Pharmaceutical Regulations

The image shows pharmaceutical capsules representing stability testing in drug development. It emphasizes analytical techniques critical for evaluating drug stability, shelf-life determination, and maintaining pharmaceutical quality standards.
Articles
| 5 min read
Explore analytical techniques in stability testing, including HPLC, mass spectrometry, and spectroscopy, to ensure product efficacy, safety, and compliance.
Application Notes
Discover methods to meet USP <467> standards, streamline workflows, and achieve precise, reproducible solvent analysis in real-world conditions.
Articles
| 3 min read
Explore the tests that should be part of the instrument qualification process for ion chromatography instruments.
Articles
| 5 min read
Discover how LC-MS/MS can help tackle key challenges in nitrosamine analysis.
Expert Forums

Expanding PFAS Analysis Beyond Environmental Matrices

eBooks

The Expert’s Guide to Pharmaceutical Impurity Analysis

Articles

PFAS in Pharmaceuticals: An Evolving Regulatory Landscape

| 4 min read
Webinars

How to Fulfil Regulatory Compliance with Your Karl Fischer Titration Process

Available On-Demand
Webinars

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

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Blogs

Regulatory Challenges in Pharma 4.0

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Blogs

Impact of COVID on Pharma 4.0

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Blogs

Pharma 4.0: Analytical Procedure Lifecycle Management

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Blogs

Pharma 4.0 - 2021: Streamlining Biologics Production

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Blogs

Join Pharma 4.0 - 2021 - Transforming Pharmaceutical Manufacturing

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Blogs

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

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Blogs

Build the Lab of the Future Today for Pharma 4.0

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Articles

Back-to-Basics #5: Tailing

| 1 min read