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Results for tag: "GMP"

CMO Supplier Quality Agreements - What you need to know to comply with new FDA & EU GMP Guidelines for Contract Drug Manufacture - Webinar (Recorded) - Product Thumbnail Image

CMO Supplier Quality Agreements - What you need to know to comply with new FDA & EU GMP Guidelines for Contract Drug Manufacture - Webinar (Recorded)

  • Webinar
  • February 2023
  • 60 Minutes
  • Europe
From
Water System Biofilm Control and Microbial Monitoring Myths - Webinar (Recorded) - Product Thumbnail Image

Water System Biofilm Control and Microbial Monitoring Myths - Webinar (Recorded)

  • Webinar
  • January 2022
  • 90 Minutes
  • Global
From
Validation and Use of Excel Spreadsheets in FDA Regulated Environments - Webinar (Recorded) - Product Thumbnail Image

Validation and Use of Excel Spreadsheets in FDA Regulated Environments - Webinar (Recorded)

  • Webinar
  • October 2021
  • 75 Minutes
  • Global
From
Human Error Reduction Techniques for Floor Supervisors - Webinar (Recorded) - Product Thumbnail Image

Human Error Reduction Techniques for Floor Supervisors - Webinar (Recorded)

  • Webinar
  • September 2021
  • 90 Minutes
  • Global
From
Developing a Strategic Approach to FDA Compliance for Computer Systems - Product Thumbnail Image

Developing a Strategic Approach to FDA Compliance for Computer Systems

  • Training
  • 90 Minutes
  • Global
Establishing an Effective & Pragmatic Vendor Qualification Program for cGMP Compliance in the Pharmaceutical Industry - Webinar - Product Thumbnail Image

Establishing an Effective & Pragmatic Vendor Qualification Program for cGMP Compliance in the Pharmaceutical Industry - Webinar

  • Webinar
  • 90 Minutes
  • Global
From
How to Ensure Your Foreign Vendors are FDA Compliant: Conducting Vendor Audits, Monitoring, and Using Checklists - Product Thumbnail Image

How to Ensure Your Foreign Vendors are FDA Compliant: Conducting Vendor Audits, Monitoring, and Using Checklists

  • Training
  • 90 Minutes
  • Global
How To Implement An Effective Human Error Reduction Program - Product Thumbnail Image

How To Implement An Effective Human Error Reduction Program

  • Training
  • 90 Minutes
  • Global
Implementing a Robust Data Integrity Program - Product Thumbnail Image

Implementing a Robust Data Integrity Program

  • Training
  • 90 Minutes
  • Global
Process Validation - Overview of Why and How - Product Thumbnail Image

Process Validation - Overview of Why and How

  • Training
  • 60 Minutes
  • Global
Good Practices for Data Integrity, the new Guidance and one FDA Inspector's Experience - Product Thumbnail Image

Good Practices for Data Integrity, the new Guidance and one FDA Inspector's Experience

  • Training
  • 60 Minutes
  • Global
Design History Files and Technical Files/Design Dossiers - Meeting U.S. FDA CGMPS and the EU's MDD Requirements - Product Thumbnail Image

Design History Files and Technical Files/Design Dossiers - Meeting U.S. FDA CGMPS and the EU's MDD Requirements

  • Training
  • 90 Minutes
  • United States, Europe United States, Europe
How to Write Effective 483 and Warning Letter Responses - Product Thumbnail Image

How to Write Effective 483 and Warning Letter Responses

  • Training
  • 90 Minutes
  • Global
Laboratory Inspection Readiness - Implementing GMPs for the Pharmaceutical Laboratory - Product Thumbnail Image

Laboratory Inspection Readiness - Implementing GMPs for the Pharmaceutical Laboratory

  • Training
  • 90 Minutes
  • Global
Effective (FDA Accepted) Responses to FDA-483's and Warning Letters - Product Thumbnail Image

Effective (FDA Accepted) Responses to FDA-483's and Warning Letters

  • Training
  • 60 Minutes
  • Global
Winning Strategies for Successful US FDA Inspections: Conducting an Effective Mock Pre-Approval Inspection & Implementing Robust Remedial Measures - Product Thumbnail Image

Winning Strategies for Successful US FDA Inspections: Conducting an Effective Mock Pre-Approval Inspection & Implementing Robust Remedial Measures

  • Training
  • 90 Minutes
  • United States
How to Prepare for an FDA Inspection? - Product Thumbnail Image

How to Prepare for an FDA Inspection?

  • Training
  • 90 Minutes
  • Global
Implementation and Management of GMP Data Integrity - Product Thumbnail Image

Implementation and Management of GMP Data Integrity

  • Training
  • 90 Minutes
  • Global
Current Good Manufaturing Processes (cGMP) for Pharmaceuticals - E-Learning Course - Product Thumbnail Image

Current Good Manufaturing Processes (cGMP) for Pharmaceuticals - E-Learning Course

  • Training
  • 2 Hours
  • Global
Human Factors and Performance Introduction E-Learning Course - Product Thumbnail Image

Human Factors and Performance Introduction E-Learning Course

  • Training
  • 1 Hour
  • 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