Pharmaceutical Regulations

Extractables & Leachables Impurity Analysis Pharmaceutical Pharmaceutical Regulations Quality Assurance & Quality Control Digital Magazines Separation Science

Pharmaceutical Purity and Precision

By Separation Science | May 2, 2024

Find out what’s happening in the world of pharmaceutical impurity analysis and learn about the latest topics and techniques.

Liquid Chromatography Pharmaceutical Pharmaceutical Regulations Articles Separation Science in collaboration with the life science business of Merck KGaA, Darmstadt, Germany

Tips & Tricks for IC: A Quick Overview on IQ/ OQ/PV(PQ) of Ion Chromatography Instruments

By Separation Science in collaboration with the life science business of Merck KGaA, Darmstadt, Germany | May 1, 2024

Impurity Analysis Pharmaceutical Pharmaceutical Regulations Articles Jack Steed

Overcoming the Challenges of Nitrosamine Analysis Using LC-MS/MS

By Jack Steed | Apr 24, 2024

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

Continuous Manufacturing: Business Case Drivers, Control and Deployment Strategies for Small Molecule Oral Products

By Pharma 4.0 - Transforming Pharmaceutical Manufacturing | Mar 25, 2021

Pharmaceutical

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