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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.

Quantitative Approach to User Requirements Risk Assessment - Product Thumbnail Image

Quantitative Approach to User Requirements Risk Assessment

  • Training
  • 60 Minutes
  • Global
GSA Schedule Recordkeeping - the 21 Documentation Libraries every Schedule contractor must have - Product Thumbnail Image

GSA Schedule Recordkeeping - the 21 Documentation Libraries every Schedule contractor must have

  • Training
  • 60 Minutes
  • Global
Cleanroom Design, Certification & Classification - Product Thumbnail Image

Cleanroom Design, Certification & Classification

  • Training
  • 60 Minutes
  • Global
Project Manage Your Validation Project -- An Overview - Product Thumbnail Image

Project Manage Your Validation Project -- An Overview

  • Training
  • 60 Minutes
  • Global
An Overview of Design and Development Planning - Product Thumbnail Image

An Overview of Design and Development Planning

  • Training
  • 60 Minutes
  • Global
From CAPA to Capability: Shifting the Focus to Profitability - Product Thumbnail Image

From CAPA to Capability: Shifting the Focus to Profitability

  • Training
  • 60 Minutes
  • Global
CAPA Essentials - core principles and practices needed to implement an effective and efficient CAPA process - Product Thumbnail Image

CAPA Essentials - core principles and practices needed to implement an effective and efficient CAPA process

  • Training
  • 60 Minutes
  • Global
PET Container Stress Cracking - Mythology and Science - Product Thumbnail Image

PET Container Stress Cracking - Mythology and Science

  • Training
  • 60 Minutes
  • Global
Risk Based Validation of Software and Computer Systems - Product Thumbnail Image

Risk Based Validation of Software and Computer Systems

  • Training
  • 60 Minutes
  • Global
Understanding the systems to support compliance with GSA Schedule IFF, TAA and Price Reductions Clause requirements - Product Thumbnail Image

Understanding the systems to support compliance with GSA Schedule IFF, TAA and Price Reductions Clause requirements

  • Training
  • 60 Minutes
  • Global
Introduction to Validation of Measurements (Gauge R&R) - Product Thumbnail Image

Introduction to Validation of Measurements (Gauge R&R)

  • Training
  • 60 Minutes
  • Global
Medical IT Device Security: Why Medical Device Manufacturers Must Take the Lead and Drive Regulatory Compliance - Product Thumbnail Image

Medical IT Device Security: Why Medical Device Manufacturers Must Take the Lead and Drive Regulatory Compliance

  • Training
  • 60 Minutes
  • Global
Bringing FDA Pharmaceutical GMPs into the 21st Century - Product Thumbnail Image

Bringing FDA Pharmaceutical GMPs into the 21st Century

  • Training
  • 60 Minutes
  • Global
An Overview of Risk Management and Risk Analysis Techniques - Product Thumbnail Image

An Overview of Risk Management and Risk Analysis Techniques

  • Training
  • 60 Minutes
  • Global
Internal Auditing Essentials for Medical Device Manufacturers to comply with FDA QSR and ISO13485 - Product Thumbnail Image

Internal Auditing Essentials for Medical Device Manufacturers to comply with FDA QSR and ISO13485

  • Training
  • 60 Minutes
  • Global
Implementing a Comprehensive Vendor Management and Oversight Program - Product Thumbnail Image

Implementing a Comprehensive Vendor Management and Oversight Program

  • Training
  • 60 Minutes
  • Global
The Basics of GSA Schedule Compliance - Product Thumbnail Image

The Basics of GSA Schedule Compliance

  • Training
  • 60 Minutes
  • Global
Effectively application of FMEA as a Risk Management Tool and meet ISO 13485:2003 Risk Management (ISO 14971) Requirements - Product Thumbnail Image

Effectively application of FMEA as a Risk Management Tool and meet ISO 13485:2003 Risk Management (ISO 14971) Requirements

  • Training
  • 60 Minutes
  • Global
The Revision of the Medical Devices Directive 93/42/EEC, Background, Proposal and What It Means - Product Thumbnail Image

The Revision of the Medical Devices Directive 93/42/EEC, Background, Proposal and What It Means

  • Training
  • 60 Minutes
  • Global
Best Practices in Monitoring and Measurement Tools & Techniques to ensure that Your Organization's Processes are performing Up to Expectations - Product Thumbnail Image

Best Practices in Monitoring and Measurement Tools & Techniques to ensure that Your Organization's Processes are performing Up to Expectations

  • Training
  • Global
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