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Conferences on Quality assurance in USA (past events)
Tours & Transport
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Event Tickets
Conferences on Quality assurance
USA
(past events)
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Showing 218 conferences
Agile Testing Days USA
Jun 2024
Clinical Quality Oversight
May 2024
STAR East
May 2024
Project Control Summit
May 2024
Warranty Chain Management Conference (WCM)
Dec 2023
The American Conference on Clinical Trials & Regulation of Medical Devices (CTRMD)
Nov 2023
Live Exchange Conference
Nov 2023
mRNA Quality Control and Comparability Summit
Jun 2023
Raw Material Requirements (Health Canada/USP/EP) in a cGMP Environment - Issues and Solutions
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
eCTD Submissions of IND and NDA/BLA to the US FDA, EU and Canada
Nov 2019
Effective Quality Oversight of Pharmaceutical Contract Manufacturing Organizations (CMOs)
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
Packaging and Labeling in Pharmaceutical Production
Jul 2019
HEDIS & Quality Improvement Forum
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
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
The Life Cycle Approach to Cleaning Validation
Dec 2018
TMF Plus and eCTD Plus
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
21 CFR Part 11 Compliance for Computer Systems Regulated by FDA
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
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
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
eCTD Submissions of IND/NDA to the US FDA, EU and Canada
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
Data Integrity, 21 CFR 11 & Annex 11 Implementation
Dec 2017
Applied Statistics, with Emphasis on Risk Management in R&D, QA/QC, and Manufacturing
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
Workshop by Former SEC Inspector General: How to Conduct Internal Fraud Investigations & Effective Reporting
Aug 2017
How to prepare a 510(k) Notification and a Technical File for the CE Mark
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
Risk Analysis and Design of Experiments (DOE) in Process Validation and Development
Oct 2016
Supplier and Contractor Qualification and Control:
Oct 2016
FDA`s Regulation of Implantable and Wearable Sensors
Oct 2016
Advertising and Promotion of Dietary Supplements
Oct 2016
Human Error Reduction Model: How to Manage Human Performance Deviations in a Regulated Environment
Sep 2016
How to Preventing Root Cause and Conduct Analysis for Corrective Action after an Incident or Non-conformance
Sep 2016
How to Perform a Cognitive Load Assessment for Human Error Reduction
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
The Magic of Conflict
Aug 2016
Building a Vendor Qualification Program for FDA Regulated Industries
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
Food Safety Compliance & Risk
Sep 2011
CPI for Defense and Government
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
Warranty Chain Management Conference
Mar 2011
Predictive Analytics World Workshop-Hands-On Predictive Analytics
Mar 2011
Clinical Supply Chain Optimization
Mar 2011
Predictive Analytics World Workshops-The Best and the Worst of Predictive Analytics
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
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