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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.

New Medical Device Vigilance Guidelines - Product Thumbnail Image

New Medical Device Vigilance Guidelines

  • Training
  • 60 Minutes
  • Global
How to Prepare for, Manage, and Follow-up to an FDA Inspection - Product Thumbnail Image

How to Prepare for, Manage, and Follow-up to an FDA Inspection

  • Training
  • 60 Minutes
  • Global
Maintaining a Sustainable and Compliant Design Validation System and Using FMEA for Device Manufacturers - Product Thumbnail Image

Maintaining a Sustainable and Compliant Design Validation System and Using FMEA for Device Manufacturers

  • Training
  • 60 Minutes
  • Global
Auditing and Compliance of Biopharmaceutical API Facilities - Product Thumbnail Image

Auditing and Compliance of Biopharmaceutical API Facilities

  • Training
  • 90 Minutes
  • Global
Risk Management as applied to Design Control - Product Thumbnail Image

Risk Management as applied to Design Control

  • Training
  • 60 Minutes
  • Global
Violation...Deviation: Whatever you call them, you need a process to manage them - Product Thumbnail Image

Violation...Deviation: Whatever you call them, you need a process to manage them

  • Training
  • 60 Minutes
  • Global
Investigations of Microbial Data Deviations - Product Thumbnail Image

Investigations of Microbial Data Deviations

  • Training
  • 90 Minutes
  • Global
What are best practices for creating a Risk Management File? - Product Thumbnail Image

What are best practices for creating a Risk Management File?

  • Training
  • 60 Minutes
  • Global
Preparing for Regulatory Audits - Product Thumbnail Image

Preparing for Regulatory Audits

  • Training
  • 60 Minutes
  • Global
Combination products and convergence: an overview of clinical benefits, regulatory issues and manufacturing challenges - part 2 - Product Thumbnail Image

Combination products and convergence: an overview of clinical benefits, regulatory issues and manufacturing challenges - part 2

  • Training
  • 90 Minutes
  • Global
How to perform effective supplier audits, and avoid FDA 483 - Product Thumbnail Image

How to perform effective supplier audits, and avoid FDA 483

  • Training
  • 60 Minutes
  • Global
Food Labeling 101: A Basic Guide for Manufacturers, Importers, and Label Designers - Product Thumbnail Image

Food Labeling 101: A Basic Guide for Manufacturers, Importers, and Label Designers

  • Training
  • 60 Minutes
  • Global
Validation of Rapid Microbiological Methods - Product Thumbnail Image

Validation of Rapid Microbiological Methods

  • Training
  • 90 Minutes
  • Global
Meeting FDA Requirements for Over-the-Counter / OTC Drug Labeling - Product Thumbnail Image

Meeting FDA Requirements for Over-the-Counter / OTC Drug Labeling

  • Training
  • 60 Minutes
  • Global
Qualification and Audit of Suppliers and Vendors - A Risk Based Approach - Product Thumbnail Image

Qualification and Audit of Suppliers and Vendors - A Risk Based Approach

  • Training
  • 90 Minutes
  • Global
Bringing Compliance to Design Control through Life Cycle Management of Older Medical Devices and Surgical Instruments - Product Thumbnail Image

Bringing Compliance to Design Control through Life Cycle Management of Older Medical Devices and Surgical Instruments

  • Training
  • 60 Minutes
  • Global
Aerospace -Transitioning to AS9100 Rev.C - Product Thumbnail Image

Aerospace -Transitioning to AS9100 Rev.C

  • Training
  • 60 Minutes
  • Global
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
Software Verification and Validation For FDA-Regulated Industries - Product Thumbnail Image

Software Verification and Validation For FDA-Regulated Industries

  • 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
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