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Learn about what sets GMP and cGMP apart, and how to choose the best compliance standard for your product.
After a complete revision of the EU GMP Annex 1, the final version was published in August 2022 and became effective just a few days ago on August 25,…
Proven Process to Optimize Commercial Readiness
The key to successful development and guiding a drug to approval is early planning.
Fast, safe and efficient: the new Vetter ID determination of oligonucleotides.
Interview with Oskar Gold, SVP Asia Pacific and Global Emerging Markets
Why double-bagged tubs are an issue for high-speed filling lines
A CDMO’s Guide to Digitalization in the Pharmaceutical Industry
A Holistic Cleanroom Concept: Higher Quality and Greater Flexibility
Why CDMOs are increasingly vital to successful drug development
How small production quantities are growing in importance
Five key considerations we share with companies who are deciding where and when to make key decisions about their secondary packaging strategy.