+353-1-416-8900REST OF WORLD
+44-20-3973-8888REST OF WORLD
1-917-300-0470EAST COAST U.S
1-800-526-8630U.S. (TOLL FREE)

Compliance Online - Webinars, Training & Conferences

ComplianceOnline is an industry focused portal, developed for the practitioners of quality and regulatory compliance. They are focused on enhancing global compliance, creating a world where quality and compliance professionals, regulators, and government agencies come together to help the world comply with the intent and the spirit of laws, policies and mandates, ensuring continuous improvement in global operations, quality & safety.

How to Prepare and Submit a Bullet Proof 510(k) Submission - Product Thumbnail Image

How to Prepare and Submit a Bullet Proof 510(k) Submission

  • Training
  • 60 Minutes
  • Global
The Employment Law System and how to stay above the legal line - Product Thumbnail Image

The Employment Law System and how to stay above the legal line

  • Training
  • 60 Minutes
  • Global
The Essentials of Food and Drug Administration Medical Device Regulations:A Primer for Manufacturers and Suppliers - Registration, Medical Device Reporting, Corrections and Removals (Recalls) - Product Thumbnail Image

The Essentials of Food and Drug Administration Medical Device Regulations:A Primer for Manufacturers and Suppliers - Registration, Medical Device Reporting, Corrections and Removals (Recalls)

  • Training
  • 90 Minutes
  • Global
Validation Requirements Based on ICH Q9 - Product Thumbnail Image

Validation Requirements Based on ICH Q9

  • Training
  • 90 Minutes
  • Global
Implementing a GCP Vendor Qualification Program: Ensuring your vendors are in compliance with FDA requirements - Product Thumbnail Image

Implementing a GCP Vendor Qualification Program: Ensuring your vendors are in compliance with FDA requirements

  • Training
  • 75 Minutes
  • Global
Differences in GMP Requirements between Drugs and Biologicals - Product Thumbnail Image

Differences in GMP Requirements between Drugs and Biologicals

  • Training
  • 60 Minutes
  • Global
Quality by Design: what the FDA wants, what you must do, how you can deliver to their expectations and what relief you can expect - Product Thumbnail Image

Quality by Design: what the FDA wants, what you must do, how you can deliver to their expectations and what relief you can expect

  • Training
  • 60 Minutes
  • Global
The Essentials of Food and Drug Administration Medical Device Regulations: A Primer for Manufacturers and Suppliers - Quality System Regulation - Product Thumbnail Image

The Essentials of Food and Drug Administration Medical Device Regulations: A Primer for Manufacturers and Suppliers - Quality System Regulation

  • Training
  • 90 Minutes
  • Global
Risk-Based Software V&V - FDA,GAMP®, 14971 - Product Thumbnail Image

Risk-Based Software V&V - FDA,GAMP®, 14971

  • Training
  • 90 Minutes
  • Global
Monoclonal Antibodies and Therapeutic Proteins: Designing GLP Compliant Nonclinical Programs to Meet FDA Expectations - Product Thumbnail Image

Monoclonal Antibodies and Therapeutic Proteins: Designing GLP Compliant Nonclinical Programs to Meet FDA Expectations

  • Training
  • 60 Minutes
  • Global
IT Infrastructure and Network Qualification- Introduction and Strategies for Compliance and System Uptime - Product Thumbnail Image

IT Infrastructure and Network Qualification- Introduction and Strategies for Compliance and System Uptime

  • Training
  • 60 Minutes
  • Global
Hazard Analysis & Risk Management - New 14971 - Product Thumbnail Image

Hazard Analysis & Risk Management - New 14971

  • Training
  • 90 Minutes
  • Global
Writing Effective Suspicious Activity Reports - Product Thumbnail Image

Writing Effective Suspicious Activity Reports

  • Training
  • 60 Minutes
  • Global
Human Factors Standards and Guidance's for Medical Devices - which documents apply to my situation? - Product Thumbnail Image

Human Factors Standards and Guidance's for Medical Devices - which documents apply to my situation?

  • Training
  • Global
Computer System Auditing 21CFR Part 11 Compliance - Product Thumbnail Image

Computer System Auditing 21CFR Part 11 Compliance

  • Training
  • 60 Minutes
  • Global
Federal Corrupt Practices Act - How Your Institution Can Comply - Product Thumbnail Image

Federal Corrupt Practices Act - How Your Institution Can Comply

  • Training
  • 60 Minutes
  • Global
Why investigators often lose money in conducting sponsored clinical trials - Product Thumbnail Image

Why investigators often lose money in conducting sponsored clinical trials

  • Training
  • 60 Minutes
  • Global
Conflict resolution: A win/win proposition and strategy - Product Thumbnail Image

Conflict resolution: A win/win proposition and strategy

  • Training
  • 60 Minutes
  • Global
Project Manage Your Validation Project -- Introduction to Initiating and Planning a Validation Project - Part 1 - Product Thumbnail Image

Project Manage Your Validation Project -- Introduction to Initiating and Planning a Validation Project - Part 1

  • Training
  • 60 Minutes
  • Global
Domestic C-TPAT Validation Visit Preparation - Product Thumbnail Image

Domestic C-TPAT Validation Visit Preparation

  • Training
  • 60 Minutes
  • Global
Loading Indicator