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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.

Contamination Control 101 in Pharmaceutical, Biotech, and Medical Device Clean rooms - Product Thumbnail Image

Contamination Control 101 in Pharmaceutical, Biotech, and Medical Device Clean rooms

  • Training
  • 90 Minutes
  • Global
Investigating Out of Specification Guidance (OOS) in the Laboratory - Product Thumbnail Image

Investigating Out of Specification Guidance (OOS) in the Laboratory

  • Training
  • 60 Minutes
  • Global
Deviations and Process Failures within a CAPA program - Product Thumbnail Image

Deviations and Process Failures within a CAPA program

  • Training
  • 60 Minutes
  • Global
Gage R & R - Improving the Reliability and Reducing the Variation of Your Measurement System - Product Thumbnail Image

Gage R & R - Improving the Reliability and Reducing the Variation of Your Measurement System

  • Training
  • 60 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
Clinical Trials Process: Study Sponsor's and Investigator's Responsibilities - Product Thumbnail Image

Clinical Trials Process: Study Sponsor's and Investigator's Responsibilities

  • Training
  • 60 Minutes
  • Global
Changes to the Medical Devices Directive: 93/42/EEC - Product Thumbnail Image

Changes to the Medical Devices Directive: 93/42/EEC

  • Training
  • 60 Minutes
  • Global
Best Practices in GLP Final Reporting and Study Closure - Product Thumbnail Image

Best Practices in GLP Final Reporting and Study Closure

  • Training
  • 60 Minutes
  • Global
The IDE (Investigational Device Exemption) - It's Purpose and Preparation - Product Thumbnail Image

The IDE (Investigational Device Exemption) - It's Purpose and Preparation

  • Training
  • 60 Minutes
  • Global
Test Method Validation Basics - Ensuring Adequacy and Reliability of Your Test Methods - Product Thumbnail Image

Test Method Validation Basics - Ensuring Adequacy and Reliability of Your Test Methods

  • Training
  • 60 Minutes
  • Global
Internal Control: Concepts & Application - Product Thumbnail Image

Internal Control: Concepts & Application

  • Training
  • 90 Minutes
  • Global
The Food And Drug Amendments Act of 2007-Does IT Affect You? - Product Thumbnail Image

The Food And Drug Amendments Act of 2007-Does IT Affect You?

  • Training
  • 60 Minutes
  • Global
Basics of Writing Validation Protocols for Medical Devices - Product Thumbnail Image

Basics of Writing Validation Protocols for Medical Devices

  • Training
  • 60 Minutes
  • Global
Basic USDA and FDA Food Labeling: Learn to Create Labels in Compliance with Regulations and Understand the Essential Elements of Labels - Product Thumbnail Image

Basic USDA and FDA Food Labeling: Learn to Create Labels in Compliance with Regulations and Understand the Essential Elements of Labels

  • Training
  • 60 Minutes
  • Global
GxP Computer Systems Validation: The Investigator's Point of View - Product Thumbnail Image

GxP Computer Systems Validation: The Investigator's Point of View

  • Training
  • Global
FDA at the Door: Ten Essential Steps for Inspection Success - Product Thumbnail Image

FDA at the Door: Ten Essential Steps for Inspection Success

  • Training
  • 60 Minutes
  • Global
GMP Expectations for Products Used in Early Phase IND Studies - Product Thumbnail Image

GMP Expectations for Products Used in Early Phase IND Studies

  • Training
  • 75 Minutes
  • Global
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