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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.

Effective Discipline and Lawsuit-Proof Termination: How to Remedy Performance and Conduct Problems While Minimizing Your Legal Risks - Product Thumbnail Image

Effective Discipline and Lawsuit-Proof Termination: How to Remedy Performance and Conduct Problems While Minimizing Your Legal Risks

  • Training
  • 90 Minutes
  • Global
Batch Production Record (BPR) and Device History Record (DHR) Review and Quality Assessment - Product Thumbnail Image

Batch Production Record (BPR) and Device History Record (DHR) Review and Quality Assessment

  • Training
  • 90 Minutes
  • Global
FDA Regulation of Tobacco Products: The Deeming Regulation - Impact on E-Cigarettes - Product Thumbnail Image

FDA Regulation of Tobacco Products: The Deeming Regulation - Impact on E-Cigarettes

  • Training
  • 60 Minutes
  • Global
Developing and Facilitating Effective Compliance Risk Assessments - Product Thumbnail Image

Developing and Facilitating Effective Compliance Risk Assessments

  • Training
  • 75 Minutes
  • Global
ISO 22000 vs GFSI (SQF, BRC, IFS, and FSSC 22000): Meeting key Requirements - Product Thumbnail Image

ISO 22000 vs GFSI (SQF, BRC, IFS, and FSSC 22000): Meeting key Requirements

  • Training
  • 60 Minutes
  • Global
Multistate Handbooks: Multitasking Policies Effectively - Product Thumbnail Image

Multistate Handbooks: Multitasking Policies Effectively

  • Training
  • 60 Minutes
  • Global
2014 Current Best Practices for Public Company Management - Product Thumbnail Image

2014 Current Best Practices for Public Company Management

  • Training
  • 60 Minutes
  • Global
Ensuring Legally-Effective Informed Consent: Basic to Advanced Issues for Investigators and IRBs - Product Thumbnail Image

Ensuring Legally-Effective Informed Consent: Basic to Advanced Issues for Investigators and IRBs

  • Training
  • 90 Minutes
  • Global
Transforming the Cargo Clearance Process - Product Thumbnail Image

Transforming the Cargo Clearance Process

  • Training
  • 60 Minutes
  • Global
Complying with and Applying Regulator's Rules and Guidance as it Relates to Social Media and Personal Electronic Devices (Financial Services) - Product Thumbnail Image

Complying with and Applying Regulator's Rules and Guidance as it Relates to Social Media and Personal Electronic Devices (Financial Services)

  • Training
  • 90 Minutes
  • Global
Changes in US FDA Enforcement - Product Thumbnail Image

Changes in US FDA Enforcement

  • Training
  • 90 Minutes
  • United States
The Use and Mis-use of FMEA in Medical Device Risk Management - Product Thumbnail Image

The Use and Mis-use of FMEA in Medical Device Risk Management

  • Training
  • 60 Minutes
  • Global
Dual and Third-Country Nationals: Ensuring Foreign Licensee Requirements to Prevent Diversion of ITAR-Controlled Defense Articles - Product Thumbnail Image

Dual and Third-Country Nationals: Ensuring Foreign Licensee Requirements to Prevent Diversion of ITAR-Controlled Defense Articles

  • Training
  • 70 Minutes
  • Global
Selecting the Most Appropriate Predicate Device(S) for your 510(k) Application - Product Thumbnail Image

Selecting the Most Appropriate Predicate Device(S) for your 510(k) Application

  • Training
  • 60 Minutes
  • Global
Equipment Requalification: What and When it is Really Required? - Product Thumbnail Image

Equipment Requalification: What and When it is Really Required?

  • Training
  • 60 Minutes
  • Global
Issues - Terminations and Exits - Legal Compliance - Product Thumbnail Image

Issues - Terminations and Exits - Legal Compliance

  • Training
  • 60 Minutes
  • Global
LDT including CDx; CLIA versus FDA's Authority - Product Thumbnail Image

LDT including CDx; CLIA versus FDA's Authority

  • Training
  • 60 Minutes
  • Global
How to respond to GXP (GCP, GLP, GMP, GPV) Inspection and Audit Findings using Correction and Preventative Action (CAPA) - Product Thumbnail Image

How to respond to GXP (GCP, GLP, GMP, GPV) Inspection and Audit Findings using Correction and Preventative Action (CAPA)

  • Training
  • 60 Minutes
  • Global
FDA Premarket Review of New and Modified Tobacco Products - Product Thumbnail Image

FDA Premarket Review of New and Modified Tobacco Products

  • Training
  • 60 Minutes
  • Global
How to file a 510(k) when your device is (or contains) software - Product Thumbnail Image

How to file a 510(k) when your device is (or contains) software

  • Training
  • 75 Minutes
  • Global
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