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

World Compliance Seminar - Webinars, Training & Conferences

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

Implementing CSA for GxP Systems - Transition, Documentation, and Post-Transition Challenges and Opportunities (Recorded) - Product Thumbnail Image

Implementing CSA for GxP Systems - Transition, Documentation, and Post-Transition Challenges and Opportunities (Recorded)

  • Training
  • October 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
  • November 2025
  • 3 Hours
  • Global
From
Design History File (DHF), Device Master Record (DMR), and Device History Record (DHR) for Medical Devices Training (Recorded) - Product Thumbnail Image

Design History File (DHF), Device Master Record (DMR), and Device History Record (DHR) for Medical Devices Training (Recorded)

  • Training
  • November 2025
  • 4 Hours
  • Global
From
Biopharmaceutical Manufacturing Process Validation (Recorded) - Product Thumbnail Image

Biopharmaceutical Manufacturing Process Validation (Recorded)

  • Training
  • November 2025
  • 2 Days
  • Global
From
Biostatistics for the Non-Statistician Training Course (Recorded) - Product Thumbnail Image

Biostatistics for the Non-Statistician Training Course (Recorded)

  • Training
  • October 2025
  • 3 Days
  • Global
From
Statistical Process Control (SPC) An Exercise-Based Training Course (Recorded) - Product Thumbnail Image

Statistical Process Control (SPC) An Exercise-Based Training Course (Recorded)

  • Training
  • October 2025
  • 6 Hours
  • Global
From
Human Error Prevention (HEP) - Risk Factors and Strategies (December 15, 2025) - Product Thumbnail Image

Human Error Prevention (HEP) - Risk Factors and Strategies (December 15, 2025)

  • Training
  • December 2025
  • 1 Day
  • Global
From
GMP Auditing for Quality Assurance Training Course for FDA Regulated Industries (Recorded) - Product Thumbnail Image

GMP Auditing for Quality Assurance Training Course for FDA Regulated Industries (Recorded)

  • Training
  • October 2025
  • 2 Days
  • Global
From
Auditing and Qualifying Suppliers and Vendors Course - An Effective Risk Based Approach (Recorded) - Product Thumbnail Image

Auditing and Qualifying Suppliers and Vendors Course - An Effective Risk Based Approach (Recorded)

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

Supplier And Contract Manufacturer Management Course (Recorded)

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

Global Regulatory Requirements for Drug Safety & Pharmacovigilance (Recorded)

  • Training
  • November 2025
  • 3 Hours
  • Global
From
FDA Recalls - Before You Start, and After You Finish (Recorded) - Product Thumbnail Image

FDA Recalls - Before You Start, and After You Finish (Recorded)

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

Process Validation for Pharmaceutical and Biologics (Recorded)

  • Training
  • October 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
  • November 2025
  • 3 Hours
  • Global
From
How to Write Effective Standard Operating Procedures (SOPs) and Other Process Documents Course (Recorded) - Product Thumbnail Image

How to Write Effective Standard Operating Procedures (SOPs) and Other Process Documents Course (Recorded)

  • Training
  • November 2025
  • 3 Days
  • Global
From
Computerized Systems Validation, Data Integrity & Cloud Computing In Pharma & Biotech (Recorded) - Product Thumbnail Image

Computerized Systems Validation, Data Integrity & Cloud Computing In Pharma & Biotech (Recorded)

  • Training
  • December 2025
  • 2 Days
  • Global
From
Computer System Validation Training Boot Camp®: Master FDA, EMA, and GAMP 5 Computer System Validation Requirements (December 9-11, 2025) - Product Thumbnail Image

Computer System Validation Training Boot Camp®: Master FDA, EMA, and GAMP 5 Computer System Validation Requirements (December 9-11, 2025)

  • Training
  • December 2025
  • 3 Days
  • Global
From
Intro to Medical Device Submission - 510(k)s, PMAs & Exemptions (Recorded) - Product Thumbnail Image

Intro to Medical Device Submission - 510(k)s, PMAs & Exemptions (Recorded)

  • Training
  • October 2025
  • 3 Hours
  • Global
US FDA Medical Device Quality System (QSR) Compliance: Design Controls, Verification & Validation (Recorded) - Product Thumbnail Image

US FDA Medical Device Quality System (QSR) Compliance: Design Controls, Verification & Validation (Recorded)

  • Training
  • October 2025
  • 2 Days
  • United States
From
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