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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.

Quality Control Laboratory Compliance - cGMP and GLP Training (Recorded) - Product Thumbnail Image

Quality Control Laboratory Compliance - cGMP and GLP Training (Recorded)

  • Training
  • May 2024
  • 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
SOP Synergy 2023 - Writing Effective Standard Operating Procedures Seminar (Recorded) - Product Thumbnail Image

SOP Synergy 2023 - Writing Effective Standard Operating Procedures Seminar (Recorded)

  • Training
  • February 2024
  • 2 Days
  • Global
From
Effective SOP Writing Masterclass - Training and Compliance in the Pharmaceutical Industry (Recorded) - Product Thumbnail Image

Effective SOP Writing Masterclass - Training and Compliance in the Pharmaceutical Industry (Recorded)

  • Training
  • April 2024
  • 2 Days
  • Global
From
Statistical Elements of Implementing ICH Quality Guidelines (Recorded) - Product Thumbnail Image

Statistical Elements of Implementing ICH Quality Guidelines (Recorded)

  • Training
  • February 2024
  • 2 Days
  • Global
From
The FDA QMSR and the Key Elements of QSIT cGMP Inspection and Audits for Medical Device Manufacturers (Recorded) - Product Thumbnail Image

The FDA QMSR and the Key Elements of QSIT cGMP Inspection and Audits for Medical Device Manufacturers (Recorded)

  • Training
  • February 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
Internal and External / Supplier Audits Essentials (Recorded) - Product Thumbnail Image

Internal and External / Supplier Audits Essentials (Recorded)

  • Training
  • April 2024
  • 2 Days
  • Global
From
A TO Z OF Analytical Method Validation, Verification and Transfer (Recorded) - Product Thumbnail Image

A TO Z OF Analytical Method Validation, Verification and Transfer (Recorded)

  • Training
  • March 2024
  • 2 Days
  • 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
  • Europe, United States Europe, United States
From
eCTD Submissions - Fundamentals and Process (Recorded) - Product Thumbnail Image

eCTD Submissions - Fundamentals and Process (Recorded)

  • Training
  • February 2024
  • 60 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
Risk-Based Excel Spreadsheet Validation (Recorded) - Product Thumbnail Image

Risk-Based Excel Spreadsheet Validation (Recorded)

  • Training
  • March 2024
  • 90 Minutes
  • Global
From
Good Clinical Practices (GCP) Audit and Inspection Readiness (Recorded) - Product Thumbnail Image

Good Clinical Practices (GCP) Audit and Inspection Readiness (Recorded)

  • Training
  • March 2024
  • 90 Minutes
  • Global
From
Designing Effective and Efficient Extractables or Leachables Studies (Recorded) - Product Thumbnail Image

Designing Effective and Efficient Extractables or Leachables Studies (Recorded)

  • Training
  • March 2024
  • 90 Minutes
  • Global
From
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