Conferences on Quality assurance in USA (past events)

Conferences on Quality assurance in USA address pertinent issues, trends, and innovations in the quality assurance field, providing opportunities to exchange ideas, forge partnerships and explore possibilities for growth....

Showing 220 conferences

IEST Technical Meeting (ESTECH)
May 2024

STAR East
May 2024

Project Control Summit
May 2024

Warranty Chain Management Conference (WCM)
Dec 2023

PAT and Real Time Quality
Dec 2023

The American Conference on Clinical Trials & Regulation of Medical Devices (CTRMD)
Nov 2023

Live Exchange Conference
Nov 2023

Food and Beverage (FoodBev) Exchange
Oct 2023

mRNA Quality Control and Comparability Summit
Jun 2023

Test Automation & Digital QA Summit (TAS)
Mar 2023

Statistical Elements of Implementing ICH Quality Guidelines
Mar 2023

Combination Products Summit
Jun 2022

International Symposium Mayo Clinic Model of Care
Oct 2021

FDA Audit, Quality Assurance Practices, Responsibilities and Expectations
Sep 2020

Quality Assurance Masters Training
Aug 2020

Clinical Trials Inspection Readiness Summit
Aug 2020

Investigational New Drug (IND) & Investigational Device Exemptions (IDE) Applications Preparation and Submission, and Conducting FDA Meetings
Jun 2020

Technical Writing for Pharma, Biotech and Med Devices
Jun 2020

Risk Management in Medical Devices Industry
Jun 2020

Product Complaints Forum
Mar 2020

People Analytics & Workforce Planning Conference
Mar 2020

Quality and GMP Compliance for Virtual Companies (Pharmaceutical, Medical Device & Biologics Industries)
Feb 2020

Intelligent Automation Week Nashville
Dec 2019

Effective Quality Oversight of Pharmaceutical Contract Manufacturing Organizations (CMOs)
Nov 2019

eCTD Submissions of IND and NDA/BLA to the US FDA, EU and Canada
Nov 2019

Managing Your Complaints and Obstacles in Post-Market Requirements -- Results from Top Medical Device Observations During an Inspection
Nov 2019

Data Quality Management for Financial Institutions
Oct 2019

Highly Potent Active Pharmaceutical Ingredients USA
Oct 2019

Applying ISO14971 and IEC62304 - A guide to practical Risk Management
Oct 2019

Designing and Sustaining New and Existing Product Stability Testing Program
Sep 2019

Lifecycle Management of Analytical Methods and Procedures - according to new FDA and USP guidelines
Sep 2019

Exploring Data Integrity To Include FDA, WHO and EMA`s Latest Guidance for Industry (/)
Sep 2019

GMP Compliance for Quality Control and Contract Laboratories
Aug 2019

Human Error Reduction Program: How to investigate, predict, prevent, correct & recover from Human Error in the manufacturing floor and GMP environments
Aug 2019

Aseptic Processing Overview and Validation
Jul 2019

HEDIS & Quality Improvement Forum
Jul 2019

Packaging and Labeling in Pharmaceutical Production
Jul 2019

Drug Master Files (DMF) - Translating FDA Guidances into usable documentation
Jul 2019

Effectively Addressing and Remediating FDA`s Form 483 Findings, Warning Letters and Consent Decree Compliance Issues
Jun 2019

Root Cause Analysis and CAPA using 8-D Problem Solving Method
Jun 2019

Project Management in Clinical Research
Jun 2019

Statistical Process and Quality Control
Jun 2019

Slack Product Lead on Product Meets Improv
May 2019

Statistical Techniques for Medical Device Manufacturers
May 2019

FDA and EU Process Validation and Equipment Qualification
Apr 2019

Death by CAPA - Does your CAPA Program need a CAPA
Apr 2019

Investigational New Drug (IND) & Investigational Device Exemptions (IDE) Applications Preparation and Submission, and Conducting FDA Meetings
Apr 2019

Computer System Validation (CSV) and Data Integrity for Clinical Trials Regulated by FDA
Apr 2019

Data Integrity, Quality Metrics and Data Analytics
Apr 2019

Method Development and Validation for Assays Supporting Testing of Biologics
Mar 2019

Pharmacovigilance Audit and Inspection Conference
Mar 2019

GMP Audit of API Manufacturers - From Start to Finish and Then Some!
Mar 2019

Ensuring Your Foreign Vendors are FDA Compliant – Conducting Vendor Audits, Monitoring, and Using Checklists
Mar 2019

Technical Report Writing and Statistical Analysis for the Pharmaceutical Industry
Mar 2019

SOP Writing, Training and Compliance in the Pharmaceutical Industry
Mar 2019

Cleaning Validation Program, Procedures, Principles and Regulatory Requirements
Mar 2019

Analytical Instrument Qualification and Validation – Understanding Use of Excel and FDA Audit Preparation
Feb 2019

Statistics for Quality Engineering
Feb 2019

Statistical Methods for Design Verification, Process Validation, and Process Control
Feb 2019

Vendor and Supplier Qualification Program for FDA Regulated Industries
Dec 2018

TMF Plus and eCTD Plus
Dec 2018

The Life Cycle Approach to Cleaning Validation
Dec 2018

Annual NLS Food Quality Symposium
Dec 2018

Applied Statistics for Scientists and Engineers
Nov 2018

Qualification and Validation of Laboratory Equipment and Systems for Regulated Industries
Nov 2018

Automotive Quality Management
Nov 2018

The Annual HEDIS & Quality Improvement Summit
Oct 2018

LIBS
Oct 2018

Complaint and Recall Management: A Compliant, Lean Program
Oct 2018

GMPs for All Phases - Ensuring GMP Compliance - Workshop by Ex-FDA Official
Oct 2018

21 CFR Part 11 Compliance for Computer Systems Regulated by FDA
Oct 2018

Advanced Quality Auditing – Workshop
Oct 2018

Strategies for Improving Effectiveness and Efficiency of your Quality Management System
Oct 2018

Demystifying the Quality Management System and Controlled Documents
Oct 2018

Annual NLS Food Evolution Summit
Sep 2018

Statistics for Process and Quality Control
Sep 2018

Pharma cGMP Utility Systems Management
Aug 2018

ICH Q11 – API Manufacturing Workshop
Aug 2018

Statistical Analysis for Product Development
Jul 2018

International Conference on Pharmaceutical Auditing
Jun 2018

Product Recalls Forum
May 2018

HR & Workforce Analytics Summit
May 2018

Statistical Sampling Plans - Methods and Applications
Apr 2018

eCTD Submissions of IND/NDA to the US FDA, EU and Canada
Apr 2018

A Risk Based Strategy for the Development & Validation of and Validation of Analytical Methods with a QbD Approach
Apr 2018

Evolution of the Quality Management System - How to go from Surviving to Thriving
Apr 2018

A Risk Based Approach To IT Infrastructure Qualification & Compliance
Mar 2018

A Risk Based Approach To Data Integrity
Feb 2018

Drug Dissolution Testing and Establishing Plasma Drug Levels in Humans
Feb 2018

Statistical Process Control & Process Capability
Feb 2018

Predicting & Improving Product Reliability
Jan 2018

Quality Audits for the Medical Device Industry
Jan 2018

Applied Statistics, with Emphasis on Risk Management in R&D, QA/QC, and Manufacturing
Dec 2017

Data Integrity, 21 CFR 11 & Annex 11 Implementation
Dec 2017

Regulatory Requirements and Principles for Cleaning Validation
Dec 2017

Quality by Design using Design of Experiments (QbD)
Dec 2017

Implementing ISO 13485:2016
Nov 2017

Compliance Boot Camp
Nov 2017

Supplier Management for Medical Device Manufacturers
Nov 2017

Statistical Methods A Visual Approach
Nov 2017

Global Summit on Food Processing, Safety & Technology
Nov 2017

Navigating the Maze for Post-Market Compliance -- Complaint Handling, MDRs, Recalls and Proposed Guidance on FDA Risk Benefits
Oct 2017

CCW Conference and Expo Fall
Oct 2017

Validation, Verification and Transfer of Analytical Methods (Understanding and implementing guidelines from FDA/EMA, USP and ICH)
Oct 2017

The Development and Implementation of a Robust Food Safety, Defense and Quality Assurance System
Oct 2017

Design Controls for Medical Devices - Regulations, Myths, Challenges, and Best Practices
Oct 2017

Text Analytics World
Sep 2017

FDA Scrutiny of Promotion and Advertising Practices
Sep 2017

World of Transmission & Distribution Asset Analytics Summit
Sep 2017

Validation of Computer Systems for Quality and Software Embedded Medical Devices
Sep 2017

World Class Risk Management - What The Best International Standards Say About Risk - ISO 31000, ISO 14971 and ICH Q9
Sep 2017

Acceptance Sampling - Methods and Applications
Aug 2017

Root cause analysis and CAPA using 8-D Problem Solving method
Aug 2017

Advancing Field Technology
Aug 2017

The Challenges of an Effective Change Control Program and How to Address OOS Results
Aug 2017

How to prepare a 510(k) Notification and a Technical File for the CE Mark
Aug 2017

Workshop by Former SEC Inspector General: How to Conduct Internal Fraud Investigations & Effective Reporting
Aug 2017

Post-Compliance Medical Device Regulations and Evolving Reporting Requirements: Complaint Handling, Medical Device Reporting/ eMDR and Recalls and their compliance with UDI`s
Jul 2017

Quality Management Systems that Comply with ISO13485: 2016
Jul 2017

Auditing for Medical Device and Pharma Companies – A Tool to Reduce Quality and Compliance Risk
May 2017

Cold Chain GDP & Temperature Management Logistics Global Forum - Spring
May 2017

Data Integrity for Clinical Research Summit
May 2017

Efficient Process Validation Strategies and Validation Master Plan (VMPs) for Medical Devices
May 2017

Predictive Analytics World San Francisco
May 2017

Audit Like the FDA - What you need to know for a Audit Like the FDA
May 2017

Predictive Analytics World for Workforce
Mar 2017

Quality Audits for the Medical Device Industry
Mar 2017

FDA Concepts for Medical Device Companies - Regulations, Myths, Challenges, and Best Practices – GlobalCompliancePanel
Dec 2016

Effective and Efficient Internal and Supplier Quality System Auditing for Medical Devices
Nov 2016

Design of Experiments for Process/Product Optimization
Nov 2016

Applied Statistics, with Emphasis on Verification, Validation, and Risk Management, in R&D, Manufacturing, and QA/QC
Nov 2016

MACRA & Quality Payment Program Implementation Forum
Oct 2016

Design Controls for Medical Devices - Regulations, Myths, Challenges, and Best Practices
Oct 2016

How to Write Error Free Procedures and Instructions
Oct 2016

FDA Inspection: Do`s and Don`ts
Oct 2016

Supplier and Contractor Qualification and Control:
Oct 2016

Risk Analysis and Design of Experiments (DOE) in Process Validation and Development
Oct 2016

Advertising and Promotion of Dietary Supplements
Oct 2016

FDA`s Regulation of Implantable and Wearable Sensors
Oct 2016

Human Error Reduction Model: How to Manage Human Performance Deviations in a Regulated Environment
Sep 2016

How to Perform a Cognitive Load Assessment for Human Error Reduction
Sep 2016

How to Preventing Root Cause and Conduct Analysis for Corrective Action after an Incident or Non-conformance
Sep 2016

Using lineament analysis in geological exploration
Sep 2016

Implementing ISO 13485:
Sep 2016

Annual Design Thinking for Banking & Financial Institutions
Sep 2016

21 CFR Part 11/Annex 11 compliance for software validation and SaaS
Sep 2016

Regulatory Requirements and Principles for Cleaning Validation
Sep 2016

Supplier Management for Medical Device Manufacturers
Sep 2016

Statistical Analysis for Process and Product Development
Aug 2016

How FDA Trains Its Investigators to Review Sub-Systems for State of Compliance: What You Need to Do to Prepare for a Successful Inspection
Aug 2016

Building a Vendor Qualification Program for FDA Regulated Industries
Aug 2016

The Magic of Conflict
Aug 2016

Statistical Methods for Product and Process Development
Aug 2016

FDA Scrutiny of Purchasing/Supplier Controls
Aug 2016

Navigating through Maze of In-vitro Diagnostics (IVD) Regulations: A systematic approach from Regulatory Strategy to Regulatory Approvals in U.S./Europe/Canada
Jul 2016

Designing a Supplier Qualification Program
Jul 2016

Predicting & Improving Product Reliability
Jul 2016

BioLogistics Summit
Jun 2016

Implementing an Effective Operational Risk Management Program
Jun 2016

Best Practices for Safety Reporting in Clinical Trials for Drugs, Biologics and Medical Devices
Jun 2016

Fundamentals of Statistical Process Control: Implementation and Assurance of SPC
Jun 2016

Internal Auditing for the Medical Device Industry
May 2016

Verification and Validation Symposium (V&V)
May 2016

Building a Sustainable Validation Program from Top to Bottom
May 2016

Analytical Instrument Qualification and Validation: Understanding to Prepare for FDA Audits to become Part 11 Compliant
May 2016

Integration of Human Factors into Medical Device Design: FDA and European Commission
Apr 2016

Process Validation for Medical Devices: 2-day In-person Seminar
Mar 2016

Unleashing Innovation Summit, New York
Mar 2016

Project management tools to improve productivity and compliance in Analytical laboratories
Feb 2016

Signal Detection, Root Cause Analysis and CAPA Summit
Jan 2016

Equipment, Facility, and Process Qualification and Validation - A Simple Top to Bottom Sustainable Approach
Dec 2015

Account Support Boot Camp
Nov 2015

Pharmaceutical Packaging & Labeling Forum
Nov 2015

Advanced Certified Sustainability (CSR) Practitioner Training (IEMA Approved)
Nov 2015

Developing an Environmental Monitoring Strategy for a Non-Sterile and Aseptic Processing Area (Controlled/Classified Environment) -- To Include HVAC and Utility Systems
Oct 2015

Laboratory Inspections – Be Prepared, Be Validated and Avoid Observations
Oct 2015

Quality Management, GMP and Regulations - Impact on Food, Seafood and Nutritional Supplements
Jul 2015

Problem Solving and Root Cause Analysis - the Key to an Effective CAPA System
Jul 2015

The European Clinical Trial Directive…Plus…European Filings and Registration Procedures
Jun 2015

Quality Assurance for Microbiological Laboratories
Jun 2015

Annual Society of Concurrent Product Development (SCPD) Conference
Jun 2015

ASQ Spring Quality Conference
Apr 2015

International Conference on Software Quality (ICSQ)
Mar 2015

Application of Disinfectants and Sterilants to Control Microorganisms; FDA Endotoxin Test – Understanding the Latest Revision
Mar 2015

Data and Analytics in Life Sciences
Jan 2015

Infocast`s Safer Consumer Products Summit
Oct 2014

CAPCon
Oct 2014

Conducting Effective Investigation of Out-of-Specs and Atypical Laboratory Data
Jul 2014

Pharmacovigilance & Risk Management Strategies
May 2014

Rummler Process Methodology (RPM) Seminar
May 2014

Conceptual and Logical Database Modeling
Apr 2014

Security & Compliance by Objects using UML and SysML (PCI DSS, NERC,...)
Apr 2014

Open Data Protocol (OData) Workshop
Mar 2014

Analyzing and Managing Timeliness and Importance in Dynamic Systems, from Sensors to CEO
Feb 2014

Running Your IT Department Like a Business
Feb 2014

Annual Reliability and Maintainability Symposium - Product Quality & Integrity (RAMS)
Jan 2014

ISPE Process Validation Conference
Oct 2013

Quality Conference
Sep 2013

Global Food Safety & Quality Compliance
Jul 2013

PDA/FDA Pharmaceutical Supply Chain Workshop
Jun 2013

Nearshore Nexus
Apr 2013

ATP Innovations in Testing
Feb 2013

Food Technology & Safety Summit
Oct 2012

Quality Expo Texas
Mar 2012

Hospital Revenue Cycle Management in the Era of `Affordable Care`
Feb 2012

Process Expo
Nov 2011

Annual South Dakota International Business Conference
Oct 2011

CPI for Defense and Government
Sep 2011

Food Safety Compliance & Risk
Sep 2011

Annual Cold Chain Management for Food & Beverage
Jul 2011

2-day In-person Seminar - Electronic Records: Effective Approaches that Reduce Costs
Mar 2011

Predictive Analytics World Workshop-Net Lift Models: Optimizing the Impact of Your Marketing
Mar 2011

Predictive Analytics World Workshop-Hands-On Predictive Analytics
Mar 2011

Warranty Chain Management Conference
Mar 2011

Predictive Analytics World Workshops-The Best and the Worst of Predictive Analytics
Mar 2011

Clinical Supply Chain Optimization
Mar 2011

Integrating a Quality Management System and Risk Management for Medical Devices
Feb 2011

Clinical Trials
Jan 2011

Transportation & Transfer of Biologics & Biological Agents
Dec 2010

Fabtech Int`l & AWS Welding Show
Nov 2010

Conferences on Quality assurance
USA (past events)

Featured Conferences & Exhibitions

The Learning Ideas Conference 2024

FinTech World Forum 2024

ASEAN Circular Plastics Summit 2024

World`s Unmanned Aerial Vehicle Conference

EDULEARN 24 - The 16th annual International Conference on Education and New Learning Technologies

International Academic Conference on Engineering, Robotics, IT and Nanotechnology (IAC-ERITN 2024)

International Academic Conference on Global Education, Teaching and Learning (IAC-GETL 2024)

7th International Congress on Water, Waste and Energy Management (WWEM 2024)

6th International Conference on Green Chemistry and Sustainable Engineering (GREEN 24)

6th Global Conference on Entrepreneurship, Innovation, and Sustainability (GCEIS)

The 3rd International Conference on Materials and Nanomaterials (MNs 2024)

3rd International Conference on Green Energy and Environmental Technology (GEET 24)

TechCon365 Washington, DC

Global Conference on Communication, Business and Technology (Including AI)

Global Conference on Tourism and Hospitality Management

Global Management Conference

14th China International Hair Fair & Salon Show 2024

6th International Workshop on the Theory of Computational Sensing and its applications to Radar, Multimodal Sensing, and Imaging (CoSeRa 2024)

ICERI 2024 - The 17th Annual International Conference of Education, Research and Innovation

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Conferences on Quality assuranceUSA (past events)