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Results for tag: "Cleaning Validation"

Pharmaceutical Continuous Manufacturing Market Research Report by Distribution, Application, End User, Region - Global Forecast to 2027 - Cumulative Impact of COVID-19 - Product Thumbnail Image

Pharmaceutical Continuous Manufacturing Market Research Report by Distribution, Application, End User, Region - Global Forecast to 2027 - Cumulative Impact of COVID-19

  • Report
  • July 2022
  • 256 Pages
From
Pharmaceutical Cleaning Validation Market Share, Size, Trends, Industry Analysis Report, By Product; By Test; By Region; Segment Forecast, 2021 - 2028 - Product Thumbnail Image

Pharmaceutical Cleaning Validation Market Share, Size, Trends, Industry Analysis Report, By Product; By Test; By Region; Segment Forecast, 2021 - 2028

  • Report
  • October 2021
  • 113 Pages
From
U.S. Pharmaceutical Analytical Testing Outsourcing Market Size, Share & Trends Analysis Report by Service (Bioanalytical Testing, Method Development & Validation, Stability Testing), by End-use, and Segment Forecasts, 2022-2030 - Product Thumbnail Image

U.S. Pharmaceutical Analytical Testing Outsourcing Market Size, Share & Trends Analysis Report by Service (Bioanalytical Testing, Method Development & Validation, Stability Testing), by End-use, and Segment Forecasts, 2022-2030

  • Report
  • July 2022
  • 84 Pages
From
Total Organic Carbon Analysis for Cleaning Validation in Pharmaceutical Manufacturing - Webinar - Product Thumbnail Image

Total Organic Carbon Analysis for Cleaning Validation in Pharmaceutical Manufacturing - Webinar

  • Webinar
  • February 2019
  • 120 Minutes
From
Global Pharmaceutical Cleaning Validation Market Size, Share & Trends Analysis Report by Product Type (Small Molecule Drug, Proteins, Peptides), by Validation Test, by Region, and Segment Forecasts, 2021-2028 - Product Thumbnail Image

Global Pharmaceutical Cleaning Validation Market Size, Share & Trends Analysis Report by Product Type (Small Molecule Drug, Proteins, Peptides), by Validation Test, by Region, and Segment Forecasts, 2021-2028

  • Report
  • August 2021
  • 126 Pages
From
Aseptic Processing Overview and Validation - Webinar - Product Thumbnail Image

Aseptic Processing Overview and Validation - Webinar

  • Webinar
  • November 2019
  • 120 Minutes
From
Good Laboratory Practices (GLPs) - Comparing and Contrasting with Good Manufacturing Practices (GMPs) - Webinar - Product Thumbnail Image

Good Laboratory Practices (GLPs) - Comparing and Contrasting with Good Manufacturing Practices (GMPs) - Webinar

  • Webinar
  • October 2019
  • 180 Minutes
From
Analytical Method Validation and Transfer - Webinar - Product Thumbnail Image

Analytical Method Validation and Transfer - Webinar

  • Webinar
  • September 2019
  • 120 Minutes
From
Regulatory Inspections - How to prepare for a visit from an FDA Auditor - Webinar - Product Thumbnail Image

Regulatory Inspections - How to prepare for a visit from an FDA Auditor - Webinar

  • Webinar
  • September 2019
  • 120 Minutes
From
Equipment Cleaning Validation - Program Setup, Monitoring to Meet FDA Expectations - Webinar - Product Thumbnail Image

Equipment Cleaning Validation - Program Setup, Monitoring to Meet FDA Expectations - Webinar

  • Webinar
  • April 2018
  • 180 Minutes
From
Equipment Cleaning Validation - Product Thumbnail Image

Equipment Cleaning Validation

  • Training
Allergen Cleaning, Validation & Preventative Risk Management - Webinar - Product Thumbnail Image

Allergen Cleaning, Validation & Preventative Risk Management - Webinar

  • Webinar
  • February 2021
  • 60 Minutes
From
Implementing a Robust Data Integrity Program - Webinar - Product Thumbnail Image

Implementing a Robust Data Integrity Program - Webinar

  • Webinar
  • October 2019
  • 120 Minutes
From
How to Ensure Your Foreign Vendors are FDA Compliant - Conducting Vendor Audits, Monitoring, and Using Checklists - Webinar - Product Thumbnail Image

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

  • Webinar
  • May 2019
  • 120 Minutes
From
How to Write Effective 483 and Warning Letter Responses - Webinar - Product Thumbnail Image

How to Write Effective 483 and Warning Letter Responses - Webinar

  • Webinar
  • March 2019
  • 90 Minutes
From
Designing an Effective Cleaning Validation for Reusable Medical Devices in Today's Regulatory Environment - Webinar - Product Thumbnail Image

Designing an Effective Cleaning Validation for Reusable Medical Devices in Today's Regulatory Environment - Webinar

  • Webinar
  • December 2018
  • 90 Minutes
From
Writing Validation Master Plans: Best Practices for Authoring a Compliant Document - Webinar - Product Thumbnail Image

Writing Validation Master Plans: Best Practices for Authoring a Compliant Document - Webinar

  • Webinar
  • August 2018
  • 90 Minutes
From
Continuous Manufacturing of Pharmaceuticals. Edition No. 1. Advances in Pharmaceutical Technology - Product Thumbnail Image

Continuous Manufacturing of Pharmaceuticals. Edition No. 1. Advances in Pharmaceutical Technology

  • Book
  • September 2017
  • 632 Pages
  • 18 Results (Page 1 of 1)
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