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Results for tag: "Drug Dissolution Testing"

Global Pharmaceutical Dissolution Testing Services Market - Industry Size, Share, Trends, Opportunity, and Forecast, 2018-2028 - Product Thumbnail Image

Global Pharmaceutical Dissolution Testing Services Market - Industry Size, Share, Trends, Opportunity, and Forecast, 2018-2028

  • Report
  • October 2023
  • 170 Pages
  • Global
From
Oral Solid dosage (OSD) Contract Manufacturing Market - Global Industry Size, Share, Trends, Opportunity, and Forecast, 2018-2028F - Product Thumbnail Image

Oral Solid dosage (OSD) Contract Manufacturing Market - Global Industry Size, Share, Trends, Opportunity, and Forecast, 2018-2028F

  • Report
  • November 2023
  • 178 Pages
  • Global
From
AAV Contract Development And Manufacturing Organizations Market Size, Share & Trends Analysis Report By Workflow, By Culture Type, By Application, By End-user, By Region, And Segment Forecasts, 2023 - 2035 - Product Thumbnail Image

AAV Contract Development And Manufacturing Organizations Market Size, Share & Trends Analysis Report By Workflow, By Culture Type, By Application, By End-user, By Region, And Segment Forecasts, 2023 - 2035

  • Report
  • January 2023
  • 180 Pages
  • Global
From
Pharmaceutical Dissolution Testing Services Market Size, Share & Trends Analysis Report By Method (In Vitro, In Vivo), By Dosage Form (Capsules, Tablets), By Dissolution Apparatus (Basket, Paddle), By Region, And Segment Forecasts, 2023 - 2030 - Product Thumbnail Image

Pharmaceutical Dissolution Testing Services Market Size, Share & Trends Analysis Report By Method (In Vitro, In Vivo), By Dosage Form (Capsules, Tablets), By Dissolution Apparatus (Basket, Paddle), By Region, And Segment Forecasts, 2023 - 2030

  • Report
  • November 2022
  • 120 Pages
  • Global
From
New Elemental Impurities Tests for Pharmaceutical Products According to the New ICH Q3D and USP 232/233 Guidelines - Webinar (Recorded) - Product Thumbnail Image

New Elemental Impurities Tests for Pharmaceutical Products According to the New ICH Q3D and USP 232/233 Guidelines - Webinar (Recorded)

  • Webinar
  • May 2019
  • 180 Minutes
  • Global
Residual Solvents: Take Advantage of the New Flexibility in Revised USP <467> - Webinar (Recorded) - Product Thumbnail Image

Residual Solvents: Take Advantage of the New Flexibility in Revised USP <467> - Webinar (Recorded)

  • Webinar
  • January 2018
  • 90 Minutes
  • Global
Understanding and Applying ICH Q3A and Q3B for Control of Impurities in Drug Substances and Drug Products - Webinar (Recorded) - Product Thumbnail Image

Understanding and Applying ICH Q3A and Q3B for Control of Impurities in Drug Substances and Drug Products - Webinar (Recorded)

  • Webinar
  • December 2020
  • 90 Minutes
  • Global
From
6-Hour Virtual Seminar on Developing a Clinically or Bio- Relevant Drug Dissolution Method and Establishing Plasma Drug Profiles - Webinar (Recorded) - Product Thumbnail Image

6-Hour Virtual Seminar on Developing a Clinically or Bio- Relevant Drug Dissolution Method and Establishing Plasma Drug Profiles - Webinar (Recorded)

  • Webinar
  • April 2020
  • 6 Hours
  • Global
From
Laboratory Inspection Readiness - Implementing GMPs for the Pharmaceutical Laboratory - Webinar (Recorded) - Product Thumbnail Image

Laboratory Inspection Readiness - Implementing GMPs for the Pharmaceutical Laboratory - Webinar (Recorded)

  • Webinar
  • March 2019
  • 120 Minutes
  • Global
Pharmaceutical Dissolution Testing, Bioavailability, and Bioequivalence. Science, Applications, and Beyond. Edition No. 1 - Product Thumbnail Image

Pharmaceutical Dissolution Testing, Bioavailability, and Bioequivalence. Science, Applications, and Beyond. Edition No. 1

  • Book
  • February 2022
  • 560 Pages
Drug Delivery Systems. Advances in Pharmaceutical Product Development and Research - Product Thumbnail Image

Drug Delivery Systems. Advances in Pharmaceutical Product Development and Research

  • Book
  • October 2019
Pharmaceutical Quality by Design. Principles and Applications - Product Thumbnail Image

Pharmaceutical Quality by Design. Principles and Applications

  • Book
  • March 2019
Developing Solid Oral Dosage Forms. Pharmaceutical Theory and Practice. Edition No. 2 - Product Thumbnail Image

Developing Solid Oral Dosage Forms. Pharmaceutical Theory and Practice. Edition No. 2

  • Book
  • November 2016
Aulton's Pharmaceutics. The Design and Manufacture of Medicines. Edition No. 6 - Product Thumbnail Image

Aulton's Pharmaceutics. The Design and Manufacture of Medicines. Edition No. 6

  • Book
  • May 2021
  • 14 Results (Page 1 of 1)
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Drug Dissolution Testing is a critical part of the pharmaceutical industry, as it is used to assess the rate and extent of drug release from a dosage form. It is a process that measures the amount of drug that is released from a dosage form into a liquid medium over a specified period of time. This testing is used to ensure that the drug is released in a consistent manner, and that the drug is safe and effective for use. It is also used to determine the shelf life of a drug, as well as to assess the stability of the drug in different environments. Drug Dissolution Testing is conducted in accordance with the USP and other regulatory guidelines, and is used to ensure that the drug is safe and effective for use. It is also used to assess the bioavailability of the drug, as well as to determine the shelf life of the drug. Some companies in the Drug Dissolution Testing market include Eurofins, Intertek, SGS, and Pharmatech Associates. Show Less Read more