HIPAA Training for the Compliance Officer
Oct 2016
GCP: The IND, How to Gain Approval for Clinical Trials in the USA
Sep 2016
Sub-visible Particulates in Biological products
Sep 2016
Legal, Regulatory and Policy Issues Related to Computer System Validation as the FDA Regulates Tobacco Products
Sep 2016
Defining and Managing Protocol Deviation/Violation/Exception
Sep 2016
Business Continuity or Disaster Recovery Planning
Aug 2016
Meeting the Toughest Laboratory Accreditation Requirements (Part-2)
Aug 2016
Clinical Trials be at Risk for Potential Fraudulent Billing. Conducting a Billing Risk Assessment and Coverage Analysis are Essential for Proper Billing.
Aug 2016
Changes to the Common Rule (45 CFR 46) : What this means for you
Aug 2016
Lyophilization: What you Need to Know, Validation and Regulatory Approaches
Aug 2016
Chiropractic & ICD-10
Aug 2016
How to do a Risk Analysis
Aug 2016
Laboratory Safety - Covering Issues such as Compressed Gases, Cryogenic Materials and Glassware, etc.
Aug 2016
What Sample Size Do I Need
Aug 2016
How to Prepare for Increased HIPAA Enforcement
Aug 2016
New CMS CoP Regulations for Managing Grievances and Complaints: What Hospitals Should Know about the CMS and Joint Commission and DNV Standards
Aug 2016
Writing Effective SOPs for the GMP Laboratory
Jul 2016
Creating an Effective Lab Safety Program
Jul 2016
Laboratory Management with ISO/IEC 17025:2-Part Series
Jul 2016
Understanding and Implementing an Effective Laboratory Quality Management System to comply with ISO/IEC 17025
Jul 2016
USP <71> Sterility Testing: New Harmonization with International Compendia and Overview
Jul 2016
Electronic Data Integrity in a GxP Environment: Managing the Data Lifecycle for Compliance
Jun 2016
Analytical Method Validation under Good Laboratory Practices (GLPs)
Jun 2016
Transfer of Analytical Procedures According to the New USP Chapter [1224]
Jun 2016
Investigating and Reporting Adverse Reactions Related to Human Cells, Tissues, and Cellular and Tissue Based Products (HCT/Ps)
Jun 2016
Adverse Event Reporting: Site and Sponsor Reporting Requirements for Investigational Products
May 2016
Lifecycle Approach to Analytical Methods: Incorporating QbD Principles into Method Development, Validation and Transfe
May 2016
Validation of a HPLC/UPLC Methodology
May 2016
Evaluating the Effectiveness of a Corporate Compliance Program
Mar 2016
Mathematics of Terminal Sterilization - Probability of Survival Approach -vs- Overkill Approach
Mar 2016
Antimicrobial effectiveness test USP [51] : Overview and New Content Proposals
Mar 2016
21 CFR Part 11 (Electronic Records/Signatures) Compliance for Computer Systems Regulated by FDA
Feb 2016
Investigational Device Accountability
Jan 2016
Cleanroom Monitoring & Maintaining a Quality Environment : Overcoming USP [797] Common Non-Compliance Issues
Jan 2016
Avoiding 12 Most Common Statistical Errors in Clinical Research
Jan 2016
FDA`s New Enforcement of 21 CFR Part 11
Jan 2016
From the ER to the OR - IQCP Compliance for CAP Accredited Hospitals
Jan 2016
Registration & Listing, FDA Inspection Strategies and Compliance Initiatives - Medical Device
Dec 2015
Objectionable Microorganisms: Considering the Risk
Dec 2015
Development regulatory affairs for Oncology Medicinal Products
Oct 2015
TM`s world drug discovery online conference
Oct 2015
A look at 510(k) changes
Oct 2015
Risk Management in Clinical Trials
Oct 2015
Establishing an FDA-Compliant UDI System
Oct 2015
Orphan Medicinal Product Designation in the EU
Sep 2015
Calibration and Qualification in Analytical Laboratories
Sep 2015
Budgeting for Clinical Trials: Understanding Costs of a Study and Which Costs Sponsors are Responsible to Cover
Sep 2015
Creating Design History Files (DHF), the Device Master Records (DMR) and the Device History Records (DHR), Utilizing the Principles of Lean Documents and Lean Configuration
Sep 2015
Auditing QC and Contract Laboratories for GMP Compliance
Sep 2015
FDA`s enforcement of 21 CFR part 11 compliance
Sep 2015
Basic Requirements for Developing IQ and OQ Protocols
Sep 2015
Bullet Proof 510(k) - Latest FDA Proposed Changes to the Process
Sep 2015
Getting to Know FDA Audit Practices and the 10 Most Common Cited GMP Deficiencies
Aug 2015
Corrective Actions - Current Expectation of ISO 13485 and FDA Auditors
Aug 2015
PREPARING FOR IMMINENT FEDERAL HIPAA AUDITS (LEVEL:ADVANCE)
Aug 2015
Preparing for Imminent Federal Hipaa Audits (level:intermediate)
Aug 2015
How To Conduct Medical Device Risk Analysis Effectively (level: Advance)
Aug 2015
Failure Mode and Effects Analysis for Design Improvement and Design Control
Aug 2015
European Filing and Registration Procedures
Jul 2015
USP Hot Topics: What`s Hot Now and How to Track Coming Changes and Influence USP
Jul 2015
Supply-Chain Finance
Jul 2015
International Regulatory Cooperation Among Agencies
Jul 2015
Uncertainty of Measurement as Required by ISO/IEC Standard 17025:2005 for Lab Accreditation:An Environmental Microbiologist’s Perspective
Jul 2015
Development Regulatory Affairs for Oncology Medicinal Products
Jun 2015
Premarket Approval (PMA) agreement with FDA for the Medical Device Companies
Jun 2015
South East Asia Regulatory Compliance for Life Science Products, Live Webinar
Jun 2015
Writing Evaluation Reports-How to Write Evaluation Report
Jun 2015
U.S. FDA`s New Strategic Priorities 2014 - 1018 ()
Jun 2015
Conducting Observational Studies in US, Canada and Europe
Jun 2015
Monitoring Plans: 10 Rules of Effective Writing of Monitoring Plans
May 2015
The FDA Inspection: Preparation, Management, and Follow-Up
May 2015
Developing and Using the Product Risk Management File/Report
May 2015
Practical Application of HIPAA Risk Analysis
May 2015
Regulatory Aspects of Advanced Therapy Medicinal Products in the EU
May 2015
DHF, DMR, DHR, Technical File and Design Dossier - Key Requirements and Future Directions
May 2015
South East Asia Regulatory Compliance for Life Science Products - Hong Kong, Taiwan, Thailand, Singapore, Malaysia and Vietnam
Apr 2015
Is it Method Verification or Validation, or Just Semantics?
Apr 2015
cGMPs in the Quality Control Laboratory
Apr 2015
Quality System Regulations for Devicemakers: A Regulatory Approach
Apr 2015
Medical Packaging Validation Strategies, Planning for Success
Apr 2015
The Need and Role of Standard Operating Procedures in the Pharmaceutical and Medical Device Industries
Apr 2015
Issues with Risk Assessments for Cross Contamination of OSD Facilities
Apr 2015
China: Compliance Processes for Life Science Products (Company Establishment, Clinical Trials, Registrations, Renewals and Supply Chain Considerations)
Apr 2015
Designing Effective and Efficient Extractables or Leachables Studies for Biologics
Mar 2015
Biological Facility Design for Compliance
Mar 2015
Better Alternatives to Sampling Plans
Mar 2015
Institutional Review Boards (IRBs): The Changing Landscape and the Effect on the Conduct of Clinical Research
Mar 2015
Complaint Handling and Management: From Receipt to Trending
Feb 2015
Regulatory Perspectives of Clinical Project Management: Meeting FDA Requirements for Clinical Trials
Feb 2015
Clinical Trial Liability Lawsuits
Feb 2015
Blinding of Investigational Materials
Feb 2015
Deviations: What are they? Do you need to report?
Jan 2015
Personal Medicine and the Future of Health Care
Jan 2015
Benchmark for Cleaning Validation
Jan 2015
New Requirements for Sponsors and Laboratories for Analyzing Clinical Trial Samples to Meet GCP/GCLP Internationally
Jan 2015
EU Clinical Trial Regulation: New Requirements
Jan 2015
FDA Decisions For IDE Clinical Investigations
Dec 2014
Cosmetics and the Science of Beautiful Skin
Dec 2014
Clinical Trial Recruitment Methods and Metrics
Dec 2014
What are Serious Adverse Events & How do I Handle SAEs?
Nov 2014
Legacy System Replacement in an FDA-Regulated Environment
Oct 2014
Implementing the Best Practices for FDA Inspection Preparation and Management
Oct 2014
Pursuance of FDA draft guidance on analytical method validation for Drugs and Biologics
Sep 2014
Auditing, Qualifying and Controlling, Suppliers and Contractors for Pharmaceuticals and Medical Devices (Purchasing Controls)
Jul 2014
Integrating Risk Management into the CAPA System
Jul 2014
FDA Guidance Design Considerations for Pivotal Clinical Investigations for Medical Devices
Jul 2014
Best Practices With Submissions Under Medical Device User Fee Act (MDUFA)
Jun 2014
Best Practices for Documenting a Computer System Validation Process
Jun 2014
CAPA Training and Causes of Warning Letters due to Lack of Comprehension
Jun 2014
China: Compliance Processes for Life Science Products (Company Establishment, Clinical Trials, Registrations, Renewals and Supply Chain Considerations)
May 2014
GMP Compliance Audit: How Best to Prepare for It
Apr 2014
Good Documentation Practices for Clinical Trials
Feb 2014
Remediating Pharmaceutical Water System Biofilm - What to Do After It Gets Ahead of You
Nov 2013
FDA vs. EU Inspections - How to Prepare and What are the Differences
Nov 2013
Robust Corrective And Preventive Action (CAPA)
Nov 2013
510(k) for IVDs
Nov 2013
Unique Device Identification (UDI) Final Rules Overview
Nov 2013
CLIA (Clinical Laboratory Improvement Amendments) Guidelines on Quality Control and Quality Assessment
Oct 2013
Charging for Investigational Drugs: Current Application of 21 CFR Part 312 and the Expanded Access Rules
Oct 2013
Falsifying Data in clinical trials. What to report?
Oct 2013
Verification of Compendial Methods According to the Revised USP Chapter <1226>
Oct 2013
Understanding Disinfectant Qualification Studies – How to Avoid Errors
Sep 2013
Developing and Updating a ``Compliant`` Lab Compliance Plan (Medicare and Medicaid Focus)
Aug 2013
Oncology Trials Outsourcing
Jul 2013
Optimal capacity planning and resource allocation for a portfolio of clinical trials
Jun 2013
Introduction to Bioequivalence and Therapeutic Equivalence
Jun 2013
Shared facilities and the move to science based risk assessments
Jun 2013
Serious Product Quality Problems – Dealing with the Press and the Public
Jun 2013
The US FDA Quality System Regulation (QSR) – What Every Exective and Senior Manager Must Know
May 2013
FDA-Compliant Medical Device Reporting (MDR)
Apr 2013
Interactive Response Technologies for Clinical Trials
Apr 2013
Bridging the Gap: Co-Development of Targeted Therapeutics and Companion diagnostics in the US and EU
Apr 2013
China: Compliance Processes for Life Science Products: Company Establishment, Clinical Trials, Registrations - Webinar By GlobalCompliancePanel
Apr 2013
Best Practices for Preparation for, Behavior during, and Response to an FDA Inspection
Apr 2013
Best Practices for Conducting OOS Investigations (in Pharmaceutical Laboratories)
Apr 2013
How to Withstand an FDA Audit of your Facility
Apr 2013
Auditing the QC Microbiology Laboratory for FDA Compliance
Apr 2013
Key Factors to develop an effective CAPA system
Apr 2013
3-hr Virtual Seminar: Annual ICH GCP Refresher Course
Apr 2013
Designing a Clinical Protocol for Vaccine Clinical Trial
Apr 2013
Bioanalytical Methods Validation
Mar 2013
Quality Practices for Research and Development (R&D) CMC Laboratories
Mar 2013
Writing Clinical Data Queries - Best Practices and Pitfalls
Mar 2013
Risk Assessment - Compliance Using Easy To Fill Out Documentation
Mar 2013
Curtailing Microbial Excursions and Investigations in Pharmaceutical Water Systems
Mar 2013
You have a Sterility Failure or Bioburden Excursion - Now What?
Mar 2013
Why are we seeing more Independent Data Safety Monitoring (DMC) use in Clinical Research
Mar 2013
Maximizing the Performance & ROI in Clinical trials: A Personalized Approach
Feb 2013
Clinical Laboratory Incident Management Plan - GLP and FDA Compliance
Feb 2013
Advanced Cell Culture & Fermentation - Process Development & Manufacture
Feb 2013
The Clinical Trial Study Protocol (Advanced)
Feb 2013
Environmental Monitoring and Contamination Control Plan
Feb 2013
Making All Data Count: FDA Acceptance of non-US Clinical Trials
Feb 2013
Investigator Initiated Trials - What Are We Doing to Ensure Human Subject Protection?
Feb 2013
Training on Current ICH GCP Guidelines
Feb 2013
GMP Analytical Laboratory Audits - Planning, Preparation, Execution, and Resolution
Feb 2013
Deviation Management System
Jan 2013
Basic Cell Culture & Fermentation - Process Development & Manufacture
Jan 2013
Objectionable Microorganisms in Medicinal Products - Aseptic Environment
Jan 2013
Optimal Clinical Supply Planning for Global Drug Development
Jan 2013
Patient Reported Outcomes (PROs): Overview and Guidance for clinical trials and medical product labeling
Dec 2012
Quality Assurance at the (Clinical Research) Site: How to Develop a Manageable Plan
Dec 2012
Supplier Evaluation and Assessment: How to Meet FDA QSR and ISO 13485 Requirements in a Cost-Effective Manner -Webinar By GlobalCompliancePanel
Dec 2012
Managing Your Medical Device Reporting (MDR)Program for Compliance Success
Nov 2012
Auditing Analytical Laboratories for FDA Compliance
Nov 2012
Product Hazard Analysis and Risk Management Under ISO 14971 and FDA, ICH Q9
Nov 2012
Practical strategies to Improve Productivity in the Pharmaceutical Laboratory
Nov 2012
FDA Guidance Regarding Clinical Trials for Foods, Food Ingredients, and Dietary Supplements
Nov 2012
Process Validation for Medical Devices
Nov 2012
Design Control for Medical Devices
Nov 2012
Aspects to Consider for Clean Room Qualification and Operation
Nov 2012
Computer Systems Used in Clinical Trials
Oct 2012
Laboratory Water Systems: Necessary Water Specifications and Validation Challenges
Oct 2012
Avoiding 483 Observations and Warning Letters
Oct 2012
21 CFR Part 11: Ins and Outs of Audit Trails
Oct 2012
Live webinar on Preclinical studies regulatory requirements and principle of Good Laboratory Practices (GLP)
Oct 2012
System Based Inspections - Laboratory Controls
Oct 2012
21 CFR Part 11 and Annex 11; What you Need to Know to Pass the New Regulatory Audits
Oct 2012
Clinical Trials Drug Supply: Imports and Release Procedures for Shipping to Trial Sites
Oct 2012
CDISC – Insight, Impact and Implementation
Sep 2012
Clinical Trial Billing - Building a Compliant Process that Works!
Sep 2012
Successful 510(k) submission: Contents and Format
Sep 2012
Update on Unique Device Identifier for Device Manufacturers
Sep 2012
FMEA and Risk Management for Medical Devices
Sep 2012
21 CFR Part 11: How to Successfully Prepare for and Host an FDA Inspection
Sep 2012
Risk Assessment-Compliance Using Easy To Fill Out Documentation
Sep 2012
How to Select Best Practices a CRO ?
Sep 2012
Investigator Initiated (Sponsored) Trials – ISSs
Sep 2012
Incorporating Six Sigma DMAIC into CAPA
Sep 2012
Stability Studies for Vaccine Products
Sep 2012
Key Concepts in Successful Water System Sanitization - Webinar By GlobalCompliancePanel
Aug 2012
Validation and Use of Excel Spreadsheets in Regulated Environments - Webinar By GlobalCompliancePanel
Aug 2012
Addressing Impurities in Pharmaceutical Products: Impurities, Degradants, Residual Solvents and Elemental Impurities
Aug 2012
Human Behavior in Cleanrooms and Controlled Environments - Webinar By GlobalCompliancePanel
Aug 2012
Process Verification and Validation Planning and Execution
Aug 2012
Bullet Proof 510(k) - Latest FDA Proposed Changes to the Process - Webinar By GlobalCompliancePanel
Aug 2012
CE Marking for Medical Devices Including In Vitro Diagnostic Devices - Webinar By GlobalCompliancePanel
Aug 2012
Sterilization as a Benchmark for Cleaning Validation and Control - Webinar By GlobalCompliancePanel
Aug 2012
Common Sense Water System Validation - Webinar By GlobalCompliancePanel
Aug 2012
The Use and Mis-use of FMEA in Medical Device Risk Management
Jul 2012
New QC Based on Risk Management: A Collaboration between CLIA and CLSI
Jul 2012
Complaint Handling and Management: From Receipt to Trending - Webinar By GlobalCompliancePanel
Jul 2012
Ethics and Scientific Misconduct in Regulated Studies
Jul 2012
Software validation and 21 CFR Part 11 remediation planning: FDA inspection strategies
Jul 2012
Specialized Formulations – Biomolecules
Jul 2012
HPLC Outside the Box: How to Think Like a Chromatographer
Jul 2012
HPLC Outside the Box: Beating Your Competitors to Market
Jul 2012
Navigating the Japan Regulatory and Clinical Trial Environment; Conducting Clinical Studies in Japan
Jul 2012
Clinical Trial Auditing - Identifying risks and building a more compliant and successful trial
Jul 2012
The U.S. FDA`s Tougher Supplier Controls - Webinar By GlobalCompliancePanel
Jul 2012
Good Pharmacovigilance Practice - Inspection and Audits - Webinar By GlobalCompliancePanel
Jul 2012
Understanding and Implementing ISO 17025
Jun 2012
Prepare for Tougher cGMP Compliance Audits - Webinar By GlobalCompliancePanel
Jun 2012
Understanding Costs of a Study for Clinical Trials - Webinar By ComplianceOnline
Jun 2012
REMS Update: Risk Evaluation and Mitigation Strategies - Webinar By ComplianceOnline
Jun 2012
Practical Issues with Conducting Multi-National Clinical Trials for Medical Device Approval in the US
Jun 2012
Residual Moisture Testing of Lyophilized Products - Webinar By GlobalCompliancePanel
Jun 2012
Effective Corrective and Preventive Actions (CAPA): 10 Steps - Webinar By GlobalCompliancePanel
Jun 2012
Implementing Management Responsibility for Medical Devices - Webinar By GlobalCompliancePanel
Jun 2012
The 21 Elements of a 510(k) - Webinar By ComplianceOnline
Jun 2012
Excel Spreadsheet Validation To Eliminate 483s - Webinar by GlobalCompliancePanel
Jun 2012
What Are the Current Tools and Best Techniques for (Clinical Trial) Audit/Inspection Preparedness?
May 2012
Preparing for FDA Inspection and Handling the Consequences
May 2012
An Overview of Risk Management and Risk Analysis Techniques in Clinical Trials
May 2012
Validation of Analytical Methods for FDA Compliance: Step-by-Step - Webinar By GlobalCompliancePanel
May 2012
Water System Biofilm Control and Microbial Monitoring Myths - Webinar By GlobalCompliancePanel
May 2012
FDA Concerns on Alarm Standards and Safety
May 2012
Efficient Computer System Validation - 10 Easy Steps - Webinar By GlobalCompliancePanel
May 2012
Equipment Calibration in FDA QSR – Regulations and Warning Letters
May 2012
Integrating Clinical Evaluation and Risk Management
May 2012
Establishing and following Good Clinical Practice (GCP) compliant with the FDA requirements
May 2012
South Korea: Navigating the Clinical Trial and Regulatory Environment - Webinar By GlobalCompliancePanel
May 2012
How to Survive FDA`s `New` Inspection and Enforcement Practices
Apr 2012
The Hero of Manufacturing Contamination Control - The Microbiology Lab
Apr 2012
Lean Project Management For U.S. FDA-Regulated Industries
Apr 2012
Off Label Product Use Discussions in Social Media
Apr 2012
Issue Detection and Escalation in Clinical Trial Settings
Apr 2012
Good Documentation Practices for GXPs
Apr 2012
Making Risk-Benefit Decisions – Preparing for the New FDA Guidance Documents
Apr 2012
Validation and Use of Excel Spreadsheets in Regulated Environments
Apr 2012
Medical Device Risk Management Using ISO 14971
Mar 2012
Elegant Quality Assurance Practices for Device Efficacy and Efficiency Requirements
Mar 2012
How To Establish An Effective Good Clinical Practice in Drugs and Medical Devices
Mar 2012
Implementing the New USP Chapter <1224> for Analytical Method Transfer
Mar 2012
Business Process Optimization in Pharmacovigilance - Webinar By GlobalCompliancePanel
Mar 2012
Validation of Bioanalytical Methods and Procedures for FDA Compliance
Mar 2012
Changes in the EU Medical Device Directives; 2010 Modifications and the Recast of the MDD Directives - Webinar By GlobalCompliancePanel
Mar 2012
Method Validation in Drug Development Process - Common Mistakes and Issues
Mar 2012
Audit/Inspection Preparedness for Clinical Research/Site Coordinators
Mar 2012
Validation of Analytical Procedures for Use in the Pharmaceutical Industry
Feb 2012
Leaping into Lab: Everything about Waived Testing
Feb 2012
Submission Documentation for Sterilization Process Validation - A Comprehensive View of Content for an Approvable CMC Section
Feb 2012
Implement a Tougher Supplier Audit Program - Webinar By GlobalCompliancePanel
Feb 2012
FDA/EU Compliant Training for Laboratory Personnel
Feb 2012
Quality System Approach and Risk Management for Clinical Trials
Feb 2012
FDA’s Current Thinking for Industry cGMPs for Phase 1 INDs
Feb 2012
Does your pharmaceutical lab have GMP and non-GMP functions?
Feb 2012
Annual Best Practice Phase IV studies
Feb 2012
Live Web Seminar Dietary Supplement Regulatory Compliance in the United States: Labeling, Product Claims & Updates from the FDA By compliance2go
Feb 2012
Solutions for Addressing Fungal and Bacterial Spore Outbreaks in Pharmaceutical, Biotech, and Medical Device Operations
Feb 2012
How to prepare for and survive a CLIA inspection - Clinical Laboratories Improvement Act
Feb 2012
Introduction to the Electronic Common Technical Document
Jan 2012
Analytical Procedures and Procedures Transfer
Jan 2012
Preparing for FDA GCP Inspections – Essentials for Sponsor Companies
Jan 2012
Live Web Seminar Design Controls: What to know when it comes to FDA regulated industry? By compliance2go
Jan 2012
Quality by Design (QbD) for Development and Validation of Analytical Methods
Jan 2012
New Dietary Ingredients in the Regulatory Scheme
Jan 2012
Troubleshooting Microbial Excursions in Pharmaceutical and Biotech Operations
Jan 2012
An Introduction to the FDA New Drug Approval Process
Jan 2012
Live Web Seminar China: Compliance Processes for Life Science Products (Company Establishment, Clinical Trials, Registrations, Renewals and Supply Chain Considerations By compliance2go
Jan 2012
FDA Compliant Handling of Out of Trend Results in Pharmaceutical Quality Control
Dec 2011
Proven Root Cause Investigation Techniques for Pharmaceutical Water Systems
Dec 2011
GMP Annual Training
Dec 2011
Lyophilization Process Development and Cycle Design
Nov 2011
Live webinar on GMP Quality Principles Embodied in the FDA`s Quality Systems Approach to the Pharmaceutical GMP`s and ICH Q 10, Pharmaceutical Quality Systems by Compliance2go
Nov 2011
Key Aspects of the Trial Master File and How to Pass FDA Inspection - Webinar By GlobalCompliancePanel
Nov 2011
Treatment Planning Non-Surgical Periodontal Therapy Cases - Webinar By mentorhealth
Nov 2011
Cleanroom & HEPA Filter Testing & Certification: An Owners Guide - Webinar by GlobalCompliancePanel
Nov 2011
Does your Equipment Program Meet Current Regulatory Expectations - Webinar By GlobalCompliancePanel
Oct 2011
Equipment Validation, Tracking, Calibration, and Preventive Maintenance - Webinar By GlobalCompliancePanel
Oct 2011
Live webinar on The FDA Inspection: Preparation, Performance, and Follow-up by compliance2go
Oct 2011
Hybrid Quality Systems For Pharmaceuticals - Combining ICH Q7A & Part 210-211 - Webinar By GlobalCompliancePanel
Sep 2011
Good Laboratory Practice Regulations: Introduction and Strategies for Implementation
Sep 2011
Understanding Risk Management in Medical Devices
Sep 2011
Drug Master Files (DMFs) - Understanding and Meeting Your Global Regulatory and Processing Responsibilities By compliance2go
Sep 2011
Applying GMP Quality Principles to Deviations & Nonconformities and Effective Corrective And Preventive Action Systems-By Howard T. Cooper
Sep 2011
Investigator responsibilities and Legal commitments in Drug and Device Clinical Research
Sep 2011
Applying GMP Quality Principles to Deviations & Nonconformities and Effective Corrective And Preventive Action Systems
Sep 2011
How to design A CAPA System that meets Compliance Requirements
Sep 2011
Ensuring Integrity and Security of Laboratory Data
Sep 2011
Responding to FDA Form 483s and Warning Letters - Webinar By ComplianceOnline
Sep 2011
Common GCP Violations and Site Mistakes - How to Avoid them
Aug 2011
Preparing for an FDA Pre-Approval Inspection - Webinar By ComplianceOnline
Aug 2011
Why Post-market Pharmacovigilance trials are increasingly seen : What do they tell us and why are they important
Aug 2011
How Due Diligence in Accurate Adverse Event Reporting is the Key to a clean FDA Audit
Aug 2011
Clinical Project Management - Webinar By ComplianceOnline
Aug 2011
Vendor Qualification - Designing and Implementing an Efficient and Compliant Vendor Program
Aug 2011
Trial Master File for Research Sites: Can You Pass FDA Inspection?
Aug 2011
Learning from Recent FDA Warning Letters Related to Computer Validation and Part 11
Jul 2011
Vendor Qualification Auditing for FDA Computer System Compliance - Webinar By ComplianceOnline
Jul 2011
DHF, DMR, DHR, Technical File and Design Dossier - Key Requirements and Future Directions - Webinar By GlobalCompliancePanel
Jun 2011
Designing an effective cleaning validation in today`s regulatory environment
Jun 2011
Develop and Execute the Company Software V&V Program - Webinar By GlobalCompliancePanel
Jun 2011
Good Documentation Practices for Laboratory Operations - Webinar By GlobalCompliancePanel
Jun 2011
Sterilization Options for Challenging Products
May 2011
Pharmaceutical and Medical Device Validation Guidance`s - Similarities and Differences - Webinar By GlobalCompliancePanel
May 2011
`The Right Stuff` – Implementing Quality Control Tools in Quality Systems Operations
May 2011
Designing a CAPA System that Meets and Exceeds Regulatory Requirements - Webinar By GlobalCompliancePanel
May 2011
The GCP/ICH Obligations of Sponsors, Monitors, and Investigators - barriers and solution - Webinar By GlobalCompliancePanel
May 2011
FDA Clinical Trial Auditing and the due diligence Companies should conduct as part of their monitoring program - Webinar By GCP
May 2011
Information Security Risk Analysis: Meeting HIPAA Requirements and the Meaningful Use Objective - Webinar By GlobalCompliancePanel
May 2011
FDA`s New Enforcement of 21 CFR Part 11 - Webinar By GlobalCompliancePanel
May 2011
Designing and Implementing the Quality System for Combination Products - Webinar By GlobalCompliancePanel
May 2011
Best Practices for the Implementation and Use of Test Management Tools - Webinar By GlobalCompliancePanel
Apr 2011
Gowning Systems Used in Cleanrooms & Controlled Environments - Webinar By GlobalCompliancePanel
Apr 2011
Avoiding `Failure to Investigate` - Observations by Conducting Effective Investigations
Apr 2011
Proficiency Testing: How to Pass with Flying Colors and What to Do If You Don`t
Apr 2011
Designing appropriate product specifications for lyophilized parenteral products
Apr 2011
Calibration and Qualification in Analytical Laboratories - Webinar By GlobalCompliancePanel
Apr 2011
Preparing for Pre-approval Inspections - Webinar By GlobalCompliancePanel
Apr 2011
The 510(k) Process and Risk Management
Apr 2011
Data Security Analysis for Healthcare Providers - Webinar By GlobalCompliancePanel
Apr 2011
FDA`s Proposed Rule Regarding Device Establishment Registration and Listing and How to Register and List - Webinar By GlobalCompliancePanel
Apr 2011
Understanding Attribute Acceptance Sampling including Z1.4 and c=0 Plans - Webinar By GlobalCompliancePanel
Apr 2011
Elements of the Lot Disposition Process - Webinar By GlobalCompliancePanel
Apr 2011
FDA`s Revised 510(k) Premarket Notification Process
Apr 2011
ComplianceOnline Webinar - Why and How - Verification of Compendial Methods - USP [1226]
Apr 2011
Decoding CLIA Regulations: Calibration, Calibration Verification and Method Validation
Apr 2011
Change Control -- Your Company`s GMP Weak Point - Webinar By GlobalCompliancePanel
Apr 2011
Controlled Substances and the Hospital Pharmacy - Webinar By GlobalCompliancePanel
Apr 2011
Understanding the Calibration Curve - Webinar By GlobalCompliancePanel
Mar 2011
A Comparison of the Pharmaceutical and Medical Device Good Manufacturing Practices - A Study of Similarities and Differences - Webinar By GCPanel
Mar 2011
The Pharmaceutical Quality System - Webinar By GlobalCompliancePanel
Mar 2011
Navigating the Regulatory Environment for the Implementation of Alternative Microbiology Technologies - Webinar By GCPanel
Mar 2011
Making Correct Employee- Contractor Classifications
Mar 2011
Meet FDA Expectations for a Tougher Supplier Audit Program - Webinar By GlobalCompliancePanel
Mar 2011
Medical Device Recalls: How to Manage Them and Recent Trends - Webinar By GlobalCompliancePanel
Mar 2011
How to use QSIT to Your Advantage - Webinar By GlobalCompliancePanel
Mar 2011
Off-Label Promotion of Drugs - Regulatory Documents Explained - Webinar By GlobalCompliancePanel
Mar 2011
How to Prevent or Handle Protocol Deviations and Violations to be GCP and Regulatory Compliant?
Mar 2011
Recruiting is Critical to Your Success: What is the Secret - Webinar By GlobalCompliancePanel
Mar 2011
Project Management for Clinical Trials - Webinar By GlobalCompliancePanel
Mar 2011
Food Drug & Cosmetic Act: Implementing Regulations & Major New Laws - An Overview - Webinar By GlobalCompliancePanel
Mar 2011
The Investigation System (Discovery, Planning, Root Cause Analysis, CAPA) - Webinar By GlobalCompliancePanel
Mar 2011
How to reduce EO residuals in medical devices
Feb 2011
Last changes in Canadian ethics regulations for clinical trial
Feb 2011
How to secure GCP compliance in Clinical Trials: The complete overview of the critical parameters 2010
Feb 2011
Practical Laboratory Statistics - Webinar by GlobalCompliancePanel
Feb 2011
Using Foreign Trial Data in Your NDA Approval Process - Webinar By GlobalCompliancePanel
Feb 2011
Eliminate the Confusion –Annex 13 GMP guide
Feb 2011
Responsibilities of a Principal Investigator in Clinical Trials: What you Must Do to Ensure Trial Compliance
Feb 2011
Full Day Virtual Seminar : Annual GLP Refresher Course
Feb 2011
Webinar on Pharmacovigilance Audit - Webinar By GlobalCompliancePanel
Jan 2011
Project Management in a cGMP Environment - Webinar By GlobalCompliancePanel
Jan 2011
Full day Virtual Seminar - Compliance for 21 CFR Part 11, reducing costs using risk-based computer system validation
Jan 2011
How to Vet an IRB: Expose and Fix Problems Before They Threaten Your Trial
Jan 2011
Navigating Pediatric Trials from recruitment to successful on-time completion - Webinar By GlobalCompliancePanel
Jan 2011
Assessing GCP Compliance in Clinical Trial Audits- Risk management and Best practices - ComplianceOnline Clinical Training
Dec 2010
Laboratory Investigations Relating to Sample Re-Analysis: Covering the basics before being called out - ComplianceOnline Laboratory Webinar
Nov 2010
How to Use Foreign Trial Data in Your NDA Approval Process
Nov 2010
Are you a new Clinical Research Coordinator? Tips on how to get started, what to expect
Nov 2010
Full Day Virtual Seminar - Reduce Software Validation Costs and Pass the New 21 CFR Part 11 Inspections - by GlobalCompliancePanel
Nov 2010
Full Day Virtual Seminar - Design and Validation of Excel Spreadsheets: Step-by-Step
Oct 2010
ComplianceOnline Virtual Seminar - 21 Cfr Part 11: Complete Manual For Compliance Success
Oct 2010
ComplianceOnline Webinar - Gamma Sterilizer Validation: Method 1 and VDmax25 per ISO 11137 ()
Oct 2010
The Tougher U.S. FDA - One Year Later
Oct 2010
What exactly is required for 21 CFR Part 11 compliance?
Oct 2010
Integrating Clinical Evaluation and Risk Management (ISO 14971)
Oct 2010
Best Practices for Writing an Effective SOP to Lead to Successful FDA Inspections
Oct 2010
The FDA Tripod - Clinical Trial Regulations, Compliance and GCP in Drug Development
Oct 2010
ComplianceOnline Webinar - GMPs in Biopharmaceutical Development Laboratories
Oct 2010
Best Practices for Managing FDA Investigators and Handling FDA 483 Observations
Sep 2010
Ensuring GCP compliance through quality auditing in clinical trial
Sep 2010
Understanding and Preparing for FDA`s New Part 11 Inspection Program
Sep 2010
The ICF Process: Tips on Achieving Optimal compliance and Comprehension
Sep 2010
Quality by Design (QbD) and Analytical Methods - Webinar by GlobalCompliancePanel
Sep 2010
Developing Supplier Quality Auditor Training Programs
Sep 2010
Verification of Pharmacopeia Methods - Webinar by GlobalCompliancePanel
Sep 2010
ComplianceOnline Webinar - Controlling Change to meet GMP Requirements
Sep 2010
Effective & Essential CAPA process to avoid FDA 483 - Webinar by GlobalCompliancePanel
Sep 2010
Good Documentation Practices for GMP Operations - Webinar by GlobalCompliancePanel
Sep 2010
ComplianceOnline Webinar - Streamline Documentation System in Pharmaceutical Laboratory
Aug 2010
Conducting Value Added Audits of Technical Service Providers - Webinar by GlobalCompliancepanel
Aug 2010
Method Transfer of Analytical Methods - Webinar by GlobalCompliancepanel
Aug 2010
System Based Inspections - The Laboratory Control System
Aug 2010

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