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Online Events on Biotechnology (past events)

Online Events on Biotechnology provide opportunities for networking, learning, collaboration, and staying updated with biotechnology advancements, developments, trends and innovations.....

Some of the topics covered in Online Events on Biotechnology are biotech, bioengineering, biomanufacturing, biomedicine, food engineering, bioremediation and biosensors.

Online Events on Biotechnology bring together professionals, researchers, entrepreneurs, and enthusiasts interested in biotechnology topics.

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Showing 474 conferences
International Conference on Biomedicine (ICBM
May 2024
The International Electronic Conference on Biomolecules
Apr 2024
International Conference on Life Sciences (LiSci)
Apr 2024
International conference on Bioinformatics and computational studies (ICBCS)
Apr 2024
Implementation of Single-Use Technology in Biopharmaceutical Production
Mar 2024
Global Meet on Biotechnology and Bioscience (GMBB)
Mar 2024
Fundamentals of Good Manufacturing Practices for Biopharmaceuticals
Feb 2024
International Conference on Vaccines & Infectious Diseases
Feb 2024
International Conference on Clinical Pharmacy and Pharmaceutical Research (ICCPPR)
Dec 2023
GCP Inspection Readiness
Dec 2023
Global Summit on Vaccines Research & Development (GSVRD)
Oct 2023
Global Summit and Expo on Biotechnology and Bioscience (GSEBB)
Oct 2023
Evaluating Biopharma: Continuous Bioprocessing
Oct 2023
Congress of the European Society for Translational Medicine (EUSTM)
Oct 2023
International Conference on Agricultural and Food Science ( ICAFS)
Oct 2023
Smart(er) Biomanufacturing: Evaluating the Risks and Opportunities
Sep 2023
International conference on Orphan Drugs and Rare Diseases
Aug 2023
International Conference on Bioscience & Engineering (BIOSE)
Aug 2023
CFR Part 11 Guidance for Electronic Records and Electronic Signatures in FDA-Regulated Industries
Jun 2023
Purification: New Technologies and Strategies to Support Complex Molecules
Jun 2023
Biodetection Technologies
Jun 2023
Clinical Trials Quality & Inspection Updates
May 2023
Stability & Shelf Life of Biologics
May 2023
Comparability for Biologics
Apr 2023
Antibody Engineering & Therapeutics ASIA
Apr 2023
International Conference on Bioinformatics and Computational Biology (BICoB)
Mar 2023
International Congress on Biomedical and Bio Instrumentation (ICBBI)
Feb 2023
Life Sciences, Clinical Trials, Patient Recruitment & Retention
Jan 2023
Evaluating Biopharma - Gene Therapy Analytics
Jan 2023
Strategy for Cell & Gene Therapies
Jan 2023
Lipid-Based Drug Delivery: Dosage Form Design from Preclinical to -in-Human
Jan 2023
Evaluating Biopharma - Cell Therapy Strategies
Dec 2022
Project Management for Pharma Professionals
Dec 2022
TIGIT Therapies Digital Summit
Dec 2022
International Conference on Advances in Chemical Engineering and Technology
Dec 2022
AI in Clinical R&D Summit
Nov 2022
International Conference on Drug Discovery and Drug Development
Nov 2022
Africa Green Hydrogen Forum
Nov 2022
Global Summit On Medicinal Plants And Natural Products
Oct 2022
International Conference on Material Science and Nanotechnology
Oct 2022
Vaccine Development MasterClass
Oct 2022
International Conference on Nanomedicine and Drug delivery
Sep 2022
Cannabis for the Biotechnology, Pharmaceutical and Nutraceutical Industry MasterClass
Sep 2022
International Conference and Expo on Food Science and Food Safety
Aug 2022
International Conference on Health and Biomedical Science (ICHBS)
Aug 2022
International Summit on Nanomedicine & Nanotechnology
Jul 2022
International Conference on Biomedical Engineering (ICBME)
Jul 2022
Innovative Practices in Technology and Management - International Conference (ICIPTM)
Jul 2022
European Conference on Rare Diseases and Orphan Products (ECRD)
Jul 2022
World Congress on Pharmaceutical Biotechnology
Jun 2022
WITI Summit - Women in Technology
Jun 2022
MENA Pharmacy Congress
Jun 2022
JAK Inhibitors Drug Development Summit
Jun 2022
Medical Writing & Communication Strategy
May 2022
Global Summit on Cancer And Oncology Research
May 2022
Clinical Trial Regulation MasterClass
Apr 2022
Immunogenicity MasterClass
Apr 2022
International Conference on Biomaterials, Cellular and Tissue Engineering
Apr 2022
Sustainable Alternative Materials and Bio-Based Materials Summit
Mar 2022
International Conference on Biofuels and Bioenergy
Mar 2022
International Conference on Clinical Research and Clinical Trials
Mar 2022
Global Webinar on Biosensors and Bioelectronics (GWBB)
Mar 2022
Genetic Vaccine Analytical Development Summit
Feb 2022
International Conference on Biomedical Electronics and Devices (BIODEVICES)
Feb 2022
International Conference on Bioinformatics Models, Methods and Algorithms (BIOINFORMATICS)
Feb 2022
International Joint Conference on Biomedical Engineering Systems and Technologies (BIOSTEC)
Feb 2022
Internationl Conference on BIOIMAGING
Feb 2022
Speaker Programs and Advisory Boards
Jan 2022
International Conference on Bacteriology and Infectious Diseases
Dec 2021
iPSC-Derived Cell Therapies Summit
Dec 2021
World Congress on Cell and Structural Biology
Dec 2021
FDA Pharmaceutical Labeling Boot Camp
Dec 2021
Global Conference on Cleaning Validation
Nov 2021
CMC Readiness Challenge in case of Expedited Programs for Biotechnological Products MasterClass
Nov 2021
World Congress on Human Health Metabolism-Cancer, Obesity, and Diabetes
Nov 2021
Wnt & B-Catenin Targeted Drug Discovery Summit
Nov 2021
Agriculture, Food Science and Technology
Nov 2021
Vendor/CRO Management and Oversight MasterClass
Nov 2021
All you need to know to generated a valuable genetically engineered model
Nov 2021
International Scientific Conference on Probiotics, Prebiotics, Gut Microbiota and Health (IPC)
Oct 2021
International Partnering Conference (BIO-Europe)
Oct 2021
ASHG - American Society of Human Genetics Meeting
Oct 2021
International Conference on Computational Systems-Biology and Bioinformatics (CSBio)
Oct 2021
Leaders in Biobanking Congress
Oct 2021
Temperature Control and Logistics US
Sep 2021
Xcelerate at Biotech Week Boston
Sep 2021
National Institute for Health and Care Excellence (NICE), UK: Transformation in Action
Aug 2021
Congress on Nanomedicine and Drug Delivery
Aug 2021
Patient Recruitment, Engagement and Support Summit
Aug 2021
Congress on Clinical Microbiology and Yeast Congress
Jul 2021
Fresh Produce Shelf Life Extension Technologies Summit
Jul 2021
Global Bioprocessing: Pharma 4.0 Summit
Jun 2021
Continuous Manufacturing Processes for Biotechnological Products MasterClass
Jun 2021
Decoding Digital Health for Life Sciences
Jun 2021
Biologics Formulation Development and Drug Delivery Forum
Jun 2021
Clinical Trial Supply Forum
May 2021
Asia-Pacific Pharma Congress
May 2021
Strategic Alliance Management for Pharma
Apr 2021
Congress on Biomedical Engineering
Apr 2021
Medicinal & Pharmaceutical Sciences Congress
Apr 2021
World Biosimilar Congress USA
Apr 2021
BIO-Europe Spring
Mar 2021
Biotherapeutics Analytical Summit
Mar 2021
Medical Device R&D Summit
Mar 2021
Global Biotechnology Conference
Mar 2021
Ensuring Compliance with Advertising and Promotional Requirements for Drugs and Medical Devices
Mar 2021
World Congress on Clinical Microbiology and Infectious Diseases
Mar 2021
Global Congress on Biotechnology
Mar 2021
The Plant Genomics and Gene Editing Congress Europe
Mar 2021
Scope Summit for Clinical Ops Executives (SCOPE)
Mar 2021
ICMIB: International Conference on Medical Information and Bioengineering
Feb 2021
PepTalk: The Protein Science Week
Jan 2021
World Biomaterials Congress (WBC Virtual)
Dec 2020
World Innovators Meet
Dec 2020
The International Society for Nutraceuticals and Functional Foods (ISNFF) Conference and Exhibition
Nov 2020
International Web Conference on `Recent Trends and Developments in Applied Research and Industrial Practices` (ICRTDARIP)
Nov 2020
Biotechnology Virtual
Nov 2020
Plant Biology Virtual
Nov 2020
Clinical Innovation and Supply Chain Management
Oct 2020
Global Experts Meet on Biotechnology and Biomedical Engineering
Oct 2020
International Food, Nutrition and Bioprocess Technology Conference (Food & Nutrition)
Oct 2020
Psychedelic Drug Development Digital Summit
Oct 2020
BODYNETS - EAI International Conference on Body Area Networks
Oct 2020
Webinar on Biomedical Engineering (iBIOMED)
Oct 2020
D4 Global - Data-Driven Discovery and Development in Pharma R&D
Oct 2020
nanomedicine-pharma
Oct 2020
Global Conference on Stem Cell & Regenerative Medicine
Oct 2020
International Conference on Biomaterials and Biomedical Engineering
Oct 2020
Digital Clinical Biomarkers and World CDx Summit
Oct 2020
World Congress on Biosensors and Bioelectronics
Sep 2020
EuroSciCon Conference on Biotechnology & Bioengineering
Sep 2020
World Congress on Oil Gas Engeineering
Sep 2020
International Conference on Biostatistics and Bioinformatics
Sep 2020
Virtual Conference on Future of Science (SciCon)
Sep 2020
Future Laboratory Informatics
Sep 2020
International Conference on Science & Technology Research (ICSTR London)
Sep 2020
FWD Pharma
Sep 2020
International Conference on Bio-polymers & Polymer Chemistry
Aug 2020
Euro Biosensors and Bioelectronics Conference
Aug 2020
Cancer Genomics Congress: New Era for Cancer Prevention
Jul 2020
International Conference and Expo on Proteomics and Bioinformatics
Jul 2020
International conference on Nanotechnology and Nanomedicine
Jul 2020
International Conference on Food Chemistry, Processed Foods & Toxicology
Jun 2020
Nanomedicine and Nanobiotechnology (iNanomedince)
Jun 2020
International Congress on Pharmaceutical Biotechnology
Jun 2020
Bio International Convention (BIO)
Jun 2020
International Conference on Structural Biology
Jun 2020
International Conference on Advanced Nanoscience and Nanotechnology
Apr 2020
CDISC Mapping 5: ADAM Models - ADSL, BDS and ADAE
Sep 2019
Design of Experiments for Non-Statisticians
Aug 2019
Strategies for Speeding Up Formulation Development
Jul 2019
6 Most Common Problems in FDA Software Validation and Verification
Jul 2019
Assay Validation for Clinical Diagnostics
Jul 2019
Overcoming Obstacles of the Canadian Drug Regulatory Landscape
May 2019
New Elemental Impurities Tests for Pharmaceutical Products According to the New ICH Q3D and USP 232/233 Guidelines
May 2019
Excel Spreadsheets: Develop and Validate for 21 CFR Part 11 Compliance
May 2019
FDA Inspections - Do`s and Don`ts
Mar 2019
Performing an Effective, Robust and Compliant Sterility Failure Investigation: How to Avoid Common Mistakes
Feb 2019
Medical Marijuana in the Workplace
Jan 2019
Verification vs. Validation in Regulated Industries
Jan 2019
Particulates in Biological Products - Evolving Regulations for Testing in Clinical and Commercial Stages
Dec 2018
Validation and Use of Cloud Computing in FDA Regulated Environments
Dec 2018
Ensuring Integrity and Security of Laboratory Data
Nov 2018
Sunshine Act Reporting – Clarification for Clinical Research
Oct 2018
FDA Auditing Practices and the Top 10 Most Common Cited GMP Deficiencies
Oct 2018
Excel Dashboard 101: Time Saving Tactics
Sep 2018
Building a Compliant Documentation and Training System
Aug 2018
Laboratory Investigations for Out of Specification Results
Jul 2018
Root Cause Analysis (RCA) in the Laboratory - Addressing Non-Conformances
Jul 2018
Japan - Regulatory Filing Requirements and Compliance Processes for Life Sciences
Jul 2018
Project Management for FDA-Regulated Companies
Jul 2018
Develop a Compliant Validation Protocol and Analytical Procedures according to the FDA Guidance and USP Good Documentation Practices
Jul 2018
Oversight of CROs-Vendors-CMOs
Jun 2018
Gaining and Re-Establishing Control of Your Cleanroom
May 2018
Document Control and Change Control Process in GxP/GMP Environment
May 2018
Health Product Marketing authorization in Brazil - Documentation, Approval Process, Labeling, Advertising and Post Market Vigilance
May 2018
Analytical Method Validation
Mar 2018
Advances in Food Allergy & Hypersensitivity Research: Triggers and Treatment
Jan 2018
Effective Strategies to Manage Validation In Conformance With The Pharmaceutical Quality System
Dec 2017
Best Practices for an Effective Cleaning Validation Procedures
Sep 2017
How to Prepare for and Host a FDA Inspection and Respond to 483`s
Aug 2017
Statistical Concepts of Process Validation
Jul 2017
Improving Process Stability and Capability - Tips, Traps and Guidance
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
FDA’s 21 CFR Part 11 Add-on Inspections
May 2017
How FDA Trains Its Investigators to Review CAPA, and What You Can do to Prepare
May 2017
TM’s World Molecular & Cell Biology Online Conference
Apr 2017
Good Documentation Practices for FDA-Regulated Computer Systems
Apr 2017
Capturing Justifications in Change Control, Risk Assessment, Validations, and Investigations
Feb 2017
Clinical Trial Monitoring: A Sponsor Responsibility
Feb 2017
Three-dimensional cell culture: Innovations in tissue scaffolds and biomimetic systems
Feb 2017
The Investigational Medicinal Product Dossier (IMPD): EU CTA vs. FDA IND: Comparing the Content and Agency Expectations
Jan 2017
Bacteriophage
Jan 2017
New Technologies Affecting Healthcare
Jan 2017
Effective Corrective and Preventive Action Program (CAPA): The Role of Corrective Action and Preventative Action in Your Quality Management System
Jan 2017
Awareness of Potential Food Safety Problems that Occur During Food Transportation (2)
Dec 2016
Improving techniques and technology for cellular and molecular pathology
Dec 2016
Mandatory GMO Labeling: Preparing for Implementation
Oct 2016
Design and Execution of Stability Studies for Biologics
Oct 2016
Learning Design Controls through Review of FDA 483 Observations
Oct 2016
Production and Process Control: Building a Robust System for Medical Device Companies
Oct 2016
Sub-visible Particulates in Biological products
Sep 2016
Defining and Managing Protocol Deviation/Violation/Exception
Sep 2016
Considerations for a Successful Biosimilars Program
Jul 2016
Biotechnology in Food Processing - How Has it Evolved to Help Us?
Jul 2016
Process Validation - Current Industry Practices and FDA Guidance Document Review
Jul 2016
USP <71> Sterility Testing: New Harmonization with International Compendia and Overview
Jul 2016
Labeling of genetically modified organisms (GMO`s) in the USA
Jun 2016
21 CFR 111 GMP Dietary Supplement Laboratory
Jun 2016
Technical Writing for the Pharmaceutical, Medical Device and Biotech Industries
Jun 2016
Writing Effective Email
Jun 2016
GMP Complaint Systems and Product Recalls
May 2016
Validation of a HPLC/UPLC Methodology
May 2016
How Fixing FDA Compliance Problems (Remediation) Aligns with the 5 Stages of Grief
Apr 2016
Ensuring Compliance of Your Bioanalytical Method Validation with the 2013 FDA Draft Guidance
Mar 2016
Root Cause Analysis - The Heart of a Successful CAPA Program
Feb 2016
Sterilization Processes: The Methods, Parameters and Deficiencies Often Cited
Feb 2016
Creating Effective SOP for Regulatory Compliance
Jan 2016
Payroll Technology
Jan 2016
How to Develop a strong CAPA System by Understanding its Unique Challenges
Jan 2016
Investigational Device Accountability
Jan 2016
Effective Design Controls in Accordance with Subpart C of 21 CFR, Part 820
Jan 2016
Established Condition - The New FDA Guidance
Jan 2016
Drug Master Files: New Implications under GDUFA
Jan 2016
Toyota Kata - Wax On, Wax Off (in partnership with ASQ Lean Enterprise Division)
Jan 2016
U.S. FDA`s Strategic Priorities - and Beyond
Jan 2016
Design Inputs - Design Outputs Traceability Matrix - Principles of Lean Documents and Lean Configuration
Jan 2016
FDA Inspections : Managing the Myth and the Reality
Jan 2016
Risk Management and Risk-Based Monitoring
Jan 2016
Creating and Maintaining a GMP Quality System
Jan 2016
How to Detect Lack of Data Integrity
Jan 2016
FDA`s New Enforcement of 21 CFR Part 11
Jan 2016
FDA Inspection Lessons Learned: Lack of Trial Oversight
Jan 2016
Writing Effective Standard Operating Procedure (SOPs)
Jan 2016
Complaint Handling Requirements - Interrelationship with CAPA, Change Control, Adverse Event Reporting and Recalls, Life Cycle Process Activities
Dec 2015
Objectionable Microorganisms: Considering the Risk
Dec 2015
ICH-FDA Good Clinical Practice – Managing Clinical Trials
Nov 2015
Product Stability Testing Program - Designing and Sustaining New and Existing Programs
Oct 2015
CAPA Training and Causes of Warning Letters due to Lack of Comprehension
Oct 2015
Establishing an FDA-Compliant UDI System
Oct 2015
Orphan Medicinal Product Designation in the EU
Sep 2015
Designing Medical Devices for Long Life at Lower Costs
Sep 2015
Auditing QC and Contract Laboratories for GMP Compliance
Sep 2015
FDA`s enforcement of 21 CFR part 11 compliance
Sep 2015
CAPA Investigations - Tools for a Compliant and Effective Investigation Process
Sep 2015
Meeting Annual U.S. FDA cGMP Training Requirements
Aug 2015
21 CFR Part 820 - Quality System Regulation - Applying Principles of Lean Documents and Configuration
Jul 2015
Software Verification and Validation in Medical Industry
Jun 2015
Writing Evaluation Reports-How to Write Evaluation Report
Jun 2015
Conducting Observational Studies in US, Canada and Europe
Jun 2015
How to Most Effectively Prepare for and Manage FDA Inspection: Best Practices
Jun 2015
The FDA Inspection: Preparation, Management, and Follow-Up
May 2015
Ensuring Data Integrity for FDA/EU Compliance
May 2015
Managing FDA After a Bad Inspection
May 2015
FDA Guidance on RUO (Research Use Only)/IUO (Investigational Use Only) Products
May 2015
South East Asia Regulatory Compliance for Life Science Products - Hong Kong, Taiwan, Thailand, Singapore, Malaysia and Vietnam
Apr 2015
Electronic Records and Signatures - 21 CFR Part 11: Basic Concepts
Apr 2015
Writing and Implementing Statistical Analysis Plans (SAPs) - Domestic and International Guidance under ICH E9
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
Biomedical Software Regulation
Mar 2015
Designing Effective and Efficient Extractables or Leachables Studies for Biologics
Mar 2015
Avoid Warning Letters in View of the U.S. FDA`s Stated Goal
Mar 2015
Current Concepts and Challenges in Cloud Compliance
Mar 2015
Epigenetic Editing - towards reprogramming of gene expression
Mar 2015
Better Alternatives to Sampling Plans
Mar 2015
Metabolic regulation of cell death
Mar 2015
How to Avoid an FDA Warning Letter with a Strong CAPA Program
Mar 2015
Complaint Handling and Management: From Receipt to Trending
Feb 2015
The 6 Most Common Problems in FDA Software Validation and Verification
Feb 2015
DNA methylation changes during cell differentiation
Feb 2015
Auditing for Microbiological Aspects of Pharmaceutical and Biopharmaceutical Manufacturing
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
What is the harm in that? Risk Management 101
Jan 2015
EU Clinical Trial Regulation: New Requirements
Jan 2015
U.S. FDA`s Strategic Priorities - and Beyond
Jan 2015
Developing an Efficient Relationship with FDA
Dec 2014
Clinical Trial Recruitment Methods and Metrics
Dec 2014
FDA Regulations for Food, Drugs, Biologics, Cosmetics, and Medical Devices Including IVDs
Sep 2014
FDA Recordkeeping Requirements
Aug 2014
Controlled Document System for a Life Sciences manufacturing plant utilizing the principles of Lean Documents and Lean Configuration
Aug 2014
FDA’s Part 11 – Enforcement Trends and Affordable Steps to Take Today
Jul 2014
Cleaning, Maintenance and Calibration Programs: Critical Programs but Often Overlooked
Jul 2014
How to Host Regulatory Audits (FDA, EU and Health Canada)
Jul 2014
CAPA Training and Causes of Warning Letters due to Lack of Comprehension
Jul 2014
21 CFR Part 11 Add-On Inspections by the FDA
Jul 2014
Analyzing Your Biggest Data - Practical Text Mining for Regulated Companies
Jul 2014
Basic Components of Establishing Quality Agreements
Jul 2014
Effective Contamination Control in Biopharmaceutical Manufacturing
Jul 2014
Preparing for FDA BIMO Inspection and Management
May 2014
Establishing a Medical Device Complaint Handling System integrated with a UDI System
May 2014
TM`s World Genetics & Genomics Online Conference
May 2014
FDA Warning Letter Close-Out Program
May 2014
Meet FDA Expectations for a Tougher Supplier Audit Program
May 2014
China: Compliance Processes for Life Science Products (Company Establishment, Clinical Trials, Registrations, Renewals and Supply Chain Considerations)
May 2014
The U.S. FDA`s CAPA
Apr 2014
Establishing an Internal Audit Program of the Quality Management Systems Pursuant to ISO 13485 and 21 CFR Part 820
Apr 2014
How To Translate Academic and Discovery Assays Into GLP Compliant Assays
Mar 2014
Ensuring 21 CFR 11 Compliance at Suppliers
Mar 2014
Learning from FDA Warning Letters
Feb 2014
Good Documentation Practices for Clinical Trials
Feb 2014
The Sunshine Act - Are You Prepared? The Reporting Deadline is Approaching Quickly!
Jan 2014
Using SharePoint as a Technology Platform for 21 CFR part 11 - A Case Study
Jan 2014
Clinical Trial Design for Personalised Medicine Webinar
Nov 2013
Remediating Pharmaceutical Water System Biofilm - What to Do After It Gets Ahead of You
Nov 2013
Annual Digital Marketing Strategies for Patient Outreach
Nov 2013
Corrective and Preventive Actions(CAPA) - 8 Steps to Achieve Compliance
Nov 2013
Thorough and Complete Investigations and Follow-up - A Current Regulatory Expectation
Oct 2013
Creating a Good Design History File (DHF) for Audit Success
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
Regulatory Differences Between Biopharmaceutics and Medical Devices
Aug 2013
CAPA – The Heart of Your Quality System
Jul 2013
Supplier Management – Do you comply with the latest FDA and ISO 13485 requirements
Jul 2013
Optimal capacity planning and resource allocation for a portfolio of clinical trials
Jun 2013
The Future of Off-Label Marketing After the Caronia Decision
Jun 2013
FDA and Social Media - How to Promote your Products Using Web 2.0 in Compliance with FDA and FTC Laws and Regulations
Jun 2013
Introduction to Bioequivalence and Therapeutic Equivalence
Jun 2013
Shared facilities and the move to science based risk assessments
Jun 2013
Clinical trial regulations, GCP compliance and FDA inspections
Jun 2013
FDA Warning Letter Closeout Program
May 2013
Complaint Systems – The Essential Requirements
May 2013
Interactive Response Technologies for Clinical Trials
Apr 2013
Container Closure Systems for Liquid and Lyophilized Products
Apr 2013
Auditing the QC Microbiology Laboratory for FDA Compliance
Apr 2013
3-hr Virtual Seminar: Annual ICH GCP Refresher Course
Apr 2013
Design of Experiments in Biotechnology Analytical Development
Apr 2013
When is Corrective Action Not Enough - Doing and Documenting Corrections is an ISO 13485 Expectation
Apr 2013
Bioanalytical Methods Validation
Mar 2013
Defining And Managing User Requirements For Computer System Validation
Mar 2013
Quality Practices for Research and Development (R&D) CMC Laboratories
Mar 2013
Microbiological Risk: Do I Really Need to Test Raw Materials for Microorganisms
Mar 2013
Global Medical Device Reporting - A Comparison of Worldwide Regulations
Mar 2013
Forecasting Clinical Study Enrollment and its Budget Considerations
Mar 2013
21 CFR Part 11 Electronic Records: Electronic Signatures
Mar 2013
Seeking Evidence in Clinical Trials in Hemoglobinopathy
Mar 2013
Electronic Records & Electronic Signatures; 21 CFR Part 11
Mar 2013
Transferring a Medical OEM Molding and Assembly Operation to a Manufacturer With Validated Systems and Processes
Mar 2013
You have a Sterility Failure or Bioburden Excursion - Now What?
Mar 2013
Implementation and Utilization of Standard Operating Procedures (SOPs) at the Clinical Research Site
Mar 2013
Engineering Change Management for Pharmaceutical Capital Projects
Mar 2013
Why are we seeing more Independent Data Safety Monitoring (DMC) use in Clinical Research
Mar 2013
FDA`s 21 CFR 11 Add-On Inspections - Recent Updates
Feb 2013
Advanced Cell Culture & Fermentation - Process Development & Manufacture
Feb 2013
Clinical Study Enrollment Metrics and Their Financial Impacts
Feb 2013
Adaptive Clinical Trials - Clinical Trials Version 2.0
Feb 2013
Effectiveness Measures in CAPA and Risk Management Plans: Applying LSS for Quality Metrics
Feb 2013
Effective CAPA related to Managing Human Error
Feb 2013
Immunogenicity to biologics: processes, impact on efficacy and safety, and management strategy
Feb 2013
Basic Cell Culture & Fermentation - Process Development & Manufacture
Jan 2013
Regulation of Advanced Therapy Medicinal Products in Europe
Jan 2013
Optimal Clinical Supply Planning for Global Drug Development
Jan 2013
Pharma and Biopharma Quality System Refresher Course
Jan 2013
Reducing eDiscovery risk for Pharmaceutical Companies
Dec 2012
Patient Reported Outcomes (PROs): Overview and Guidance for clinical trials and medical product labeling
Dec 2012
Product Hazard Analysis and Risk Management Under ISO 14971 and FDA, ICH Q9
Nov 2012
Introduction to Biotechnology Analytical Methods
Oct 2012
How FDA Trains its Investigators to Review CAPA and What You Should Do to Prepare
Oct 2012
Computer Systems Used in Clinical Trials
Oct 2012
Laboratory Water Systems: Necessary Water Specifications and Validation Challenges
Oct 2012
Clinical Trial Billing - Building a Compliant Process that Works!
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
Hazard Analysis – A practical guide
Sep 2012
How to Select Best Practices a CRO ?
Sep 2012
Stability Studies for Vaccine Products
Sep 2012
Eliminate the Confusion – Analytical Method Qualification and Validation
Sep 2012
Strategies for Preparing and Submitting Successful Citizen Petitions and Suitability Petitions to FDA
Aug 2012
FDA Guidelines on in Class in Man Compounds Targeting Tumor Bioenergetics from Lab Bench to Clinical Trials - Webinar By GlobalCompliancePanel
Aug 2012
Human Behavior in Cleanrooms and Controlled Environments - Webinar By GlobalCompliancePanel
Aug 2012
TM’s world Pathology & diagnosis online conference
Aug 2012
Specialized Formulations – Biomolecules
Jul 2012
Cleanroom Management – From a Microbial Perspective
Jul 2012
Clinical Trial Auditing - Identifying risks and building a more compliant and successful trial
Jul 2012
Recommendations for Cell Banks used in GXP testing - Webinar By ComplianceOnline
Jun 2012
TM’s world Neuroscience online conference
Jun 2012
What Are the Current Tools and Best Techniques for (Clinical Trial) Audit/Inspection Preparedness?
May 2012
An Overview of Risk Management and Risk Analysis Techniques in Clinical Trials
May 2012
Supplier Controls to Meet Tougher U.S. FDA Requirements
May 2012
FDA Concerns on Alarm Standards and Safety
May 2012
Pre-Formulation and Formulation Development of a Sound Bio Pharmaceutical Formulation that is cGMP Compliant
May 2012
TM’s annual world microRNAs and RNAi online symposium
May 2012
Physician Payment Sunshine Act and State Sunshine Law Compliance. Are you Prepared for the New Federal Requirements and Existing State Requirements?
Apr 2012
How to Survive FDA`s `New` Inspection and Enforcement Practices
Apr 2012
FDA Medical Device Regulation for the Beginner
Apr 2012
Conducting EU Studies from a US Virtual Biotech Company
Apr 2012
Acceptance Activities in FDA QSR - Regulations and Warning Letters
Apr 2012
Best Practices for Maintaining an IND and IDE Application with FDA
Mar 2012
Live webinar on Latin America: Regulatory Compliance Requirements for Life Science Products (Focus: Brazil, Mexico, Argentina) By Compliance2go
Mar 2012
Understanding Disinfection and Cleanroom Cleaning in a FDA Regulated Environment
Mar 2012
FDA`s Rules for Financial Disclosure in Clinical Trials Clarified: New Guidance, Practical Application
Mar 2012
Software Verification and Validation Planning and Implementation
Mar 2012
Audit/Inspection Preparedness for Clinical Research/Site Coordinators
Mar 2012
Introduction to the Electronic Common Technical Document
Jan 2012
Preparing for FDA GCP Inspections – Essentials for Sponsor Companies
Jan 2012
Validation and use of Access Databases in FDA regulated environments
Jan 2012
Purposeful Water and Steam System Validation – Not Just A Regulatory Requirement
Jan 2012
SOPs for Clinical Trials – Regulatory Requirement and Key to Effective Management
Jan 2012
Introduction to FDA Good Documentation Practices
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
LIve Webinar on ISO14000: Environmental Management - Ins and Outs of Implementation and Understanding by Compliance2go
Dec 2011
Proven Root Cause Investigation Techniques for Pharmaceutical Water Systems
Dec 2011
Live webinar on Management of Customer Complaints: Receipt, Investigation, and Trending By Compliance2go
Nov 2011
Live webinar on HOW TO PERFORM PROCESS VALIDATION by Compliance2go
Nov 2011
Lyophilization Process Development and Cycle Design
Nov 2011
Live webinar on New Changes to HIPAA Rules - Their expected impact and enforcement schedule By Compliance2go
Nov 2011
Document Approval, Control, and Distribution: How to Develop a Compliant, Cost Effective System By Compliance2go
Nov 2011
Best Practices in Complaint Management - Webinar by GlobalCompliancePanel
Nov 2011
Iraqi Oil Conference (IOC2)
Oct 2011
Live webinar on The FDA Inspection: Preparation, Performance, and Follow-up by compliance2go
Oct 2011
Live webinar on New 21 CFR Part 11 Regulations and How to comply with them by Compliance2go
Oct 2011
FDA`s Draft Guidance on Financial Disclosure by Clinical Investigators - Webinar By GlobalCompliancePanel
Oct 2011
Risk Management during device design according to ISO14971 - Webinar By GlobalCompliancePanel
Oct 2011
Investigator responsibilities and Legal commitments in Drug and Device Clinical Research
Sep 2011
Responding to FDA Form 483s and Warning Letters - Webinar By ComplianceOnline
Sep 2011
Master Validation Planning
Aug 2011
Preparing for an FDA Pre-Approval Inspection - Webinar By ComplianceOnline
Aug 2011
A Simpler Approach to Implementing or Validating CGMPs to 21 CFR 11, Electronic Records, Signatures
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
How to write Standard Operating Procedures (SOPS) & Work Instructions (Wis) that Meet and Exceed Compliance Requirements
Aug 2011
Clinical Project Management - Webinar By ComplianceOnline
Aug 2011
Creation and management of a Controlled Document System for a Life Sciences manufacturing plant utilizing the principles of Lean Documents and Lean Configuration
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
Navigating the new FDA world of Combination Products
Jun 2011
Effective Risk Based Approach to Auditing and Qualifying Suppliers and Vendors - Webinar By GlobalCompliancePanel
Jun 2011
Risk-Based Validation for GxP Facilities - Webinar By GlobalCompliancePanel
Jun 2011
ComplianceOnline Virtual Seminar - Controlling Outsourcing Using Quality Principles - For Lifesciences Companies
May 2011
Retirement of Computer Systems: Strategies for FDA Compliance and Tools for Implementation
May 2011
The GCP/ICH Obligations of Sponsors, Monitors, and Investigators - barriers and solution - Webinar By GlobalCompliancePanel
May 2011
Residual Moisture Testing - Proven Techniques
May 2011
FDA Clinical Trial Auditing and the due diligence Companies should conduct as part of their monitoring program - Webinar By GCP
May 2011
Best Practices for the Implementation and Use of Test Management Tools - Webinar By GlobalCompliancePanel
Apr 2011
Eliminate the Confusion - New Requirements for Clinical Laboratories to Meet GCP
Apr 2011
Vendor/Supplier/CRO Compliance – Lessons Learned & Rules to Live By
Apr 2011
Making Correct Employee- Contractor Classifications
Mar 2011
Why is CAPA so often cited in medical device inspections - Webinar By GlobalCompliancePanel
Feb 2011
Implementation of Rapid Microbiological Methods
Feb 2011
How to secure GCP compliance in Clinical Trials: The complete overview of the critical parameters 2010
Feb 2011
Avoiding FDA 483 Observations by Identifying the Root Cause of Deviations - 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
21 CFR Part 212: Quality Systems to Ensure cGMP Compliance
Feb 2011
Validating Excel and Word Applications Documents - Webinar By GlobalCompliancePanel
Feb 2011
Analytical Instrument and Equipment Qualification in Quality Laboratories - Webinar By GlobalCompliancePanel
Feb 2011
Ethics, Standards and Identifying Risks in Clinical Research - ComplianceOnline Clinical Training
Jan 2011
Medical Device Complaints Handling Strategies for Managing Your Biggest Compliance Challenge
Jan 2011
Assessing FDA’s Proposed Changes to the 510(k) Process in
Jan 2011
Full day Virtual Seminar - Compliance for 21 CFR Part 11, reducing costs using risk-based computer system validation
Jan 2011
Defining and Managing Protocol Deviation/Violation/Exception - Webinar By GlobalCompliancePanel
Jan 2011
Anatomy of a Medical Device Inspection: From EIR to 483 to Warning Letter
Jan 2011
Understanding and Preparing for FDA`s New Part 11 Inspection Program - Webinar By GlobalCompliancePanel
Jan 2011
cGMP: Strategies for implementation and compliance for Phase I Investigational Drug and Biologic products
Jan 2011
How to Vet an IRB: Expose and Fix Problems Before They Threaten Your Trial
Jan 2011
Internal 21CFR Part 11 Compliance Auditing of Computer Systems - Webinar By GlobalCompliancePanel
Jan 2011
Navigating Pediatric Trials from recruitment to successful on-time completion - Webinar By GlobalCompliancePanel
Jan 2011
Solutions for addressing microbial excursions in medical device, pharmaceutical, and biotech industries
Jan 2011
The FDA`s Working Group Reports, I & II - New Directions - Webinar By GlobalCompliancePanel
Dec 2010
Assessing GCP Compliance in Clinical Trial Audits- Risk management and Best practices - ComplianceOnline Clinical Training
Dec 2010
Important requirements when validating sterilizing grade filters - ComplianceOnline Biotechnology Training
Dec 2010
Conducting Clinical Trials in Latin America: keys to successful study implementation
Nov 2010
Performing Investigations for Environmental Excursions - ComplianceOnline Biotechnology Training
Nov 2010
How to Use Foreign Trial Data in Your NDA Approval Process
Nov 2010
The Most Common Problems in FDA Software Validation & Verification - Webinar by GlobalCompliancePanel
Oct 2010
Secrets of an Effective CMC Regulatory Strategy for Biopharmaceuticals Part 1 - Cell Banking - Webinar by GlobalCompliancePanel
Oct 2010
The FDA Tripod - Clinical Trial Regulations, Compliance and GCP in Drug Development
Oct 2010
Ensuring GCP compliance through quality auditing in clinical trial
Sep 2010
The ICF Process: Tips on Achieving Optimal compliance and Comprehension
Sep 2010
Risk Assessments - Key to a Viral Safety Management Plan
Sep 2010
Document Approval, Control, and Distribution: How to Meet FDA QSR and ISO 13485 Requirements in a Relatively Paper-Free Manner
Aug 2010

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