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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.

Handling Payroll Overpayments - Webinar (Recorded) - Product Thumbnail Image

Handling Payroll Overpayments - Webinar (Recorded)

  • Webinar
  • July 2022
  • 60 Minutes
  • Global
How to Construct an HR Center of Excellence - Webinar (Recorded) - Product Thumbnail Image

How to Construct an HR Center of Excellence - Webinar (Recorded)

  • Webinar
  • July 2022
  • 60 Minutes
  • Global
California GIG Worker Protections: Regulating the Relationships between Organizations & Their GIG Workers - Webinar (Recorded) - Product Thumbnail Image

California GIG Worker Protections: Regulating the Relationships between Organizations & Their GIG Workers - Webinar (Recorded)

  • Webinar
  • July 2022
  • 60 Minutes
  • United States
Cybersecurity and US FDA Requirements - Webinar - Webinar (Recorded) - Product Thumbnail Image

Cybersecurity and US FDA Requirements - Webinar - Webinar (Recorded)

  • Webinar
  • November 2022
  • 90 Minutes
  • United States
Human Factors/Usability Studies following ISO 62366 and the new FDA Guidance - Webinar (Recorded) - Product Thumbnail Image

Human Factors/Usability Studies following ISO 62366 and the new FDA Guidance - Webinar (Recorded)

  • Webinar
  • November 2022
  • 60 Minutes
  • Global
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
Increased Tariffs and Sanctions against China: How to Mitigate Your Exposure and be Compliant - Webinar (Recorded) - Product Thumbnail Image

Increased Tariffs and Sanctions against China: How to Mitigate Your Exposure and be Compliant - Webinar (Recorded)

  • Webinar
  • April 2023
  • 60 Minutes
  • China
Lead Auditor EN ISO 13485:2021 and EU IVDR 2017/746 - Regulation - Webinar (Recorded) - Product Thumbnail Image

Lead Auditor EN ISO 13485:2021 and EU IVDR 2017/746 - Regulation - Webinar (Recorded)

  • Webinar
  • April 2023
  • 90 Minutes
  • Europe
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
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
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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