+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.

Essentials of Sterilizing Grade Filter Validation - Product Thumbnail Image

Essentials of Sterilizing Grade Filter Validation

  • Training
  • 75 Minutes
  • Global
Gluten-Free Labeling Under the Current Food Allergen Labeling and Consumer Protection Act (FALCPA) of 2004 and Beyond - Product Thumbnail Image

Gluten-Free Labeling Under the Current Food Allergen Labeling and Consumer Protection Act (FALCPA) of 2004 and Beyond

  • Training
  • 60 Minutes
  • Global
Product Complaint Investigations - The application of Lean Six Sigma methodology for U.S. FDA-Regulated Industries - Product Thumbnail Image

Product Complaint Investigations - The application of Lean Six Sigma methodology for U.S. FDA-Regulated Industries

  • Training
  • 75 Minutes
  • United States
Healthcare Data Breach - Have you secured your patient data? - Product Thumbnail Image

Healthcare Data Breach - Have you secured your patient data?

  • Training
  • 60 Minutes
  • Global
Food Recalls - Planning and conducting a Food Recall and Crisis Communication - Product Thumbnail Image

Food Recalls - Planning and conducting a Food Recall and Crisis Communication

  • Training
  • 75 Minutes
  • Global
Computerized System Validation - A Detailed Insight - Product Thumbnail Image

Computerized System Validation - A Detailed Insight

  • Training
  • 90 Minutes
  • Global
The Informed Consent Process at the Investigator Site- Who decides if it is adequate and GCP compliant, Ethics Committee, Sponsor, or Investigator? - Product Thumbnail Image

The Informed Consent Process at the Investigator Site- Who decides if it is adequate and GCP compliant, Ethics Committee, Sponsor, or Investigator?

  • Training
  • 75 Minutes
  • Global
Internal Controls in Purchases, Accounts Payable and Payment - Product Thumbnail Image

Internal Controls in Purchases, Accounts Payable and Payment

  • Training
  • 90 Minutes
  • Global
Personnel Practices and Microbial Control in Pharmaceutical, Biotech, and Medical Device Manufacturing - Product Thumbnail Image

Personnel Practices and Microbial Control in Pharmaceutical, Biotech, and Medical Device Manufacturing

  • Training
  • 90 Minutes
  • Global
HACCP Webinar: Setting up HACCP Plans for Small Companies - Webinar - Product Thumbnail Image

HACCP Webinar: Setting up HACCP Plans for Small Companies - Webinar

  • Webinar
  • 60 Minutes
  • Global
Handling an OSHA Citation - The Process, Your Rights and Opportunities - Product Thumbnail Image

Handling an OSHA Citation - The Process, Your Rights and Opportunities

  • Training
  • 90 Minutes
  • Global
Food Allergen Labeling - Complying with FALCPA and FSMA - Product Thumbnail Image

Food Allergen Labeling - Complying with FALCPA and FSMA

  • Training
  • 60 Minutes
  • Global
SOX Compliance: Accounts Receivable Risks and Controls - Product Thumbnail Image

SOX Compliance: Accounts Receivable Risks and Controls

  • Training
  • 60 Minutes
  • Global
Safety Committees - How they Help with OSHA Compliance and Improve Safety - Product Thumbnail Image

Safety Committees - How they Help with OSHA Compliance and Improve Safety

  • Training
  • 60 Minutes
  • Global
Fundamentals of the Family and Medical Leave Act - Product Thumbnail Image

Fundamentals of the Family and Medical Leave Act

  • Training
  • 60 Minutes
  • Global
OSHA Ergonomics Compliance - What Every Organization Needs to Know - Product Thumbnail Image

OSHA Ergonomics Compliance - What Every Organization Needs to Know

  • Training
  • 60 Minutes
  • Global
Non-inferiority Trials: Practical Issues and Current Regulatory Perspectives - Product Thumbnail Image

Non-inferiority Trials: Practical Issues and Current Regulatory Perspectives

  • Training
  • 60 Minutes
  • Global
Interpreting FDA's New Guidance Document on Risk-based Monitoring - Product Thumbnail Image

Interpreting FDA's New Guidance Document on Risk-based Monitoring

  • Training
  • 60 Minutes
  • Global
Drafting 510(k) Submissions Under New FDA Policies - 2012 & Beyond - Product Thumbnail Image

Drafting 510(k) Submissions Under New FDA Policies - 2012 & Beyond

  • Training
  • 90 Minutes
  • Global
When does GCP Non-compliance at an investigator site compromise a regulatory submission? To File Or Not To File - that is the question! - Product Thumbnail Image

When does GCP Non-compliance at an investigator site compromise a regulatory submission? To File Or Not To File - that is the question!

  • Training
  • 75 Minutes
  • Global
Loading Indicator