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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.

Ethics and Scientific Misconduct in Regulated Studies - Product Thumbnail Image

Ethics and Scientific Misconduct in Regulated Studies

  • Training
  • 60 Minutes
  • Global
HIPAA and EHRs: How to Comply with the New Regulations and What to Ask of your Vendor - Product Thumbnail Image

HIPAA and EHRs: How to Comply with the New Regulations and What to Ask of your Vendor

  • Training
  • 90 Minutes
  • Global
Software validation and 21 CFR Part 11 remediation planning: FDA inspection strategies - Product Thumbnail Image

Software validation and 21 CFR Part 11 remediation planning: FDA inspection strategies

  • Training
  • 60 Minutes
  • Global
Chemical Safety and Chemical Hygiene Plans for the Lab Environment - Product Thumbnail Image

Chemical Safety and Chemical Hygiene Plans for the Lab Environment

  • Training
  • 60 Minutes
  • Global
Developing and Implementing Golden Parachute Agreements - Product Thumbnail Image

Developing and Implementing Golden Parachute Agreements

  • Training
  • 90 Minutes
  • Global
HR Policies for Small Companies/Organizations - Product Thumbnail Image

HR Policies for Small Companies/Organizations

  • Training
  • 90 Minutes
  • Global
Clinical Trial Auditing - Identifying risks and building a more compliant and successful trial - Product Thumbnail Image

Clinical Trial Auditing - Identifying risks and building a more compliant and successful trial

  • Training
  • 90 Minutes
  • Global
Risk Management for Human Resources - Product Thumbnail Image

Risk Management for Human Resources

  • Training
  • 60 Minutes
  • Global
FDA's Regulation of Veterinary Regenerative Medicine: What Industry Needs to Know to Market and Sell a Stem Cell Product for Use in Dogs, Cats, Horses and other Animals - Product Thumbnail Image

FDA's Regulation of Veterinary Regenerative Medicine: What Industry Needs to Know to Market and Sell a Stem Cell Product for Use in Dogs, Cats, Horses and other Animals

  • Training
  • 60 Minutes
  • Global
Trial Master File for Research Sites: Can You Pass FDA Inspection? - Product Thumbnail Image

Trial Master File for Research Sites: Can You Pass FDA Inspection?

  • Training
  • 60 Minutes
  • Global
cGMPs for Medical Devices, Including In Vitro Diagnostic Devices - Product Thumbnail Image

cGMPs for Medical Devices, Including In Vitro Diagnostic Devices

  • Training
  • 90 Minutes
  • Global
Recommendations for Cell Banks used in GXP testing - Product Thumbnail Image

Recommendations for Cell Banks used in GXP testing

  • Training
  • 60 Minutes
  • Global
Issue Detection and Escalation in Clinical Trial Settings - Product Thumbnail Image

Issue Detection and Escalation in Clinical Trial Settings

  • Training
  • 60 Minutes
  • Global
Medical Device: Risk Assessment and Mitigation through FMEA - Product Thumbnail Image

Medical Device: Risk Assessment and Mitigation through FMEA

  • Training
  • 90 Minutes
  • Global
The U.S. FDA's New Global Engagement Initiative - Product Thumbnail Image

The U.S. FDA's New Global Engagement Initiative

  • Training
  • 90 Minutes
  • United States, Global United States, Global
REMS Update: Risk Evaluation and Mitigation Strategies - what do you need to do now? - Product Thumbnail Image

REMS Update: Risk Evaluation and Mitigation Strategies - what do you need to do now?

  • Training
  • 60 Minutes
  • Global
Common Concerns and Penalties Related to the Americans with Disability Amendments Act (ADAA) - Product Thumbnail Image

Common Concerns and Penalties Related to the Americans with Disability Amendments Act (ADAA)

  • Training
  • 90 Minutes
  • Global
Verification and Validation (V&V) of Software in the Medical Devices - Product Thumbnail Image

Verification and Validation (V&V) of Software in the Medical Devices

  • Training
  • 90 Minutes
  • Global
Unsolicited Drug and Device Off-Label Claims Via Social Media and Risk Management - Product Thumbnail Image

Unsolicited Drug and Device Off-Label Claims Via Social Media and Risk Management

  • Training
  • 60 Minutes
  • Global
Device Corrections and Removals - Product Thumbnail Image

Device Corrections and Removals

  • Training
  • 90 Minutes
  • Global
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