+353-1-416-8900REST OF WORLD
+44-20-3973-8888REST OF WORLD
1-917-300-0470EAST COAST U.S
1-800-526-8630U.S. (TOLL FREE)

Pharmaceutical Manufacturing Market Research Reports

21 CFR Part 111 - Current FDA 483 Observations and Warning Letters Review - State of the Dietary Supplement Industry - Webinar (Recorded) - Product Thumbnail Image

21 CFR Part 111 - Current FDA 483 Observations and Warning Letters Review - State of the Dietary Supplement Industry - Webinar (Recorded)

  • Webinar
  • February 2022
  • 60 Minutes
  • Global
Global Fill Finish Manufacturing Market Outlook 2021-2031 - Product Thumbnail Image

Global Fill Finish Manufacturing Market Outlook 2021-2031

  • Report
  • February 2022
  • 209 Pages
  • Global
From
Europe Pharmaceutical Contract Development and Manufacturing Organization (CDMO) Market Outlook 2020-2030 - Product Thumbnail Image

Europe Pharmaceutical Contract Development and Manufacturing Organization (CDMO) Market Outlook 2020-2030

  • Report
  • January 2022
  • 243 Pages
  • Europe
From
Lifecycle Management of Analytical Methods and Procedures according to new USP and ICH Guidelines (Recorded) - Product Thumbnail Image

Lifecycle Management of Analytical Methods and Procedures according to new USP and ICH Guidelines (Recorded)

  • Training
  • December 2021
  • 2 Days
  • Global
From
21 CFR Part 11, Data Integrity, and Computer System Validation (Recorded) - Product Thumbnail Image

21 CFR Part 11, Data Integrity, and Computer System Validation (Recorded)

  • Training
  • September 2021
  • 1 Day
  • Global
From
Analytical Method Validation, Verification and Transfer (Recorded) - Product Thumbnail Image

Analytical Method Validation, Verification and Transfer (Recorded)

  • Training
  • March 2021
  • 2 Days
  • Global
From
CFR/ICH GCP Reference Guide for Medical Devices 2020 - Product Thumbnail Image

CFR/ICH GCP Reference Guide for Medical Devices 2020

  • Book
  • January 2020
  • 378 Pages
Computer System Validation (CSV) and Data Integrity for Clinical Trials Regulated by FDA - Webinar (Recorded) - Product Thumbnail Image

Computer System Validation (CSV) and Data Integrity for Clinical Trials Regulated by FDA - Webinar (Recorded)

  • Webinar
  • October 2019
  • 3 Hours
  • Global
From
Analytical Method Validation and Transfer According to the New FDA Guidance - Webinar (Recorded) - Product Thumbnail Image

Analytical Method Validation and Transfer According to the New FDA Guidance - Webinar (Recorded)

  • Webinar
  • May 2019
  • 90 Minutes
  • Global
Establishing a Robust Data Integrity Program - Webinar (Recorded) - Product Thumbnail Image

Establishing a Robust Data Integrity Program - Webinar (Recorded)

  • Webinar
  • February 2019
  • 90 Minutes
  • Global
Tools for Human Error Reduction: Developing Metrics and KPI's (Key Performance Indicators) to Minimize Human Rrror Rates - Webinar (Recorded) - Product Thumbnail Image

Tools for Human Error Reduction: Developing Metrics and KPI's (Key Performance Indicators) to Minimize Human Rrror Rates - Webinar (Recorded)

  • Webinar
  • May 2018
  • 180 Pages
  • Global
From
Streamlining your QMS and Audit System for Remote Audits - Product Thumbnail Image

Streamlining your QMS and Audit System for Remote Audits

  • Training
  • 60 Minutes
  • Global
DEA, Your Registration and How to Lose It - Product Thumbnail Image

DEA, Your Registration and How to Lose It

  • Training
  • 120 Minutes
  • Global
Learning from Recent FDA Warning Letters Related to Part 11 and Computer Validation - Product Thumbnail Image

Learning from Recent FDA Warning Letters Related to Part 11 and Computer Validation

  • Training
  • 75 Minutes
  • Global
Auditing API Facilities: A MUST to properly prepare for an FDA Regulatory API GMP Inspection - Product Thumbnail Image

Auditing API Facilities: A MUST to properly prepare for an FDA Regulatory API GMP Inspection

  • Training
  • 60 Minutes
  • Global
ICH Stability Requirements and Challenges - Product Thumbnail Image

ICH Stability Requirements and Challenges

  • Training
  • 60 Minutes
  • Global
Equipment Cleaning Validation - Program Setup, Monitoring to Meet FDA Expectations - Product Thumbnail Image

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

  • Training
  • 60 Minutes
  • Global
Risk Based Monitoring for GCP Compliance - Product Thumbnail Image

Risk Based Monitoring for GCP Compliance

  • Training
  • 60 Minutes
  • Global
Electronic Submissions to the FDA - eCTD Requirements - Product Thumbnail Image

Electronic Submissions to the FDA - eCTD Requirements

  • Training
  • 60 Minutes
  • Global
Aseptic Processing Overview and Validation - Product Thumbnail Image

Aseptic Processing Overview and Validation

  • Training
  • 90 Minutes
  • Global
Loading Indicator

The Pharmaceutical Manufacturing market is composed of companies that produce drugs and other pharmaceutical products. These products are used to treat and prevent diseases, as well as to improve the quality of life. Pharmaceutical manufacturers are responsible for the research, development, production, and distribution of these products. They must adhere to strict regulations and standards to ensure the safety and efficacy of their products. The Pharmaceutical Manufacturing market is highly competitive, with many large companies vying for market share. Some of the major players in the market include Pfizer, Merck, Johnson & Johnson, Novartis, and GlaxoSmithKline. These companies are involved in the research, development, production, and distribution of pharmaceutical products. They are also involved in the marketing and promotion of their products. Show Less Read more