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Compliance Trainings - Market Research Reports

Compliance Trainings, a leading consulting and training portal, focuses on providing regulatory and quality training to professionals and organizations from various industries, across the globe. Since our founding in 2012, we have successfully trained professionals from small and large companies. Our prominent reputation has earned us high recognition of companies who consider us to be an integral part of their technical training programs.

Aseptic Processing and Validation Course - FDA Expectations and Industry Best Practices (Recorded) - Product Thumbnail Image

Aseptic Processing and Validation Course - FDA Expectations and Industry Best Practices (Recorded)

  • Training
  • October 2025
  • 2 Days
  • Global
From
Good Manufacturing Practices (GMP) 101 (Recorded) - Product Thumbnail Image

Good Manufacturing Practices (GMP) 101 (Recorded)

  • Training
  • September 2025
  • 2 Days
  • Global
From
OOS and OOT Investigations Course - Best Practices, Key Components and FDA Requirements (Recorded) - Product Thumbnail Image

OOS and OOT Investigations Course - Best Practices, Key Components and FDA Requirements (Recorded)

  • Training
  • September 2025
  • 2 Days
  • Global
From
Supplier And Contract Manufacturer Management Course (Recorded) - Product Thumbnail Image

Supplier And Contract Manufacturer Management Course (Recorded)

  • Training
  • August 2025
  • 2 Days
  • Global
From
FDA Inspections - Top FDA 483 Observations and Prevention Strategies (Recorded) - Product Thumbnail Image

FDA Inspections - Top FDA 483 Observations and Prevention Strategies (Recorded)

  • Training
  • August 2025
  • 2 Days
  • Global
From
The Art of Technology Transfer in Drug Development: Developing and Building a Framework of Success (Recorded) - Product Thumbnail Image

The Art of Technology Transfer in Drug Development: Developing and Building a Framework of Success (Recorded)

  • Training
  • August 2025
  • 60 Minutes
  • Global
From
Real-World Quality Management Systems and Data Integrity Compliance Tactics (Recorded) - Product Thumbnail Image

Real-World Quality Management Systems and Data Integrity Compliance Tactics (Recorded)

  • Training
  • July 2025
  • 90 Minutes
  • Global
From
Dissolution Testing in Pharma - From Development to Regulatory Approval (Recorded) - Product Thumbnail Image

Dissolution Testing in Pharma - From Development to Regulatory Approval (Recorded)

  • Training
  • July 2025
  • 60 Minutes
  • Global
From
GLP Laboratory Compliance Documentation and Recordkeeping (Recorded) - Product Thumbnail Image

GLP Laboratory Compliance Documentation and Recordkeeping (Recorded)

  • Training
  • July 2025
  • 2 Days
  • Global
From
Technical Writing Excellence in the Life Sciences - A Masterclass (Recorded) - Product Thumbnail Image

Technical Writing Excellence in the Life Sciences - A Masterclass (Recorded)

  • Training
  • June 2024
  • 2 Days
  • Global
From
Using Audit Trails to Support Part 11 Data Integrity Compliance (Recorded) - Product Thumbnail Image

Using Audit Trails to Support Part 11 Data Integrity Compliance (Recorded)

  • Training
  • February 2024
  • 90 Minutes
  • Global
From
e-STAR Submission Program for 510(k), PMA, Q-Submissions and DeNovo (Recorded) - Product Thumbnail Image

e-STAR Submission Program for 510(k), PMA, Q-Submissions and DeNovo (Recorded)

  • Training
  • March 2024
  • 90 Minutes
  • Global
From
Preventive Maintenance and Calibrations - Regulatory Expectations and Best Practices (Recorded) - Product Thumbnail Image

Preventive Maintenance and Calibrations - Regulatory Expectations and Best Practices (Recorded)

  • Training
  • February 2024
  • 90 Minutes
  • Global
From
The US FDA QMSR Transition - 21 CFR 820 and ISO 13485 (Recorded) - Product Thumbnail Image

The US FDA QMSR Transition - 21 CFR 820 and ISO 13485 (Recorded)

  • Training
  • February 2024
  • 90 Minutes
  • United States
From
OOS and Setting Specifications for Pharma, Biopharma and Combination Products (Recorded) - Product Thumbnail Image

OOS and Setting Specifications for Pharma, Biopharma and Combination Products (Recorded)

  • Training
  • February 2024
  • 90 Minutes
  • Global
From
3-Hour Virtual Seminar on Risk Based Approach to IT Infrastructure Qualification, Compliance & Control (Recorded) - Product Thumbnail Image

3-Hour Virtual Seminar on Risk Based Approach to IT Infrastructure Qualification, Compliance & Control (Recorded)

  • Training
  • March 2024
  • 3 Hours
  • Global
From
Project Management in the Biomedical Industry (Recorded) - Product Thumbnail Image

Project Management in the Biomedical Industry (Recorded)

  • Training
  • April 2024
  • 90 Minutes
  • Global
From
Role of Project Management in Quality Planning Throughout the Medical Device Project Lifecycle (Recorded) - Product Thumbnail Image

Role of Project Management in Quality Planning Throughout the Medical Device Project Lifecycle (Recorded)

  • Training
  • April 2024
  • 120 Minutes
  • Global
From
Project Management as applied to Clinical Trials (Recorded) - Product Thumbnail Image

Project Management as applied to Clinical Trials (Recorded)

  • Training
  • April 2024
  • 90 Minutes
  • Global
From
Project Management Process in Development of In Vitro Diagnostics (Recorded) - Product Thumbnail Image

Project Management Process in Development of In Vitro Diagnostics (Recorded)

  • Training
  • April 2024
  • 90 Minutes
  • Global
From
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