+353-1-416-8900REST OF WORLD
+44-20-3973-8888REST OF WORLD
1-917-300-0470EAST COAST U.S
1-800-526-8630U.S. (TOLL FREE)

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.

CAPA Management and Compliance with Regulatory Requirements - Product Thumbnail Image

CAPA Management and Compliance with Regulatory Requirements

  • Training
  • 75 Minutes
  • Global
Effective CAPA Management: How to Implement a Risk-based Approach to Improve Your Quality System - Product Thumbnail Image

Effective CAPA Management: How to Implement a Risk-based Approach to Improve Your Quality System

  • Training
  • 60 Minutes
  • Global
Designing an Effective Cleaning and Disinfection Program for Pharmaceutical, Biotech, and Medical Device Cleanrooms - Product Thumbnail Image

Designing an Effective Cleaning and Disinfection Program for Pharmaceutical, Biotech, and Medical Device Cleanrooms

  • Training
  • 90 Minutes
  • Global
Investigator responsibility/Legal commitment in drug and device clinical research: the reality - Product Thumbnail Image

Investigator responsibility/Legal commitment in drug and device clinical research: the reality

  • Training
  • 90 Minutes
  • Global
IDE (Investigational Device Exemption) for PMA and 510(k) for CDRH and CBER - Product Thumbnail Image

IDE (Investigational Device Exemption) for PMA and 510(k) for CDRH and CBER

  • Training
  • 60 Minutes
  • Global
Introduction to Process Capability (Cp, CpK, Pp, Ppk) - Product Thumbnail Image

Introduction to Process Capability (Cp, CpK, Pp, Ppk)

  • Training
  • 60 Minutes
  • Global
Learning from Laboratory-related FDA Warning Letters - Product Thumbnail Image

Learning from Laboratory-related FDA Warning Letters

  • Training
  • 90 Minutes
  • Global
Organization of Clinical Datasets in eCTD Submissions - Product Thumbnail Image

Organization of Clinical Datasets in eCTD Submissions

  • Training
  • 90 Minutes
  • Global
Designing an Effective and Efficient Internal Audit Process for Your Quality Management System - Product Thumbnail Image

Designing an Effective and Efficient Internal Audit Process for Your Quality Management System

  • Training
  • 60 Minutes
  • Global
Validating spreadsheets: strategies for satisfying FDA requirements - Product Thumbnail Image

Validating spreadsheets: strategies for satisfying FDA requirements

  • Training
  • 90 Minutes
  • Global
Premarket Approval (PMA) agreement with FDA for the medical device companies - the Requirements - Product Thumbnail Image

Premarket Approval (PMA) agreement with FDA for the medical device companies - the Requirements

  • Training
  • 60 Minutes
  • Global
How to Prepare and Submit a Bullet Proof 510(k) Submission - Product Thumbnail Image

How to Prepare and Submit a Bullet Proof 510(k) Submission

  • Training
  • 60 Minutes
  • Global
Security Standards ISO 27001 and 27002: What they are and how to use them - Product Thumbnail Image

Security Standards ISO 27001 and 27002: What they are and how to use them

  • Training
  • 60 Minutes
  • Global
Small GMP problems which cause the biggest enforcement headaches: how to tackle them - Product Thumbnail Image

Small GMP problems which cause the biggest enforcement headaches: how to tackle them

  • Training
  • 75 Minutes
  • Global
The Employment Law System and how to stay above the legal line - Product Thumbnail Image

The Employment Law System and how to stay above the legal line

  • Training
  • 60 Minutes
  • Global
Data and Safety Monitoring in Clinical Research Involving Human Subjects - When and How - Product Thumbnail Image

Data and Safety Monitoring in Clinical Research Involving Human Subjects - When and How

  • Training
  • 90 Minutes
  • Global
The Essentials of Food and Drug Administration Medical Device Regulations:A Primer for Manufacturers and Suppliers - Registration, Medical Device Reporting, Corrections and Removals (Recalls) - Product Thumbnail Image

The Essentials of Food and Drug Administration Medical Device Regulations:A Primer for Manufacturers and Suppliers - Registration, Medical Device Reporting, Corrections and Removals (Recalls)

  • Training
  • 90 Minutes
  • Global
Conducting Process Audits within both ISO 9001 and ISO 13485 - Product Thumbnail Image

Conducting Process Audits within both ISO 9001 and ISO 13485

  • Training
  • 90 Minutes
  • Global
Validation Requirements Based on ICH Q9 - Product Thumbnail Image

Validation Requirements Based on ICH Q9

  • Training
  • 90 Minutes
  • Global
Process Validation, planning, strategy, requirements, risk assessment, design description - Product Thumbnail Image

Process Validation, planning, strategy, requirements, risk assessment, design description

  • Training
  • 60 Minutes
  • Global
Loading Indicator