+353-1-416-8900REST OF WORLD
+44-20-3973-8888REST OF WORLD
1-917-300-0470EAST COAST U.S
1-800-526-8630U.S. (TOLL FREE)

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.

Corrective Actions Preventive Actions - CAPA 101 (Recorded) - Product Thumbnail Image

Corrective Actions Preventive Actions - CAPA 101 (Recorded)

  • Training
  • August 2025
  • 60 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
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
GLP Laboratory Compliance Documentation and Recordkeeping (Recorded) - Product Thumbnail Image

GLP Laboratory Compliance Documentation and Recordkeeping (Recorded)

  • Training
  • July 2025
  • 2 Days
  • Global
From
Statistical Methods for Process Validation (Recorded) - Product Thumbnail Image

Statistical Methods for Process Validation (Recorded)

  • Training
  • September 2025
  • 60 Minutes
  • Global
From
How to Reduce Human Error in a GMP Manufacturing Floor (Recorded) - Product Thumbnail Image

How to Reduce Human Error in a GMP Manufacturing Floor (Recorded)

  • Training
  • September 2025
  • 90 Minutes
  • Global
From
21 CFR Part 11 Data Integrity Training for CSV, CSA, SaaS/Cloud - How to Reduce Costs for Compliance (Recorded) - Product Thumbnail Image

21 CFR Part 11 Data Integrity Training for CSV, CSA, SaaS/Cloud - How to Reduce Costs for Compliance (Recorded)

  • Training
  • January 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
CSV vs CSA - Waterfall vs. Agile Methodology, Documentation and Implementation (Recorded) - Product Thumbnail Image

CSV vs CSA - Waterfall vs. Agile Methodology, Documentation and Implementation (Recorded)

  • Training
  • April 2024
  • 2 Days
  • Global
From
3-Hour Virtual Seminar on US FDA and EU Medical Device Directive Requirements for DHF, DMR, DHR and TF/DDS (Recorded) - Product Thumbnail Image

3-Hour Virtual Seminar on US FDA and EU Medical Device Directive Requirements for DHF, DMR, DHR and TF/DDS (Recorded)

  • Training
  • March 2024
  • 3 Hours
  • United States, Europe United States, Europe
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 Successful Deviation Investigations (Recorded) - Product Thumbnail Image

3-Hour Virtual Seminar on Successful Deviation Investigations (Recorded)

  • Training
  • January 2024
  • 3 Hours
  • 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
GMP Microbiology Training - Pack of 12 webinars - Product Thumbnail Image

GMP Microbiology Training - Pack of 12 webinars

  • Training
  • 15 Hours
  • Global
Loading Indicator