Pharmaceutical Manufacturing

This abstract image represents ion mobility as used in IMS-MS, a key technology for nitrosamine detection in pharmaceutical quality control. By visualizing particle separation, it underscores IMS-MS's role in ensuring regulatory compliance and improving impurity profiling.
Articles
| 3 min read
Understand the essentials of QbD for HPLC and create robust, reproducible methods for pharmaceutical applications.
Application Notes
Discover methods to meet USP <467> standards, streamline workflows, and achieve precise, reproducible solvent analysis in real-world conditions.
eBooks
Download this eBook, produced in collaboration with Agilent, to discover the latest regulations, tools, and techniques in pharmaceutical impurity analysis.
Articles
| 4 min read
Examine the regulatory crossroads resulting from the ubiquitous presence of PFAS in widely prescribed drugs.
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Blogs

Nitrosamine Testing using LC-MS Methods from the USP General Chapter <1469>

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Blogs

Analysis of Nucleotide Activated Sugars by LC-MS/MS

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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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Webinars

Dissolution: Today, Tomorrow & Beyond

Available On-Demand
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Webinars

Facilitating Data Integrity & Compliance

Available On-Demand
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Blogs

Pharma 4.0: Analytical Procedure Lifecycle Management

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Blogs

The Importance of Data Integrity in Achieving Pharma 4.0

Available On-Demand
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Blogs

Pharma 4.0 - 2021: Streamlining Biologics Production

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Webinars

Handheld Raman Solutions for Raw Material ID

Available On-Demand