QbD & Method Development
Liquid ChromatographyPharmaceuticalPharmaceutical RegulationsQbD & Method DevelopmentWebinarsPetra Lewits and Egidijus Machtejevas (Merck KGaA, Darmstadt, Germany)

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

On-Demand
Learn about the principles and importance of U/HPLC method adaptation in pharmaceutical analysis and how to boost laboratory effectiveness and efficiency.

PharmaceuticalPharmaceutical RegulationsProcess Analytical Technology & Continuous ManufacturingQbD & Method DevelopmentBlogsExpert ForumsPharma 4.0 - Transforming Pharmaceutical Manufacturing

Join Pharma 4.0 – 2021 – Transforming Pharmaceutical Manufacturing

PHARMA 4.0: Transforming Pharmaceutical Manufacturing has been created to help the scientific community address the challenges by creating opportunities for knowledge exchange and expert learning, as well...

PharmaceuticalPharmaceutical RegulationsProcess Analytical Technology & Continuous ManufacturingQbD & Method DevelopmentBlogsExpert ForumsPharma 4.0 - Transforming Pharmaceutical Manufacturing

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

With the move from traditional batch manufacturing to continuous manufacturing, there is a need for real-time monitoring and real-time release of products, webinar by Peter Van Broeck,...

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