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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.

Quality Expectations for Product Development CMC Activities: R & D, GLP or GMP - Product Thumbnail Image

Quality Expectations for Product Development CMC Activities: R & D, GLP or GMP

  • Training
  • 75 Minutes
  • Global
Implementing a Risk-Based Internal CGMP Annual Audit Program - Product Thumbnail Image

Implementing a Risk-Based Internal CGMP Annual Audit Program

  • Training
  • 90 Minutes
  • Global
Managing the IDE (Investigational Device Exemption) Submission for Compliance Success - Product Thumbnail Image

Managing the IDE (Investigational Device Exemption) Submission for Compliance Success

  • Training
  • 90 Minutes
  • Global
Pharmacovigilance aspects of licensing agreements - Product Thumbnail Image

Pharmacovigilance aspects of licensing agreements

  • Training
  • 60 Minutes
  • Global
Process Mapping: A tool to generate process improvements - Product Thumbnail Image

Process Mapping: A tool to generate process improvements

  • Training
  • 60 Minutes
  • Global
Implementing a GCP Vendor Qualification Program: Ensuring your vendors are in compliance with FDA requirements - Product Thumbnail Image

Implementing a GCP Vendor Qualification Program: Ensuring your vendors are in compliance with FDA requirements

  • Training
  • 75 Minutes
  • Global
Pharmaceutical Cleaning Validation - Product Thumbnail Image

Pharmaceutical Cleaning Validation

  • Training
  • 60 Minutes
  • Global
Differences in GMP Requirements between Drugs and Biologicals - Product Thumbnail Image

Differences in GMP Requirements between Drugs and Biologicals

  • Training
  • 60 Minutes
  • Global
Quality by Design: what the FDA wants, what you must do, how you can deliver to their expectations and what relief you can expect - Product Thumbnail Image

Quality by Design: what the FDA wants, what you must do, how you can deliver to their expectations and what relief you can expect

  • Training
  • 60 Minutes
  • Global
The Essentials of Food and Drug Administration Medical Device Regulations: A Primer for Manufacturers and Suppliers - Quality System Regulation - Product Thumbnail Image

The Essentials of Food and Drug Administration Medical Device Regulations: A Primer for Manufacturers and Suppliers - Quality System Regulation

  • Training
  • 90 Minutes
  • Global
Webseminar on Internal Controls for SOX : Pack of Two courses - Product Thumbnail Image

Webseminar on Internal Controls for SOX : Pack of Two courses

  • Training
  • Global
Medical Device Software Risk Analysis - Product Thumbnail Image

Medical Device Software Risk Analysis

  • Training
  • 60 Minutes
  • Global
Risk-Based Software V&V - FDA,GAMP®, 14971 - Product Thumbnail Image

Risk-Based Software V&V - FDA,GAMP®, 14971

  • Training
  • 90 Minutes
  • Global
Develop, Execute and Enforce an Effective Validation Master Plan - Product Thumbnail Image

Develop, Execute and Enforce an Effective Validation Master Plan

  • Training
  • 60 Minutes
  • Global
How to prepare for the unannounced FDA compliance inspection - Product Thumbnail Image

How to prepare for the unannounced FDA compliance inspection

  • Training
  • 60 Minutes
  • Global
Monoclonal Antibodies and Therapeutic Proteins: Designing GLP Compliant Nonclinical Programs to Meet FDA Expectations - Product Thumbnail Image

Monoclonal Antibodies and Therapeutic Proteins: Designing GLP Compliant Nonclinical Programs to Meet FDA Expectations

  • Training
  • 60 Minutes
  • Global
Implementing Process Controls for Optimum Performance of Cell-Based Assays - Product Thumbnail Image

Implementing Process Controls for Optimum Performance of Cell-Based Assays

  • Training
  • 60 Minutes
  • Global
Analytical Instrument Qualification-Understanding the New USP draft Chapter - Product Thumbnail Image

Analytical Instrument Qualification-Understanding the New USP draft Chapter

  • Training
  • 90 Minutes
  • Global
Lean Documents and Document Control - Product Thumbnail Image

Lean Documents and Document Control

  • Training
  • 90 Minutes
  • Global
Hazard Analysis & Risk Management - New 14971 - Product Thumbnail Image

Hazard Analysis & Risk Management - New 14971

  • Training
  • 90 Minutes
  • Global
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