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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 Guidance for Industry: CGMP for Phase I Investigational Drugs - Product Thumbnail Image

NEW Guidance for Industry: CGMP for Phase I Investigational Drugs

  • Training
  • 90 Minutes
  • Global
Accounts Receivables: How to Ensure Sarbanes-Oxley Compliance - Product Thumbnail Image

Accounts Receivables: How to Ensure Sarbanes-Oxley Compliance

  • Training
  • 60 Minutes
  • Global
How to Prepare for FDA Compliance - Product Thumbnail Image

How to Prepare for FDA Compliance

  • Training
  • 60 Minutes
  • Global
OSHA injury and illness recordkeeping - Product Thumbnail Image

OSHA injury and illness recordkeeping

  • Training
  • 60 Minutes
  • Global
Reading Between the Lines: Dealing with Gaps in GLP Regulations - Product Thumbnail Image

Reading Between the Lines: Dealing with Gaps in GLP Regulations

  • Training
  • 60 Minutes
  • Global
A FDA Audit - What You Need to Know - Product Thumbnail Image

A FDA Audit - What You Need to Know

  • Training
  • 90 Minutes
  • Global
Quality Expectations for Drugs and Biologics during Early Development: Phase 2 - Product Thumbnail Image

Quality Expectations for Drugs and Biologics during Early Development: Phase 2

  • Training
  • 75 Minutes
  • Global
Complying with Sarbanes Oxley (SOX), Section 404 - Product Thumbnail Image

Complying with Sarbanes Oxley (SOX), Section 404

  • Training
  • 90 Minutes
  • Global
How to implement a sustainable Information Security Management System (ISMS) - Product Thumbnail Image

How to implement a sustainable Information Security Management System (ISMS)

  • Training
  • 60 Minutes
  • Global
Validating Disinfectants for Pharmaceutical and Biotech Operations - Product Thumbnail Image

Validating Disinfectants for Pharmaceutical and Biotech Operations

  • Training
  • 90 Minutes
  • Global
What We Can Learn From Warning Letters - Product Thumbnail Image

What We Can Learn From Warning Letters

  • Training
  • 90 Minutes
  • Global
Preparing for a U.S. FDA Audit - Product Thumbnail Image

Preparing for a U.S. FDA Audit

  • Training
  • 60 Minutes
  • United States
Internal Control and Sarbanes-Oxley Section 404 - Product Thumbnail Image

Internal Control and Sarbanes-Oxley Section 404

  • Training
  • 60 Minutes
  • Global
SOX: Internal Controls for Inventory - Product Thumbnail Image

SOX: Internal Controls for Inventory

  • Training
  • 60 Minutes
  • Global
What to Expect During an FDA Inspection, and How to Handle It - Product Thumbnail Image

What to Expect During an FDA Inspection, and How to Handle It

  • Training
  • 60 Minutes
  • Global
CAPA - Root cause and risk management - Product Thumbnail Image

CAPA - Root cause and risk management

  • Training
  • 40 Minutes
  • Global
Getting the Most Out Of Data Mining for Pharmacovigilance and Risk Management - Product Thumbnail Image

Getting the Most Out Of Data Mining for Pharmacovigilance and Risk Management

  • Training
  • 60 Minutes
  • Global
CAPA Management and Compliance with Regulatory Requirements - Product Thumbnail Image

CAPA Management and Compliance with Regulatory Requirements

  • Training
  • 75 Minutes
  • Global
IDE (Investigational Device Exemption) for PMA and 510(k) for CDRH and CBER - Product Thumbnail Image

IDE (Investigational Device Exemption) for PMA and 510(k) for CDRH and CBER

  • Training
  • 60 Minutes
  • Global
Introduction to Process Capability (Cp, CpK, Pp, Ppk) - Product Thumbnail Image

Introduction to Process Capability (Cp, CpK, Pp, Ppk)

  • Training
  • 60 Minutes
  • Global
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