+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.

Managing Immunogenicity Risk in Biopharmaceuticals - Product Thumbnail Image

Managing Immunogenicity Risk in Biopharmaceuticals

  • Training
  • 60 Minutes
  • Global
3-hr Virtual Seminar- Medical Device Adverse Event Reporting and Vigilance System During Clinical Trials and Post-Marketing: US, EU, and Canada - Product Thumbnail Image

3-hr Virtual Seminar- Medical Device Adverse Event Reporting and Vigilance System During Clinical Trials and Post-Marketing: US, EU, and Canada

  • Training
  • 3 Hours
  • Canada, United States, ... Canada, United States, Europe
Social Media in a Regulated Environment (for Financial Services) - Product Thumbnail Image

Social Media in a Regulated Environment (for Financial Services)

  • Training
  • 75 Minutes
  • Global
Dissolution Instrument Qualification to Meet Requirements and Minimize Product OOS Dissolution Results - Product Thumbnail Image

Dissolution Instrument Qualification to Meet Requirements and Minimize Product OOS Dissolution Results

  • Training
  • 120 Minutes
  • Global
Understanding Design Controls for Medical Devices - Product Thumbnail Image

Understanding Design Controls for Medical Devices

  • Training
  • 60 Minutes
  • Global
COBIT and ITIL Framework Alignment to Improve the IT Organization while Improving Compliance - Product Thumbnail Image

COBIT and ITIL Framework Alignment to Improve the IT Organization while Improving Compliance

  • Training
  • 120 Minutes
  • Global
Preventing Listeria in RTE processing plants - Product Thumbnail Image

Preventing Listeria in RTE processing plants

  • Training
  • 60 Minutes
  • Global
Clinical Trial auditing - Identifying risks and building a more compliant and successful trial - Product Thumbnail Image

Clinical Trial auditing - Identifying risks and building a more compliant and successful trial

  • Training
  • 90 Minutes
  • Global
The FDA's final Medical Device Data System (MDDS) rule and its implications for currently regulated and unregulated vendors and providers - Product Thumbnail Image

The FDA's final Medical Device Data System (MDDS) rule and its implications for currently regulated and unregulated vendors and providers

  • Training
  • 65 Minutes
  • Global
Understanding the new International and FDA accepted Software Development Standard IEC 62304 - Product Thumbnail Image

Understanding the new International and FDA accepted Software Development Standard IEC 62304

  • Training
  • 60 Minutes
  • Global
How to successfully audit software systems, and thereby avoid having FDA write software-related 483's and warning letters - Product Thumbnail Image

How to successfully audit software systems, and thereby avoid having FDA write software-related 483's and warning letters

  • Training
  • 60 Minutes
  • Global
What will FDA expect and request from your firm during Design Control portions of Inspections? - Product Thumbnail Image

What will FDA expect and request from your firm during Design Control portions of Inspections?

  • Training
  • 60 Minutes
  • Global
What are DHF, DMR and DHR? - The FDA Quality Systems Regulations Records Explained - Product Thumbnail Image

What are DHF, DMR and DHR? - The FDA Quality Systems Regulations Records Explained

  • Training
  • 85 Minutes
  • Global
Record Keeping for a food Recall: Keeping Records to Minimize the Affect of a Recall - Product Thumbnail Image

Record Keeping for a food Recall: Keeping Records to Minimize the Affect of a Recall

  • Training
  • 60 Minutes
  • Global
Selection and Use of (Certified) Reference Material- Strategies for FDA Compliance and Tools for Implementation - Product Thumbnail Image

Selection and Use of (Certified) Reference Material- Strategies for FDA Compliance and Tools for Implementation

  • Training
  • 80 Minutes
  • Global
Understanding the Harmonized Microbial Limits Tests - stressing the new compendial chapters, validation, verification and new expectations in USP <1111> - Product Thumbnail Image

Understanding the Harmonized Microbial Limits Tests - stressing the new compendial chapters, validation, verification and new expectations in USP <1111>

  • Training
  • 85 Minutes
  • Global
EFFECTIVE INVESTIGATIONS What to Do When the Unexpected Happens! - Proper Investigation of Quality Events - Product Thumbnail Image

EFFECTIVE INVESTIGATIONS What to Do When the Unexpected Happens! - Proper Investigation of Quality Events

  • Training
  • 70 Minutes
  • Global
Design Controls Basics - From Design Inputs to Design Outputs and Effective Design Transfer - Product Thumbnail Image

Design Controls Basics - From Design Inputs to Design Outputs and Effective Design Transfer

  • Training
  • 60 Minutes
  • Global
Viral Validation for Biopharmaceuticals - Product Thumbnail Image

Viral Validation for Biopharmaceuticals

  • Training
  • 60 Minutes
  • Global
Quality & Finance: Creating a Balance Using Lean Principles - Product Thumbnail Image

Quality & Finance: Creating a Balance Using Lean Principles

  • Training
  • 60 Minutes
  • Global
Loading Indicator