+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.

Good Practices for Data Integrity, the new Guidance and one FDA Inspector's Experience - Product Thumbnail Image

Good Practices for Data Integrity, the new Guidance and one FDA Inspector's Experience

  • Training
  • 60 Minutes
  • Global
Best Practices of Writing SOPs - Product Thumbnail Image

Best Practices of Writing SOPs

  • Training
  • 90 Minutes
  • Global
CGMP controlled Raw Materials - Product Thumbnail Image

CGMP controlled Raw Materials

  • Training
  • 90 Minutes
  • Global
Care of the LGBT Patient and Their Families: Policies, Procedures & Practices to Ensure Quality Care and Reduce Liability - Product Thumbnail Image

Care of the LGBT Patient and Their Families: Policies, Procedures & Practices to Ensure Quality Care and Reduce Liability

  • Training
  • 75 Minutes
  • Global
Design History Files and Technical Files/Design Dossiers - Meeting U.S. FDA CGMPS and the EU's MDD Requirements - Product Thumbnail Image

Design History Files and Technical Files/Design Dossiers - Meeting U.S. FDA CGMPS and the EU's MDD Requirements

  • Training
  • 90 Minutes
  • United States, Europe United States, Europe
Validation Master Plan - The Unwritten Requirements - Product Thumbnail Image

Validation Master Plan - The Unwritten Requirements

  • Training
  • 60 Minutes
  • Global
Effective (FDA Accepted) Responses to FDA-483's and Warning Letters - Product Thumbnail Image

Effective (FDA Accepted) Responses to FDA-483's and Warning Letters

  • Training
  • 60 Minutes
  • Global
How to Write Effective 483 and Warning Letter Responses - Product Thumbnail Image

How to Write Effective 483 and Warning Letter Responses

  • Training
  • 90 Minutes
  • Global
Transfer of Analytical Methods according to USP <1224> - Product Thumbnail Image

Transfer of Analytical Methods according to USP <1224>

  • Training
  • 60 Minutes
  • Global
How to Prepare for an FDA Inspection? - Product Thumbnail Image

How to Prepare for an FDA Inspection?

  • Training
  • 90 Minutes
  • Global
Good Laboratory Practices (GLPs) - Comparing and Contrasting with Good Manufacturing Practices (GMPs) - Product Thumbnail Image

Good Laboratory Practices (GLPs) - Comparing and Contrasting with Good Manufacturing Practices (GMPs)

  • Training
  • 120 Minutes
  • Global
Good Documentation Guideline (Chapter <1029> USP) - Product Thumbnail Image

Good Documentation Guideline (Chapter <1029> USP)

  • Training
  • 60 Minutes
  • Global
How to Ensure Your Foreign Vendors are FDA Compliant: Conducting Vendor Audits, Monitoring, and Using Checklists - Product Thumbnail Image

How to Ensure Your Foreign Vendors are FDA Compliant: Conducting Vendor Audits, Monitoring, and Using Checklists

  • Training
  • 90 Minutes
  • Global
Supplier Quality Assurance Agreements: Why a General Supply Agreement May Not Be Enough with Some Suppliers - Webinar (Recorded) - Product Thumbnail Image

Supplier Quality Assurance Agreements: Why a General Supply Agreement May Not Be Enough with Some Suppliers - Webinar (Recorded)

  • Webinar
  • May 2019
  • 90 Minutes
  • Global
Contracted Services: Ensuring Compliance with the CMS Hospital CoP Standards, Joint Commission and DNV - Product Thumbnail Image

Contracted Services: Ensuring Compliance with the CMS Hospital CoP Standards, Joint Commission and DNV

  • Training
  • 120 Minutes
  • Global
Laboratory Inspection Readiness - Implementing GMPs for the Pharmaceutical Laboratory - Product Thumbnail Image

Laboratory Inspection Readiness - Implementing GMPs for the Pharmaceutical Laboratory

  • Training
  • 90 Minutes
  • Global
The Disruptive Practitioner: A Danger to the Hospital's Operation - Product Thumbnail Image

The Disruptive Practitioner: A Danger to the Hospital's Operation

  • Training
  • 60 Minutes
  • Global
How To Implement An Effective Human Error Reduction Program - Product Thumbnail Image

How To Implement An Effective Human Error Reduction Program

  • Training
  • 90 Minutes
  • Global
Best Practices in Preparation for an FDA Computer System Audit - Product Thumbnail Image

Best Practices in Preparation for an FDA Computer System Audit

  • Training
  • 90 Minutes
  • Global
Data Integrity Compliance for Computer Systems Regulated by FDA - Product Thumbnail Image

Data Integrity Compliance for Computer Systems Regulated by FDA

  • Training
  • 90 Minutes
  • Global
Loading Indicator