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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.

New Elemental Impurities Tests for Pharmaceutical Products According to the New ICH Q3D and USP 232/233 Guidelines - Product Thumbnail Image

New Elemental Impurities Tests for Pharmaceutical Products According to the New ICH Q3D and USP 232/233 Guidelines

  • Training
  • 90 Minutes
  • Global
Understanding FDA Design Verification and Validation Requirements for Medical Devices - Product Thumbnail Image

Understanding FDA Design Verification and Validation Requirements for Medical Devices

  • Training
  • 75 Minutes
  • Global
Best Practices for Sexual Harassment Internal Investigations - Product Thumbnail Image

Best Practices for Sexual Harassment Internal Investigations

  • Training
  • 60 Minutes
  • Global
Best Practices of Writing SOPs - Product Thumbnail Image

Best Practices of Writing SOPs

  • Training
  • 90 Minutes
  • Global
State of the Art: Recommendations for writing a thorough SOA and build SOA Libraries for your CERs - Product Thumbnail Image

State of the Art: Recommendations for writing a thorough SOA and build SOA Libraries for your CERs

  • Training
  • 90 Minutes
  • Global
Female to Female Hostility @Workplace: All you need to Know - Product Thumbnail Image

Female to Female Hostility @Workplace: All you need to Know

  • Training
  • 60 Minutes
  • Global
TIN Matching to Reduce Your B-Notices and Eliminate Proposed Penalties - Product Thumbnail Image

TIN Matching to Reduce Your B-Notices and Eliminate Proposed Penalties

  • Training
  • 90 Minutes
  • Global
Consents and 42 CFR Part 2 - New Rules for Re-Release of Substance Use Disorder Information - Product Thumbnail Image

Consents and 42 CFR Part 2 - New Rules for Re-Release of Substance Use Disorder Information

  • Training
  • 90 Minutes
  • Global
Performing an Effective, Robust and Compliant Sterility Failure Investigation: How to Avoid Common Mistakes - Product Thumbnail Image

Performing an Effective, Robust and Compliant Sterility Failure Investigation: How to Avoid Common Mistakes

  • Training
  • 90 Minutes
  • Global
Process Capability for Normal and Non-Normal Data (Focus: Process Stability, Capability and Cp, Cpk, Pp, Ppk, Cpm) - Product Thumbnail Image

Process Capability for Normal and Non-Normal Data (Focus: Process Stability, Capability and Cp, Cpk, Pp, Ppk, Cpm)

  • Training
  • 75 Minutes
  • Global
HIPAA Planning for 2020 and Beyond - Protecting Patient Information Privacy and Security - Product Thumbnail Image

HIPAA Planning for 2020 and Beyond - Protecting Patient Information Privacy and Security

  • Training
  • 90 Minutes
  • Global
How Medicare's Market-Based Payment System Is Upending the U.S. Clinical Laboratory Market - Product Thumbnail Image

How Medicare's Market-Based Payment System Is Upending the U.S. Clinical Laboratory Market

  • Training
  • 90 Minutes
  • United States
HIPAA Training for Security Officers - Product Thumbnail Image

HIPAA Training for Security Officers

  • Training
  • 60 Minutes
  • Global
Approaching Unknown Cause Laboratory Investigations Using Lean Tools - Product Thumbnail Image

Approaching Unknown Cause Laboratory Investigations Using Lean Tools

  • Training
  • 60 Minutes
  • Global
The Low-down on ACH and Regulation E - Product Thumbnail Image

The Low-down on ACH and Regulation E

  • Training
  • 90 Minutes
  • Global
Automating Excel: An Introduction to VBA - Product Thumbnail Image

Automating Excel: An Introduction to VBA

  • Training
  • 90 Minutes
  • Global
Writing Validation Master Plans: Best Practices for Authoring a Compliant Document - Product Thumbnail Image

Writing Validation Master Plans: Best Practices for Authoring a Compliant Document

  • Training
  • 90 Minutes
  • Global
FDA Regulation of Human Cells, Tissues and Cellular and Tissue-Based Products (HCT/Ps) - Product Thumbnail Image

FDA Regulation of Human Cells, Tissues and Cellular and Tissue-Based Products (HCT/Ps)

  • Training
  • 90 Minutes
  • Global
Documentation of Medical Necessity - Focus for OIG and other auditors - Product Thumbnail Image

Documentation of Medical Necessity - Focus for OIG and other auditors

  • Training
  • 60 Minutes
  • Global
The HIPAA Audit Program for 2015 - New Focus, New Process - Product Thumbnail Image

The HIPAA Audit Program for 2015 - New Focus, New Process

  • Training
  • 90 Minutes
  • Global
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