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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.

Japan - Regulatory Filing Requirements and Compliance Processes for Life Sciences PART I - Product Thumbnail Image

Japan - Regulatory Filing Requirements and Compliance Processes for Life Sciences PART I

  • Training
  • 90 Minutes
  • Japan
Japanese PAL - Navigating the Japanese Pharmaceutical Affairs Law - Product Thumbnail Image

Japanese PAL - Navigating the Japanese Pharmaceutical Affairs Law

  • Training
  • 90 Minutes
  • Japan
The EU Clinical Trial Directive - Product Thumbnail Image

The EU Clinical Trial Directive

  • Training
  • 90 Minutes
  • Europe
Understanding the Pharmaceutical Supply Chain in China Risks, Rewards, Solutions - Product Thumbnail Image

Understanding the Pharmaceutical Supply Chain in China Risks, Rewards, Solutions

  • Training
  • 60 Minutes
  • China
Japan PAL Audits performed abroad by the PMDA: What to expect and how to prepare - Product Thumbnail Image

Japan PAL Audits performed abroad by the PMDA: What to expect and how to prepare

  • Training
  • 90 Minutes
  • Japan
4-Region internal audits: Medical Device Quality System audits that cover internal regulatory compliance for FDA, Europe, Canada and Japan - Product Thumbnail Image

4-Region internal audits: Medical Device Quality System audits that cover internal regulatory compliance for FDA, Europe, Canada and Japan

  • Training
  • 60 Minutes
  • Canada, Japan, Europe Canada, Japan, Europe
GCP Audit of Clinical Evaluations for Japan: Requirements and expectations from the revised Japanese PAL - Product Thumbnail Image

GCP Audit of Clinical Evaluations for Japan: Requirements and expectations from the revised Japanese PAL

  • Training
  • 60 Minutes
  • Japan
Exporting to Mexico Webinar Series 4: Harmonized System Code Basics and Special Certificates - Webinar - Product Thumbnail Image

Exporting to Mexico Webinar Series 4: Harmonized System Code Basics and Special Certificates - Webinar

  • Webinar
  • 90 Minutes
  • Mexico
Exporting to Mexico Webinar Series 3: INCOTERMS Review and INCOTERM Common Practices in Mexico - Webinar - Product Thumbnail Image

Exporting to Mexico Webinar Series 3: INCOTERMS Review and INCOTERM Common Practices in Mexico - Webinar

  • Webinar
  • 60 Minutes
  • Mexico
Exporting to Mexico Webinar Series 2: How to Settle Disputes with Mexican Customs - Webinar - Product Thumbnail Image

Exporting to Mexico Webinar Series 2: How to Settle Disputes with Mexican Customs - Webinar

  • Webinar
  • 60 Minutes
  • Mexico
Exporting to Mexico Webinar Series 1: Mexican Import Process - Webinar - Product Thumbnail Image

Exporting to Mexico Webinar Series 1: Mexican Import Process - Webinar

  • Webinar
  • 60 Minutes
  • Mexico
Exporting to Mexico Webinar Series: Import Process, Custom Disputes, INCOTERMS & Harmonized System Code - Webinar - Product Thumbnail Image

Exporting to Mexico Webinar Series: Import Process, Custom Disputes, INCOTERMS & Harmonized System Code - Webinar

  • Webinar
  • 4 Hours
  • Mexico
Foreign Corrupt Practices Act & UK Anti-Bribery - Product Thumbnail Image

Foreign Corrupt Practices Act & UK Anti-Bribery

  • Training
  • 60 Minutes
  • United Kingdom
Asian Medical Device Laws and Regulations: China, Hong Kong, Japan and Korea - Product Thumbnail Image

Asian Medical Device Laws and Regulations: China, Hong Kong, Japan and Korea

  • Training
  • 90 Minutes
  • China, Hong Kong, ... China, Hong Kong, Japan, South Korea
Changes to Good Pharmacovigilance Practices in the EU - Product Thumbnail Image

Changes to Good Pharmacovigilance Practices in the EU

  • Training
  • 90 Minutes
  • Europe
Validation of Existing/ Legacy Computer Systems for FDA/EU Compliance - Product Thumbnail Image

Validation of Existing/ Legacy Computer Systems for FDA/EU Compliance

  • Training
  • 75 Minutes
  • Europe
Parallel Scientific Advice: How effective is the system established between the EMEA and the FDA - Product Thumbnail Image

Parallel Scientific Advice: How effective is the system established between the EMEA and the FDA

  • Training
  • 60 Minutes
  • Middle East, Africa, Europe Middle East, Africa, Europe
Update of Pharmaceutical law in the EU -Focus on Generic Opportunities & Biosimilars - Product Thumbnail Image

Update of Pharmaceutical law in the EU -Focus on Generic Opportunities & Biosimilars

  • Training
  • 60 Minutes
  • Europe
Japanese PAL - JPAL Technical, cultural and language challenges when dealing with MAH, PMDA, Distributors and Customers - Product Thumbnail Image

Japanese PAL - JPAL Technical, cultural and language challenges when dealing with MAH, PMDA, Distributors and Customers

  • Training
  • 90 Minutes
  • Japan
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
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