+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 - Market Research Reports

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.

Implementation of the USP GMP Potency Bioassay Suite - Product Thumbnail Image

Implementation of the USP GMP Potency Bioassay Suite

  • Training
  • 60 Minutes
  • Global
Introduction to FDA Good Documentation Practices - Product Thumbnail Image

Introduction to FDA Good Documentation Practices

  • Training
  • 60 Minutes
  • Global
Validation of Bioanalytical Assays for Biologicals - Product Thumbnail Image

Validation of Bioanalytical Assays for Biologicals

  • Training
  • 75 Minutes
  • Global
Food Recalls - Planning and conducting a Food Recall and Crisis Communication - Product Thumbnail Image

Food Recalls - Planning and conducting a Food Recall and Crisis Communication

  • Training
  • 90 Minutes
  • Global
Vendor Qualification Auditing for FDA Computer System Compliance - Product Thumbnail Image

Vendor Qualification Auditing for FDA Computer System Compliance

  • Training
  • 90 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
The multinational scopes of US and EU export controls and economic sanctions laws - Product Thumbnail Image

The multinational scopes of US and EU export controls and economic sanctions laws

  • Training
  • 60 Minutes
  • United States, Europe United States, Europe
Gamma Sterilizer Validation: Method 1 and VDmax25 per ISO 11137 - Product Thumbnail Image

Gamma Sterilizer Validation: Method 1 and VDmax25 per ISO 11137

  • Training
  • 60 Minutes
  • Global
Best Practices for Writing an Effective SOP to Lead to Successful FDA Inspections - Product Thumbnail Image

Best Practices for Writing an Effective SOP to Lead to Successful FDA Inspections

  • Training
  • 60 Minutes
  • Global
Critical Role of Quality Audit in GxP Compliance & Improvement - Product Thumbnail Image

Critical Role of Quality Audit in GxP Compliance & Improvement

  • Training
  • 60 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
Conducting Successful Product Complaint Investigations - Product Thumbnail Image

Conducting Successful Product Complaint Investigations

  • Training
  • 89 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
Environmental Monitoring and the Contamination Control Plan - Product Thumbnail Image

Environmental Monitoring and the Contamination Control Plan

  • Training
  • 95 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
Loading Indicator