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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.

Delivering Biopharmaceutical Facilities in a Risk Based World: The Role of GEP, QbD, and E2500 - Product Thumbnail Image

Delivering Biopharmaceutical Facilities in a Risk Based World: The Role of GEP, QbD, and E2500

  • Training
  • 60 Minutes
  • Global
Combination products and convergence: an overview of clinical benefits, regulatory issues and manufacturing challenges - part 1 - Product Thumbnail Image

Combination products and convergence: an overview of clinical benefits, regulatory issues and manufacturing challenges - part 1

  • Training
  • 90 Minutes
  • Global
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
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
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
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
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 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
A Practical Approach to Microbial Data Deviation Investigations - Product Thumbnail Image

A Practical Approach to Microbial Data Deviation Investigations

  • Training
  • 90 Minutes
  • Global
'Preventive Action' - the often ignored side of CAPA: Use FMEA to build preventive action into your CAPA program - Product Thumbnail Image

'Preventive Action' - the often ignored side of CAPA: Use FMEA to build preventive action into your CAPA program

  • 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
Principal Investigator responsibility in Research Involving Human Subjects: The International Conference on Harmonization (ICH) view - Product Thumbnail Image

Principal Investigator responsibility in Research Involving Human Subjects: The International Conference on Harmonization (ICH) view

  • Training
  • 90 Minutes
  • Global
Integrating Risk Management with the Quality System - Product Thumbnail Image

Integrating Risk Management with the Quality System

  • Training
  • 90 Minutes
  • Global
How to conduct a Clinical Trial in accordance with FDA regulations and how to avoid the common deficiencies observed during FDA clinical audits - Product Thumbnail Image

How to conduct a Clinical Trial in accordance with FDA regulations and how to avoid the common deficiencies observed during FDA clinical audits

  • Training
  • 90 Minutes
  • Global
510(k) Applications made Simple - Product Thumbnail Image

510(k) Applications made Simple

  • Training
  • 60 Minutes
  • Global
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