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World Compliance Seminar - Market Research Reports

WCS Consulting Inc. provide Custom Corporate Training, onsite Business Seminars and Employee Development Workshops designed to improve employee & company performance.

Regulatory Compliance Mastery: Dietary Supplements in North America and Europe (Recorded) - Product Thumbnail Image

Regulatory Compliance Mastery: Dietary Supplements in North America and Europe (Recorded)

  • Training
  • February 2025
  • 2 Days
  • North America, Europe North America, Europe
From
The Drug Development Process: An Intensive 2 Day Training Online (Recorded) - Product Thumbnail Image

The Drug Development Process: An Intensive 2 Day Training Online (Recorded)

  • Training
  • March 2025
  • 2 Days
  • Global
From
FDA Regulatory Compliance for Drug and Biotech Product Training Course (Recorded) - Product Thumbnail Image

FDA Regulatory Compliance for Drug and Biotech Product Training Course (Recorded)

  • Training
  • March 2025
  • 2 Days
  • Global
From
Analytical Method Validation, Verification and Transfer Virtual Seminar (Recorded) - Product Thumbnail Image

Analytical Method Validation, Verification and Transfer Virtual Seminar (Recorded)

  • Training
  • February 2025
  • 2 Days
  • Global
From
Medical Devices: Developing Effective Post Market Surveillance and Complaint Handling Systems (Recorded) - Product Thumbnail Image

Medical Devices: Developing Effective Post Market Surveillance and Complaint Handling Systems (Recorded)

  • Training
  • February 2025
  • 2 Days
  • Global
From
Global Regulatory Requirements for Drug Safety & Pharmacovigilance Certification Program (Recorded) - Product Thumbnail Image

Global Regulatory Requirements for Drug Safety & Pharmacovigilance Certification Program (Recorded)

  • Training
  • February 2025
  • 3 Hours
  • Global
From
Raw Material Requirements (Health Canada/USP/EP) in a cGMP Environment - Issues and Solutions Training Course (Recorded) - Product Thumbnail Image

Raw Material Requirements (Health Canada/USP/EP) in a cGMP Environment - Issues and Solutions Training Course (Recorded)

  • Training
  • February 2025
  • 2 Days
  • Global
From
Efficient Batch Record Design and Review (Recorded) - Product Thumbnail Image

Efficient Batch Record Design and Review (Recorded)

  • Training
  • February 2025
  • 2 Days
  • Global
From
Process Validation for Pharmaceutical and Biologics (Recorded) - Product Thumbnail Image

Process Validation for Pharmaceutical and Biologics (Recorded)

  • Training
  • February 2025
  • 2 Days
  • Global
From
cGMP Regulatory Inspections - Through the Eyes of FDA, EMA and PMDA (Recorded) - Product Thumbnail Image

cGMP Regulatory Inspections - Through the Eyes of FDA, EMA and PMDA (Recorded)

  • Training
  • March 2025
  • 3 Hours
  • Global
From
Aseptic Processing of Pharmaceutical and Biotech Products (Recorded) - Product Thumbnail Image

Aseptic Processing of Pharmaceutical and Biotech Products (Recorded)

  • Training
  • March 2025
  • 2 Days
  • Global
From
Mastering Pharmaceutical Document Management: Strategies for Compliance and Efficiency (Recorded) - Product Thumbnail Image

Mastering Pharmaceutical Document Management: Strategies for Compliance and Efficiency (Recorded)

  • Training
  • March 2025
  • 3 Days
  • Global
From
Effective Technical Writing Course (Recorded) - Product Thumbnail Image

Effective Technical Writing Course (Recorded)

  • Training
  • March 2025
  • 3 Days
  • Global
From
Project Management for Non-Project Managers - PM in the Life Sciences - Pharmaceutical/Biotechnology and Medical Devices (Recorded) - Product Thumbnail Image

Project Management for Non-Project Managers - PM in the Life Sciences - Pharmaceutical/Biotechnology and Medical Devices (Recorded)

  • Training
  • March 2025
  • 2 Days
  • Global
From
Generative AI in Drug Discovery (Recorded) - Product Thumbnail Image

Generative AI in Drug Discovery (Recorded)

  • Training
  • April 2025
  • 1 Day
  • Global
From
FDA Compliance and Clinical Trial Computer System Validation Core Requirements, Expectations and Challenges (Recorded) - Product Thumbnail Image

FDA Compliance and Clinical Trial Computer System Validation Core Requirements, Expectations and Challenges (Recorded)

  • Training
  • April 2025
  • 2 Days
  • Global
From
Master Validation Plan - The Unwritten Requirements Course (Recorded) - Product Thumbnail Image

Master Validation Plan - The Unwritten Requirements Course (Recorded)

  • Training
  • April 2025
  • 3 Hours
  • Global
From
Raw Material Requirements (Health Canada/USP/EP) in a cGMP Environment - Issues and Solutions Training Course (Recorded) - Product Thumbnail Image

Raw Material Requirements (Health Canada/USP/EP) in a cGMP Environment - Issues and Solutions Training Course (Recorded)

  • Training
  • November 2024
  • 2 Days
  • Global
From
Aseptic Processing of Pharmaceutical and Biotech Products Course (Recorded) - Product Thumbnail Image

Aseptic Processing of Pharmaceutical and Biotech Products Course (Recorded)

  • Training
  • November 2024
  • 2 Days
  • Global
From
cGMP Regulatory Inspections - Through the Eyes of FDA, EMA and PMDA (Recorded) - Product Thumbnail Image

cGMP Regulatory Inspections - Through the Eyes of FDA, EMA and PMDA (Recorded)

  • Training
  • November 2024
  • 1 Day
  • Global
From
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