Analytical Instrumentation & Methodology Whitepapers
This white paper discusses drug formulation including novel drug delivery systems, the pros and cons of certain drug forms and the challenges of developing a NDDS.
|Extractables & Leachables
This white paper discusses the basics of Extractables & Leachables testing as it used within drug manufacturing and packaging.
|E&L Challenges for Pharmaceutical Manufacturing
This whitepaper provides guidance on thecommon extractables and leachables (E&L) challenges that pharmaceutical drug manufacturing and development companies face.
|Analytical Methodology for CMC Whitepaper
Information about the process of method development and validation for pharmaceutical drug products. Learn the steps necessary to develop the methods required to measure identity and purity attributes and more. Read the full whitepaper from Avomeen Life Sciences.
Appropriate Methods When Developing Novel Biologics Biologics, especially protein therapeutics, are an intriguing and fast-growing market for biopharmaceutical companies of all sizes. Learn more.
|Cleaning Validation Whitepaper
Information about the unique requirements of cleaning validation for biopharmaceuticals. Learn about sampling considerations, inspections and the applicable regulations . Read the full whitepaper from Avomeen Life Sciences.
|IP & Legal Support Whitepaper
Learn more about the intersection of chemical analysis and intellectual property disputes in Biopharmaceuticals. Read the full whitepaper from Avomeen Life Sciences.
Information about novel drug delivery systems. Learn about how advanced formulation services can improve your product or extend a product’s life cycle. Read the full whitepaper from Avomeen Analytical Services.
|Stability Testing Whitepaper
Information about both CDER & CDRH stability testing programs and their specific regulations. Learn more in our extensive whitepaper.
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