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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.

Analytical Method Validation, Verification and Transfer (Recorded) - Product Thumbnail Image

Analytical Method Validation, Verification and Transfer (Recorded)

  • Training
  • March 2021
  • 2 Days
  • Global
From
Lifecycle Management of Analytical Methods and Procedures according to new USP and ICH Guidelines (Recorded) - Product Thumbnail Image

Lifecycle Management of Analytical Methods and Procedures according to new USP and ICH Guidelines (Recorded)

  • Training
  • December 2021
  • 2 Days
  • Global
From
Cleanroom, Microbiology and Sterility Assurance Practices for Drug and Device Manufacturers - Product Thumbnail Image

Cleanroom, Microbiology and Sterility Assurance Practices for Drug and Device Manufacturers

  • Training
  • 90 Minutes
  • Global
Verification and Validation - Product, Equipment/Process, Software and QMS (Recorded) - Product Thumbnail Image

Verification and Validation - Product, Equipment/Process, Software and QMS (Recorded)

  • Training
  • January 2022
  • 2 Days
  • Global
From
FinCEN Compliance for MSBs - Tricks to Maintaining Compliance - Product Thumbnail Image

FinCEN Compliance for MSBs - Tricks to Maintaining Compliance

  • Training
  • 60 Minutes
  • Global
Using Controls and Segregation of Duties to Build a Bullet Proof AP Operation - Product Thumbnail Image

Using Controls and Segregation of Duties to Build a Bullet Proof AP Operation

  • Training
  • 60 Minutes
  • Global
Implementing Operations Risk Management within an ERM Framework - Product Thumbnail Image

Implementing Operations Risk Management within an ERM Framework

  • Training
  • 90 Minutes
  • Global
Updates to the EPA Hazardous Waste Pharmaceuticals Rules and Nicotine (P074) Listing - Product Thumbnail Image

Updates to the EPA Hazardous Waste Pharmaceuticals Rules and Nicotine (P074) Listing

  • Training
  • 60 Minutes
  • Global
When and Why to file an Automated Export System (AES) - Product Thumbnail Image

When and Why to file an Automated Export System (AES)

  • Training
  • 60 Minutes
  • Global
How to write SOP's that Avoid Human Error - Product Thumbnail Image

How to write SOP's that Avoid Human Error

  • Training
  • 90 Minutes
  • Global
ANDA Submission and GDUFA Guidance - Product Thumbnail Image

ANDA Submission and GDUFA Guidance

  • Training
  • 60 Minutes
  • Global
Banking MSBs: BSA/AML Risks, Mitigation of Risks and Rewards - Product Thumbnail Image

Banking MSBs: BSA/AML Risks, Mitigation of Risks and Rewards

  • Training
  • 60 Minutes
  • Global
21 CFR Part 11, FDA's Guidance for Electronic Records and Electronic Signatures - Product Thumbnail Image

21 CFR Part 11, FDA's Guidance for Electronic Records and Electronic Signatures

  • Training
  • 90 Minutes
  • Global
The Physician Advisor's Role in Case Management - Product Thumbnail Image

The Physician Advisor's Role in Case Management

  • Training
  • 60 Minutes
  • Global
Breaking the Mold: Best Practices for Mycotoxins Prevention and Control in Food - Product Thumbnail Image

Breaking the Mold: Best Practices for Mycotoxins Prevention and Control in Food

  • Training
  • 60 Minutes
  • Global
Wage & Hour Laws: Ensuring Compliance with the Fair Labor Standards Act in 2022 - Product Thumbnail Image

Wage & Hour Laws: Ensuring Compliance with the Fair Labor Standards Act in 2022

  • Training
  • 75 Minutes
  • Global
Compliance with the American with Disabilities Act (ADA): What Employers Need to Know in 2022 - Product Thumbnail Image

Compliance with the American with Disabilities Act (ADA): What Employers Need to Know in 2022

  • Training
  • 90 Minutes
  • United States
Medical Device Single Audit Program [MDSAP] Implementation & Participating Country Regulatory Processes: U.S., Canada, Brazil, Australia and Japan - Product Thumbnail Image

Medical Device Single Audit Program [MDSAP] Implementation & Participating Country Regulatory Processes: U.S., Canada, Brazil, Australia and Japan

  • Training
  • 90 Minutes
  • Australia, Brazil, ... Australia, Brazil, Canada, Japan, United States
Biostatistics for the Non-Statistician (Recorded) - Product Thumbnail Image

Biostatistics for the Non-Statistician (Recorded)

  • Training
  • December 2021
  • 1 Day
  • Global
From
Sustainable Compliance for Out of Specifications (OOS) Results, Deviations, and Corrective and Preventive Actions (CAPA) (Recorded) - Product Thumbnail Image

Sustainable Compliance for Out of Specifications (OOS) Results, Deviations, and Corrective and Preventive Actions (CAPA) (Recorded)

  • Training
  • November 2021
  • 2 Days
  • Global
From
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