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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.

Risk Evaluation and Mitigation Strategies (REMS) what you need to know in order to comply with FDA's new requirements - Product Thumbnail Image

Risk Evaluation and Mitigation Strategies (REMS) what you need to know in order to comply with FDA's new requirements

  • Training
  • 60 Minutes
  • Global
Cleaning & Cleaning Validation; an Overview - Product Thumbnail Image

Cleaning & Cleaning Validation; an Overview

  • Training
  • 60 Minutes
  • Global
Rules of Practice (FSIS) 9CFR part 500 - Product Thumbnail Image

Rules of Practice (FSIS) 9CFR part 500

  • Training
  • 60 Minutes
  • Global
The Reimbursement Process - Product Thumbnail Image

The Reimbursement Process

  • Training
  • 60 Minutes
  • Global
21 CFR Part 11 compliance under the Obama administration - Product Thumbnail Image

21 CFR Part 11 compliance under the Obama administration

  • Training
  • 60 Minutes
  • Global
Critical Control Points (CCP's). Where are they? Why? When? - Product Thumbnail Image

Critical Control Points (CCP's). Where are they? Why? When?

  • Training
  • 60 Minutes
  • Global
cGMP 'Pitfalls' in the QC Laboratory-Preparing the QC Laboratory and Staff for an FDA Inspection - Product Thumbnail Image

cGMP 'Pitfalls' in the QC Laboratory-Preparing the QC Laboratory and Staff for an FDA Inspection

  • Training
  • 60 Minutes
  • Global
Analytical Instrument and Equipment Qualification in GXP and EPA Laboratories: USP 1058 and Beyond - Product Thumbnail Image

Analytical Instrument and Equipment Qualification in GXP and EPA Laboratories: USP 1058 and Beyond

  • Training
  • 90 Minutes
  • Global
Surprise FDA GMP inspection - how to prepare for it - Product Thumbnail Image

Surprise FDA GMP inspection - how to prepare for it

  • Training
  • 90 Minutes
  • Global
Validation & Verification: Differences between USDA and Codex - Product Thumbnail Image

Validation & Verification: Differences between USDA and Codex

  • Training
  • 90 Minutes
  • Global
Using ICH Q9 and Recent FDA Comments as the Foundation for the Planning, Development and Execution of Risk-Based Cleaning Validation Studies - Product Thumbnail Image

Using ICH Q9 and Recent FDA Comments as the Foundation for the Planning, Development and Execution of Risk-Based Cleaning Validation Studies

  • Training
  • 90 Minutes
  • Global
Residual Solvent Analysis According to USP <467> - Understanding and implementing the new USP chapter - Product Thumbnail Image

Residual Solvent Analysis According to USP <467> - Understanding and implementing the new USP chapter

  • Training
  • 60 Minutes
  • Global
Setting up a Quality Management System (QMS) - Product Thumbnail Image

Setting up a Quality Management System (QMS)

  • Training
  • 60 Minutes
  • Global
Design History Files and Technical Files under US FDA and EU MDD - Product Thumbnail Image

Design History Files and Technical Files under US FDA and EU MDD

  • Training
  • 60 Minutes
  • United States, Europe United States, Europe
Practical Process Validations - Pack of Two Courses - Product Thumbnail Image

Practical Process Validations - Pack of Two Courses

  • Training
  • 90 Minutes
  • Global
Practical Process Validation Part 2 - Qualification Steps, Process Controls and Sustainability Strategies - Product Thumbnail Image

Practical Process Validation Part 2 - Qualification Steps, Process Controls and Sustainability Strategies

  • Training
  • Global
International Financial Reporting Standards: The Basics - Product Thumbnail Image

International Financial Reporting Standards: The Basics

  • Training
  • 60 Minutes
  • Global
Practical Process Validation Part 1 - Validation Planning, Prerequisites and Best Practices - Product Thumbnail Image

Practical Process Validation Part 1 - Validation Planning, Prerequisites and Best Practices

  • Training
  • 90 Minutes
  • Global
Clearing up Roles and Responsibilities in the GLPs - Product Thumbnail Image

Clearing up Roles and Responsibilities in the GLPs

  • Training
  • 60 Minutes
  • Global
Contamination Control 101 in Pharmaceutical, Biotech, and Medical Device Clean rooms - Product Thumbnail Image

Contamination Control 101 in Pharmaceutical, Biotech, and Medical Device Clean rooms

  • Training
  • 90 Minutes
  • Global
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