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Results for tag: "GMP"

Advanced Therapy Medicinal Products CDMO Market Size, Share & Industry Trends Analysis Report By Indication, By Product, By Phase, By Regional Outlook and Forecast, 2022-2028 - Product Thumbnail Image

Advanced Therapy Medicinal Products CDMO Market Size, Share & Industry Trends Analysis Report By Indication, By Product, By Phase, By Regional Outlook and Forecast, 2022-2028

  • Report
  • January 2023
  • 282 Pages
  • Global
From
Quality and Compliance Management for Virtual Companies (Recorded) - Product Thumbnail Image

Quality and Compliance Management for Virtual Companies (Recorded)

  • Training
  • July 2024
  • 2 Days
  • Global
Managing Microbiological Out of Specification (OOS) and Out of Trend (OOT) Results in Sterile and Non-Sterile Production FDA & ICH Expectations and Guidance (Recorded) - Product Thumbnail Image

Managing Microbiological Out of Specification (OOS) and Out of Trend (OOT) Results in Sterile and Non-Sterile Production FDA & ICH Expectations and Guidance (Recorded)

  • Training
  • July 2024
  • 90 Minutes
  • Global
Process Validation Guidance Requirements Course (FDA and EU Annex 15: Qualifications and Validation) (Recorded) - Product Thumbnail Image

Process Validation Guidance Requirements Course (FDA and EU Annex 15: Qualifications and Validation) (Recorded)

  • Training
  • July 2024
  • 2 Days
  • Global
From
FDA Inspection (Recorded) - Product Thumbnail Image

FDA Inspection (Recorded)

  • Training
  • June 2024
  • 2 Days
  • Global
From
3hr Virtual Seminar - Validation, Verification and Transfer of Analytical Methods - Implementing Guidelines from FDA/EMA, USP and ICH - Product Thumbnail Image

3hr Virtual Seminar - Validation, Verification and Transfer of Analytical Methods - Implementing Guidelines from FDA/EMA, USP and ICH

  • Training
  • 3 Hours
  • Global
Aseptic Processing Of Pharmaceutical and Biotech Products (Recorded) - Product Thumbnail Image

Aseptic Processing Of Pharmaceutical and Biotech Products (Recorded)

  • Training
  • August 2024
  • 2 Days
  • Global
From
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
GMP Auditing of Active Pharmaceutical Ingredients (APIs) and Excipient Suppliers (Recorded) - Product Thumbnail Image

GMP Auditing of Active Pharmaceutical Ingredients (APIs) and Excipient Suppliers (Recorded)

  • Training
  • March 2024
  • 6 Hours
  • 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
Process Validation Training Course (FDA and EU Annex 15: Qualifications and Validation) (Recorded) - Product Thumbnail Image

Process Validation Training Course (FDA and EU Annex 15: Qualifications and Validation) (Recorded)

  • Training
  • January 2024
  • 2 Days
  • Global
From
Enhancing Quality Oversight in Pharmaceutical Contract Manufacturing Organizations (Recorded) - Product Thumbnail Image

Enhancing Quality Oversight in Pharmaceutical Contract Manufacturing Organizations (Recorded)

  • Training
  • August 2023
  • 2 Days
  • Global
From
Europe - Pharmaceuticals, Major Manufacturers Map - 5th Edition - Product Thumbnail Image

Europe - Pharmaceuticals, Major Manufacturers Map - 5th Edition

  • Map
  • November 2022
  • Europe
From
Master Raw Material Compliance in Pharmaceuticals: Health Canada, USP & EP Standards - 2-Day Virtual Seminar (November 20-21, 2025) - Product Thumbnail Image

Master Raw Material Compliance in Pharmaceuticals: Health Canada, USP & EP Standards - 2-Day Virtual Seminar (November 20-21, 2025)

  • Training
  • November 2025
  • 2 Days
  • Canada
From
cGMP Regulatory Inspections - Through the Eyes of FDA, EMA and PMDA (November 13, 2025) - Product Thumbnail Image

cGMP Regulatory Inspections - Through the Eyes of FDA, EMA and PMDA (November 13, 2025)

  • Training
  • November 2025
  • 3 Hours
  • Global
From
Data Integrity in GMP and GCP: Compliance with FDA, EMA, and MHRA Requirements (Recorded) - Product Thumbnail Image

Data Integrity in GMP and GCP: Compliance with FDA, EMA, and MHRA Requirements (Recorded)

  • Training
  • October 2025
  • 60 Minutes
  • Global
From
Mapping and Review of Pharmaceutical Manufacturing and Packaging Workflows (Recorded) - Product Thumbnail Image

Mapping and Review of Pharmaceutical Manufacturing and Packaging Workflows (Recorded)

  • Training
  • August 2025
  • 90 Minutes
  • Global
From
GMP Training for the QC Laboratory (Recorded) - Product Thumbnail Image

GMP Training for the QC Laboratory (Recorded)

  • Training
  • October 2024
  • 2 Days
  • Global
From
Annual Current Good Manufacturing Practices (cGMP) Training (Recorded) - Product Thumbnail Image

Annual Current Good Manufacturing Practices (cGMP) Training (Recorded)

  • Training
  • June 2024
  • 60 Minutes
  • Global
Risk-Based Approach to CSV, 21 CFR Part 11 and FDA Compliance (Recorded) - Product Thumbnail Image

Risk-Based Approach to CSV, 21 CFR Part 11 and FDA Compliance (Recorded)

  • Training
  • June 2024
  • 90 Minutes
  • Global
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Good Manufacturing Practice (GMP) is a set of regulations and guidelines that govern the production of pharmaceuticals. GMP is designed to ensure that pharmaceuticals are consistently produced and controlled according to quality standards. It is intended to minimize the risks involved in any pharmaceutical production that cannot be eliminated through testing the final product. GMP covers all aspects of production from the starting materials, premises, and equipment to the training and personal hygiene of staff. Compliance with GMP is mandatory for all manufacturers of pharmaceuticals and active pharmaceutical ingredients. The GMP market is composed of companies that provide services and products related to GMP compliance. These services and products include consulting, auditing, training, and software solutions. Companies in the GMP market include Parexel, SGS, Eurofins, and NSF International. Show Less Read more