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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.

Reduce the cost of Sarbanes Oxley Compliance using Control Automation - Product Thumbnail Image

Reduce the cost of Sarbanes Oxley Compliance using Control Automation

  • Training
  • 60 Minutes
  • Global
ISO 9001:2000 1st, 2nd and 3rd Party Auditing & Implementation - Product Thumbnail Image

ISO 9001:2000 1st, 2nd and 3rd Party Auditing & Implementation

  • Training
  • 60 Minutes
  • Global
Develop and execute an Enterprise Risk Management (ERM) system - 6 part course series - Product Thumbnail Image

Develop and execute an Enterprise Risk Management (ERM) system - 6 part course series

  • Training
  • Global
The 510(k) Process: Evaluating Substantial Equivalence in Premarket Notifications - Product Thumbnail Image

The 510(k) Process: Evaluating Substantial Equivalence in Premarket Notifications

  • Training
  • 60 Minutes
  • Global
Biocompatibility Testing: What You Need to Know - Product Thumbnail Image

Biocompatibility Testing: What You Need to Know

  • Training
  • 1 Day
  • Global
From
Terminally Sterilized Pharmaceutical Products - Parametric Release ( New USP<1222>, November 2019) and its Relationship to the new British Terminal Steriliation Methodology (March 2019) (Recorded) - Product Thumbnail Image

Terminally Sterilized Pharmaceutical Products - Parametric Release ( New USP<1222>, November 2019) and its Relationship to the new British Terminal Steriliation Methodology (March 2019) (Recorded)

  • Training
  • August 2024
  • 90 Minutes
  • United Kingdom
EU Medical Device Regulation (MDR) - Updated CE Marking Process and ISO 13485:2016 Expectations - Product Thumbnail Image

EU Medical Device Regulation (MDR) - Updated CE Marking Process and ISO 13485:2016 Expectations

  • Training
  • 90 Minutes
  • Europe
The recent changes in the Brazilian regulatory system - What are the predict for pharmaceutical, medical, cosmetic and food control in the new government? - Product Thumbnail Image

The recent changes in the Brazilian regulatory system - What are the predict for pharmaceutical, medical, cosmetic and food control in the new government?

  • Training
  • 3 Hours
  • Brazil
The Brazilian Reimbursement System - Product Thumbnail Image

The Brazilian Reimbursement System

  • Training
  • 90 Minutes
  • Brazil
Mexico Procedures and Documentation - Product Thumbnail Image

Mexico Procedures and Documentation

  • Training
  • 90 Minutes
  • Mexico
How to Prepare for the New EU Medical Device Regulations - Product Thumbnail Image

How to Prepare for the New EU Medical Device Regulations

  • Training
  • 90 Minutes
  • Europe
The Australian AML/CTF Act - Preparing for an Independent Review - Product Thumbnail Image

The Australian AML/CTF Act - Preparing for an Independent Review

  • Training
  • 90 Minutes
  • Australia
Medical Device Registration - Brazil and Argentina - Product Thumbnail Image

Medical Device Registration - Brazil and Argentina

  • Training
  • 90 Minutes
  • Argentina, Brazil
Label Claims for food, Probiotics and Cosmetic products in Brazilian Regulatory System - Product Thumbnail Image

Label Claims for food, Probiotics and Cosmetic products in Brazilian Regulatory System

  • Training
  • 90 Minutes
  • Brazil
Lead Auditor EN ISO 13485:2016 and EU MDR 2017/745 - Regulation - Product Thumbnail Image

Lead Auditor EN ISO 13485:2016 and EU MDR 2017/745 - Regulation

  • Training
  • 90 Minutes
  • Europe
Overview of Medical Device Regulation in Europe - Product Thumbnail Image

Overview of Medical Device Regulation in Europe

  • Training
  • 90 Minutes
  • Europe
EU ISO 13485:2016 Medical Device Quality Management System - Product Thumbnail Image

EU ISO 13485:2016 Medical Device Quality Management System

  • Training
  • 60 Minutes
  • Europe
Japan: Regulatory Compliance Requirements for Life Science Products - Product Thumbnail Image

Japan: Regulatory Compliance Requirements for Life Science Products

  • Training
  • 90 Minutes
  • Japan
Latin America: Understanding Regulatory Compliance Requirements Across the Life Science Industry (Pharmaceuticals, Biologics, Medical Devices, IVDs) (Recorded) - Product Thumbnail Image

Latin America: Understanding Regulatory Compliance Requirements Across the Life Science Industry (Pharmaceuticals, Biologics, Medical Devices, IVDs) (Recorded)

  • Training
  • October 2021
  • 1 Day
  • Latin America
From
Understanding the Brazilian Regulatory Environment for Medical Devices - Product Thumbnail Image

Understanding the Brazilian Regulatory Environment for Medical Devices

  • Training
  • 60 Minutes
  • Brazil
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