Pharmaceutical Regulations

Featured Gas Chromatography Pharmaceutical Pharmaceutical Regulations Quality Assurance & Quality Control Application Notes Separation Science in collaboration with Agilent

Residual Solvents Analysis for the Pharmaceutical Industry

By Separation Science in collaboration with Agilent | Dec 9, 2024

Discover methods to meet USP <467> standards, streamline workflows, and achieve precise, reproducible solvent analysis in real-world conditions.

Environmental Food & Beverage Food Regulations Persistent Organic Pollutants Pharmaceutical Pharmaceutical Regulations Expert Forums Separation Science in collaboration with the life science business of Merck KGaA, Darmstadt, Germany and Mettler-Toledo

Expanding PFAS Analysis Beyond Environmental Matrices

By Separation Science in collaboration with the life science business of Merck KGaA, Darmstadt, Germany and Mettler-Toledo | Nov 2, 2023

Extractables & Leachables Impurity Analysis Pharmaceutical Pharmaceutical Regulations eBooks Separation Science in collaboration with Agilent

The Expert’s Guide to Pharmaceutical Impurity Analysis

By Separation Science in collaboration with Agilent | Oct 30, 2023

DMPK & ADME-Tox Environmental Impurity Analysis Persistent Organic Pollutants Pharmaceutical Pharmaceutical Regulations Quality Assurance & Quality Control Articles Thought Leadership Aimee Cichocki

PFAS in Pharmaceuticals: An Evolving Regulatory Landscape

By Aimee Cichocki | Oct 9, 2023

PFAS in pharma

Liquid Chromatography Pharmaceutical Pharmaceutical Regulations Titration Webinars Separation Science in collaboration with Mettler-Toledo

How to Fulfil Regulatory Compliance with Your Karl Fischer Titration Process

By Separation Science in collaboration with Mettler-Toledo | Oct 5, 2023

Liquid Chromatography Pharmaceutical Pharmaceutical Regulations QbD & Method Development Webinars Petra Lewits and Egidijus Machtejevas (Merck KGaA, Darmstadt, Germany)

Leverage the full potential of Pharmacopeia regulated U/HPLC method adaptation to increase lab effectiveness

By Petra Lewits and Egidijus Machtejevas (Merck KGaA, Darmstadt, Germany) | Sep 22, 2023

Pharmaceutical Pharmaceutical Regulations Process Analytical Technology & Continuous Manufacturing QbD & Method Development Quality Assurance & Quality Control Blogs Expert Forums Pharma 4.0 - Transforming Pharmaceutical Manufacturing

Regulatory Challenges in Pharma 4.0

By Pharma 4.0 - Transforming Pharmaceutical Manufacturing | Jul 6, 2022

Pharmaceutical Pharmaceutical Regulations Process Analytical Technology & Continuous Manufacturing QbD & Method Development Blogs Expert Forums Pharma 4.0 - Transforming Pharmaceutical Manufacturing

Impact of COVID on Pharma 4.0

By Pharma 4.0 - Transforming Pharmaceutical Manufacturing | Jul 6, 2022

Pharmaceutical Pharmaceutical Regulations Process Analytical Technology & Continuous Manufacturing QbD & Method Development Blogs Expert Forums Pharma 4.0 - Transforming Pharmaceutical Manufacturing

Pharma 4.0: Analytical Procedure Lifecycle Management

By Pharma 4.0 - Transforming Pharmaceutical Manufacturing | Nov 18, 2021

Pharmaceutical Pharmaceutical Regulations Process Analytical Technology & Continuous Manufacturing QbD & Method Development Blogs Expert Forums Pharma 4.0 - Transforming Pharmaceutical Manufacturing

Pharma 4.0 – 2021: Streamlining Biologics Production

By Pharma 4.0 - Transforming Pharmaceutical Manufacturing | Nov 4, 2021

Pharmaceutical Pharmaceutical Regulations Process Analytical Technology & Continuous Manufacturing QbD & Method Development Blogs Expert Forums Pharma 4.0 - Transforming Pharmaceutical Manufacturing

Join Pharma 4.0 – 2021 – Transforming Pharmaceutical Manufacturing

By Pharma 4.0 - Transforming Pharmaceutical Manufacturing | Sep 23, 2021

Pharmaceutical

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