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ComplianceOnline
Conferences on Quality assurance (past events)

ComplianceOnline organizes international conferences, seminars, workshops and other events in various fields, including business, education, government, global issues, health, medicine, industry, lifestyle and science....

ComplianceOnline has a presence in more than 20 countries around the world, including, Australia, Austria, Bangladesh, Brazil, China, Ireland and Kuwait.

ComplianceOnline hosts events on a wide range of topics, such as Aerospace, Agriculture, Alternative medicine, Anaesthesiology, Architecture, Interior design, Artificial Intelligence (AI) and Banking, among others. The events are designed to provide a platform for professionals and others to exchange knowledge, network, discuss new developments in respective fields as well as showcase products and services to a targeted audience.

Related topics
Showing 271 conferences
Audits - Self/Internal, Vendor and Regulatory Inspections
Nov 2024
The ACH Network - Electronic Payments in Detail, ACH 101, ACH 201, and ACH 301
Oct 2024
Statistical Analysis for Process and Product Development
May 2023
Quality Control Laboratory Compliance - cGMPs and GLPs
Apr 2023
Statistical Elements of Implementing ICH Quality Guidelines
Mar 2023
Statistics for Process Control
Feb 2023
Risk Management in Medical Devices Industry
Jun 2021
FDA Audit, Quality Assurance Practices, Responsibilities and Expectations
Sep 2020
Investigational New Drug (IND) & Investigational Device Exemptions (IDE) Applications Preparation and Submission, and Conducting FDA Meetings
Jun 2020
Normality Tests and Normality Transformations: Explanations, Justifications, and Uses
Jun 2020
The Difference Between Food Safety and Branding Decisions
Jun 2020
Technical Writing for Pharma, Biotech and Med Devices
Jun 2020
Pharmaceutical Quality Management System (GMP Requirements, ICH Guidance, QbD, and USFDA/EMA Regulations)
Apr 2020
Quality and GMP Compliance for Virtual Companies (Pharmaceutical, Medical Device & Biologics Industries)
Feb 2020
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
eCTD Submissions of IND and NDA/BLA to the US FDA, EU and Canada
Nov 2019
Applying ISO14971 / IEC62304 / IEC62366-1 - A Practical Guide On How To Implement Risk Management
Nov 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
Good Documentation Practice (GDocP) for FDA Regulated Industry
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
Drug Master Files (DMF) - Translating FDA Guidances into usable documentation
Jul 2019
Root Cause Analysis - Starting at the Beginning
Jul 2019
Implementation and Management of GMP Data Integrity
Jul 2019
Information – Governance, Risk, Compliance
Jun 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
Using Kanban JIT Systems to Run a Startup Plant
Jun 2019
Statistical Process and Quality Control
Jun 2019
FDA`s Expectations from Supplier Management for GMP: Quality Agreements and More
Jun 2019
Lyophilization Process Development and Cycle Design with a Case Study
Jun 2019
Risk-Based Verification and Validation Planning to Meet US FDA and ISO 13485 Requirements
Jun 2019
U.S. Adverse Event Reporting Regulations for Drugs, Dietary Supplements and Cosmetics
Jun 2019
How to Conduct Successful Supplier Audits
May 2019
Supplier and Service Provider Controls: FDA Expectations
May 2019
CDISC Mapping 4: SDTMs and ADAMs Examples (80%/20% Mapping Rule)
May 2019
GxP/GMP Requirements and its Consequences for Documentation and Information Technology Systems
May 2019
ICH Q7 FDA Guidance - Its Structure, History, Application and Writer`s Intent
May 2019
New Elemental Impurities Tests for Pharmaceutical Products According to the New ICH Q3D and USP 232/233 Guidelines
May 2019
Supplier Quality Assurance Agreements: Why a General Supply Agreement Not Be Enough with Some Suppliers
May 2019
Storm Water Pollution Prevention Plans (SWPPP)
May 2019
Ethylene Oxide (EO) Sterilization Basics for R&D Engineers
May 2019
Transfer of Analytical Methods according to USP <1224>
May 2019
Statistical Techniques for Medical Device Manufacturers
May 2019
Auditing API Facilities: A MUST to properly prepare for an FDA Regulatory API GMP Inspection
May 2019
Label Claims for food, Probiotics and Cosmetic products in Brazilian Regulatory System
May 2019
How to Ensure Your Foreign Vendors are FDA Compliant: Conducting Vendor Audits, Monitoring, and Using Checklists
May 2019
Pre-Formulation and Formulation Development of Small and Large Molecules for a Lyophilized Product
May 2019
Production and Process Controls - Ensuring your medical device conforms to its specifications
May 2019
Design History Files and Technical Files/Design Dossiers - Meeting U.S. FDA CGMPS and the EU`s MDD Requirements
May 2019
Effective Records Management and Document Control for Medical Devices
May 2019
Stability Studies & Estimating Shelf Life
May 2019
Compliance Measures for Case Managers
May 2019
How to Manage Your Vendors in Clinical Research
Apr 2019
Human Error Investigations, Root Cause Determination and CAPA Effectiveness
Apr 2019
Contemporary Case Management Staffing and Models: Best Practices in the Era of Value-Based Purchasing
Apr 2019
CDISC Mapping 3: Compare and Contrast SDTM and ADaM Steps
Apr 2019
Implementing a Quality Management System
Apr 2019
Estimating Reliability Performance with Accelerated Life Tests
Apr 2019
How to conduct Annual Product Reviews to achieve GMP Compliance
Apr 2019
Complaint Management: Best Practices to Assure Compliance and Customer Retention
Apr 2019
Reprocessing Reusable Medical Devices - Cleaning and Labeling Requirements
Apr 2019
Practical Supplier Control Practices
Apr 2019
Constructing an Effective Argument
Apr 2019
Data Integrity, Good Documentation Practices and Electronic Data Governance
Apr 2019
Method Development and Validation for Assays Supporting Testing of Biologics
Mar 2019
Risk Based Monitoring for GCP Compliance
Mar 2019
How to Implement a Quality Management System According ISO 13485?
Mar 2019
Human Error Reduction in GMP Related Environments
Mar 2019
Medical Device Single Audit Program (MDSAP) - How to implement MDSAP in an existing Quality Management System (QMS)? Medical Device Single Audit Program (MDSAP)
Mar 2019
How to Implement a Quality Management System According ISO 13485?
Mar 2019
Failure Modes and Effects Analysis - An effective Risk Management Tool
Mar 2019
Medical Device Single Audit Program (MDSAP) - How to implement MDSAP in an existing Quality Management System (QMS)?
Mar 2019
How to apply ISO 62304 standard in a medical software development project?
Mar 2019
How to Write Effective 483 and Warning Letter Responses
Mar 2019
FDA Regulations for Environmental Monitoring (EM) Program
Mar 2019
Country of Origin Marking for Imports/Exports
Feb 2019
FDA Compliance and Clinical Trial Computer System Validation
Feb 2019
Human Error and Cognitive Load: How to Reduce Memory and Attention Failures
Feb 2019
Outstanding Leadership Through Social Intelligence
Feb 2019
Introduction to Root Cause Investigation for CAPA
Feb 2019
Statistics for Quality Engineering
Feb 2019
Successful Water System Sanitization
Feb 2019
Hazard Analysis and Product Risk Management Under ISO 14971 and ICH Q9
Feb 2019
Process Capability for Normal and Non-Normal Data
Feb 2019
Understanding FDA Design Verification and Validation Requirements for Medical Devices
Feb 2019
Confidence/Reliability Calculations of Product and Product Capability
Feb 2019
Complaint Handling, MDR`s & Recalls
Feb 2019
Achieving Success and Compliance in the Supply Chain
Feb 2019
ASTM 2500: Lessons Learned Through a Decade of Implementation
Feb 2019
How to Develop, Implement and Manage an Effective Change Control Program
Jan 2019
Risk Based Approaches for Clinical Trials
Jan 2019
ISO 13485:2016 - What are the hot topics and changes?
Jan 2019
Translating Academic Assays for GLP Use
Jan 2019
Validation Master Plan - The Unwritten Requirements
Jan 2019
How to Prepare for an FDA Inspections?
Jan 2019
Medical Marijuana in the Workplace
Jan 2019
Vendor and Supplier Qualification Program for FDA Regulated Industries
Dec 2018
The Life Cycle Approach to Cleaning Validation
Dec 2018
Meet the Tougher U.S. FDA CGMPs
Nov 2018
Ensuring Integrity and Security of Laboratory Data
Nov 2018
Data Analysis in QSR - Techniques and Tools to avoid Warning Letter
Nov 2018
Requirements for IQ, OQ and PQ Quality Protocols
Oct 2018
Introduction to Design of Experiments
Oct 2018
Good Documentation Practice and Record Keeping Regulations (FDA & EMA)
Oct 2018
Troubleshooting Ethylene Oxide (EO) Processes
Oct 2018
Recent FDA Auditing Practices and the Top 10 Most Common Cited GMP Deficiencies
Sep 2018
CGMP controlled Raw Materials
Sep 2018
The Regulatory Expectations for Environmental Monitoring Programs
Aug 2018
Statistical Analysis for Product Development
Jul 2018
Laboratory Investigations for Out of Specification Results
Jul 2018
Good Documentation Guideline (Chapter <1029> USP)
Jul 2018
Root Cause Analysis (RCA) in the Laboratory - Addressing Non-Conformances
Jul 2018
How to Make Sure Your Foreign Vendors are FDA Compliant and Stay that Way
Jul 2018
Internal GMP Audit Program - Execution and Communication
Jul 2018
Develop a Compliant Validation Protocol and Analytical Procedures according to the FDA Guidance and USP Good Documentation Practices
Jul 2018
Developing a HACCP program that is effective, appropriate and compliant
Jul 2018
Biocompatibility Testing; what you need to know
Jun 2018
Overview of Medical Device Regulation in Europe
Jun 2018
Approaching unknown cause laboratory investigations using lean tools
Jun 2018
Stability Programs for Leachable Impurities
Jun 2018
Validation of GC/ GC-MS Methodologies
Jun 2018
Document Control and Change Control Process in GxP/GMP Environment
Jun 2018
Current Regulatory Requirements for Sterile Products
May 2018
Does your QC lab do GMP and non-GMP activities?
May 2018
Good Pharmacovigilance Practices in day-to-day Pharmacovigilance
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
Navigating the Maze for Post-Market Compliance -- Complaint Handling, MDRs, Recalls and Proposed Guidance on FDA Risk Benefits
Oct 2017
The Development and Implementation of a Robust Food Safety, Defense and Quality Assurance System
Oct 2017
Pharmaceutical Quality Management System (GMP Requirements, ICH Guidance, QbD, and USFDA/EMA Regulations)
Oct 2017
FDA Scrutiny of Promotion and Advertising Practices
Sep 2017
21 CFR (Codigo de Regulamentos Federais) Parte 11 conformidade para a validacao de software e SaaS (Software como Servico)/Cloud
Sep 2017
World Class Risk Management - What The Best International Standards Say About Risk - ISO 31000, ISO 14971 and ICH Q9
Sep 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
Auditing for Medical Device and Pharma Companies – A Tool to Reduce Quality and Compliance Risk
May 2017
Efficient Process Validation Strategies and Validation Master Plan (VMPs) for Medical Devices
May 2017
Data Integrity: FDA/EMA/TGA Requirements and Implementation
May 2017
How to Write Error Free Procedures and Instructions
Oct 2016
Supplier and Contractor Qualification and Control:
Oct 2016
Advertising and Promotion of Dietary Supplements
Oct 2016
FDA`s Regulation of Implantable and Wearable Sensors
Oct 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
21 CFR Part 11/Annex 11 compliance for software validation and SaaS
Sep 2016
Regulatory Requirements and Principles for Cleaning Validation
Sep 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
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
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
Building a Sustainable Validation Program from Top to Bottom
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
Project management tools to improve productivity and compliance in Analytical laboratories
Feb 2016
Building a Vendor Qualification Program for FDA Regulated Industries
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
Conducting Effective Quality Audits: Beyond Audit Checklists
Sep 2015
Applying Statistical Process Control Effectively
Aug 2015
Supplier Quality Agreements - Essential for Suppliers of Many Outsourced Processes
Aug 2015
Quality Management, GMP and Regulations - Impact on Food, Seafood and Nutritional Supplements
Jul 2015
A Risk-Based Methodology to Develop and Prepare an Effective Service Level Agreement (SLA) Package to Improve Service and Security Quality
Jul 2015
Preparing for the LDT Regulation
Jul 2015
The European Clinical Trial Directive…Plus…European Filings and Registration Procedures
Jun 2015
Reduce the Risks of Foreign Material Contamination
Apr 2015
UDI Implementation
Apr 2015
Is it Method Verification or Validation, or Just Semantics?
Apr 2015
Application of Disinfectants and Sterilants to Control Microorganisms; FDA Endotoxin Test – Understanding the Latest Revision
Mar 2015
Auditing for Microbiological Aspects of Pharmaceutical and Biopharmaceutical Manufacturing
Feb 2015
Conducting Effective Investigation of Out-of-Specs and Atypical Laboratory Data
Jul 2014
Understanding ISO 13485 vs. ISO 9001 for Successful QMS in Medical Device Industries
Mar 2014
Implementing a Quality Program Using Compliance Measures With a Focus on Key Steps to Pass an ISO External Audit
Feb 2014
Supplier Quality Agreements for Medical Devices
Nov 2013
Water System Mythology: Common False Beliefs for Microbial Control and Monitoring
Oct 2013
Risk Management for Medical Devices: ISO 14971:2007
Oct 2013
How to Withstand an FDA Audit of your Facility
Apr 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
How to Prevent or Handle Protocol Deviations and Violations to be GCP and Regulatory Compliant
Mar 2013
Auditing Technology and IT Investment Management
Feb 2013
Immunogenicity to biologics: processes, impact on efficacy and safety, and management strategy
Feb 2013
The Toolbox for CAPA and Risk Management
Jan 2013
FAA (SMS) - Implementation Guidance for Equipment/Service Providers
Jan 2013
Pharma and Biopharma Quality System Refresher Course
Jan 2013
Statistics in Quality Control: Critical Decisions - Risks & Basics
Dec 2012
Efficient, Effective and Compliant Documentation in the QC Laboratory
Nov 2012
Introduction to Biotechnology Analytical Methods
Oct 2012
Basic and Advanced Quality Tools: What Every Quality Professional Should Know?
Oct 2012
(QMS) Competence and Training Requirements per FDA QSR and ISO 13485
Aug 2012
Process Validation - Webinar By ComplianceOnline
Jun 2012
Service Level Agreements (SLAs) - Preparation Guidelines for Effective SLAs - Webinar By ComplianceOnline
Jun 2012
The Hero of Manufacturing Contamination Control - The Microbiology Lab
Apr 2012
Lean Project Management For U.S. FDA-Regulated Industries
Apr 2012
Modeling and Optimizing Process Behavior using Design of Experiments
Apr 2012
Making Risk-Benefit Decisions – Preparing for the New FDA Guidance Documents
Apr 2012
Validation of Bioanalytical Methods and Procedures for FDA Compliance
Mar 2012
Predicting Warranty Expense Using Reliability Analysis Methods
Mar 2012
Validation of Analytical Procedures for Use in the Pharmaceutical Industry
Feb 2012
Does your pharmaceutical lab have GMP and non-GMP functions?
Feb 2012
Setting up an effective Internal Audit Program
Feb 2012
The Odds are Against Auditing: Statistical Sampling in Audit
Jan 2012
Record Keeping for a (Food) Recall: Keeping Records to Minimize the Affect of a Recall
Jan 2012
How to Audit remotely using Online Auditing Techniques
Jan 2012
NLEA Regulation for Retail and Foodservice Labeling - Government Mandate and Additional Verbiage to Increase Food Safety and Brand Protection
Jan 2012
`The Right Stuff` – Implementing Quality Control Tools in Quality Systems Operations
May 2011
Lyophilization Process Development and Cycle Design
May 2011
Designing appropriate product specifications for lyophilized parenteral products
Apr 2011
An Advanced course on Lean Documents and Document Control
Apr 2011
US FDA requirements for food contact packaging material compliance
Apr 2011
ComplianceOnline Webinar - Why and How - Verification of Compendial Methods - USP [1226]
Apr 2011
2-day In-person Seminar - Electronic Records: Effective Approaches that Reduce Costs
Mar 2011
Design Control Explained - Medical Device Webinar
Mar 2011
21 CFR Part 11 Compliance; specifics needed to eliminate 483s
Feb 2011
Integrating a Quality Management System and Risk Management for Medical Devices
Feb 2011
21 CFR Part 212: Quality Systems to Ensure cGMP Compliance
Feb 2011
How to transfer QC procedures for commercial products in pharma industry - ICH and USP guidelines
Feb 2011
Design Validation Protocol and Acceptance Criteria for Chromatographic Methods to meet ICH requirements 2010
Jan 2011
The Auditee Bill of Rights - ComplianceOnline Quality Management Webinar
Jan 2011
Establishing Global Drug Substance and Drug Product Specifications – What the Guidelines Don’t Tell You
Jan 2011
Quality and Food safety - Problem Solving Methods (Steps, Tools & Success Key Factors) - ComplianceOnline Food Safety Webinar
Jan 2011
Auditing for Virtual Team Issue Escalation and Problem-Solving in global environment
Jan 2011
Avoiding FDA 483 Observations by Identifying the Root Cause of Deviations
Dec 2010
Food Safety Traceability Systems – recall traceability capabilities, costs and trends - ComplianceOnline Food Safety Webinar
Dec 2010
Recalls of Medical Devices in the US
Dec 2010
The Riskability Integration. – Integrating strategies and HR in EGRCM. Steps to leverage the impact of EGRCM mandates
Dec 2010
QSR Device Inspections – Transition from “Barely Surviving” to “Gaining Control”
Nov 2010
Controlling Change to meet GMP Requirements
Nov 2010
Comparability Protocols (CPs): How and when to use them for POST APPROVAL CHANGES
Oct 2010
ComplianceOnline Virtual Seminar - Effective Corrective and Preventive Actions (CAPA): 10 Steps to Success
Oct 2010
Validation Basics A-Z: Planning, Implementing & Maintaining
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
ComplianceOnline Webinar - Estimating Greenhouse Gas Emissions; Determining Your Carbon Footprint
Oct 2010
The Tougher U.S. FDA - One Year Later
Oct 2010
ComplianceOnline Webinar - Preparing for and handling FDA Laboratory GMP inspections
Oct 2010
ComplianceOnline Webinar - Importance of Method Validation Protocols and components of MVP in the Laboratory
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
Active and Intelligent Packaging Technologies: A Food Safety and Quality Perspective
Oct 2010
Best Practices for Managing FDA Investigators and Handling FDA 483 Observations
Sep 2010
Critical Role of Quality Audit in GxP Compliance & Improvement
Sep 2010
What to Expect in a Food Safety Audit
Sep 2010
Validating Radiation Sterilization for medical device industries
Sep 2010
Understanding and Preparing for FDA`s New Part 11 Inspection Program
Sep 2010
Effective Quality Process Improvement for Medical Device Firms: Don’t get caught managing process through standardized SOP’s
Sep 2010
CAPA for Manufacturing, Financial Service Companies: Get it Right the Time (Efficient Process)
Sep 2010
ComplianceOnline Webinar - Medical Device Changes and The 510(k)
Sep 2010
Developing Supplier Quality Auditor Training Programs
Sep 2010
Medical Devices in the EU: CE Mark and 93/42/EEC Directive
Sep 2010
Risk Assessments - Key to a Viral Safety Management Plan
Sep 2010
Developing an ethylene oxide (EO) sterilization process for a product with limitations
Sep 2010
The role of Analytical Program to Support Drug Development Process
Sep 2010
ComplianceOnline Webinar - Controlling Change to meet GMP Requirements
Sep 2010
Key Factors to Write an Effective Standard Operating Procedure (SOP)
Sep 2010
Improving Sanitation Standard Operating Procedures In the Food Industry
Sep 2010
Product Risk Management - ISO 14971 and ICH Q9
Aug 2010
ComplianceOnline Webinar - Streamline Documentation System in Pharmaceutical Laboratory
Aug 2010
Understanding International Standards for Medical Devices
Aug 2010
Changes to the EU Variation Rules, Classifications and Submittal Requirements
Aug 2010
Document Approval, Control, and Distribution: How to Meet FDA QSR and ISO 13485 Requirements in a Relatively Paper-Free Manner
Aug 2010
Applying HACCP Principles for Food Processors
Aug 2010

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