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Compliance Online - Market Research Reports

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
Tracking Use Error Risks in Post-Market Surveillance and CAPA Activities - Product Thumbnail Image

Tracking Use Error Risks in Post-Market Surveillance and CAPA Activities

  • Training
  • 60 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
ISO 17025 - The elements of good management system for the competence of testing and calibration in laboratories - Product Thumbnail Image

ISO 17025 - The elements of good management system for the competence of testing and calibration in laboratories

  • 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
Problem Solving Using a Combination of Lean, Six Sigma and ISO 9001:2000 Tools - Product Thumbnail Image

Problem Solving Using a Combination of Lean, Six Sigma and ISO 9001:2000 Tools

  • Training
  • 60 Minutes
  • Global
Root Cause Analysis for Corrective and Preventive Action (CAPA) - Product Thumbnail Image

Root Cause Analysis for Corrective and Preventive Action (CAPA)

  • Training
  • 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
The CAPA Trap or Common Problems and Pitfalls - Product Thumbnail Image

The CAPA Trap or Common Problems and Pitfalls

  • 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
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