Join our API course for an in-depth understanding of active pharmaceutical ingredients in drug manufacturing. Learn the regulatory frameworks of the EU and USA, GMP and GDP practices, and key ...

The U.S. Food and Drug Administration’s (FDA’s) evolving guidance on Computer Software Assurance and AI/ML-Based Software feels like it’s changing faster than you can read it. They’re emphasizing ...

Biosynth, a leading developer and supplier of critical raw materials and services for life sciences and diagnostics, is pleased to announce the opening of its expanded GMP bioconjugation facility at ...

Open House Highlights Expanded Sterile Filling Contract Manufacturing Capabilities for Small and Large Molecules Pace Life Sciences Salem Renderings ...

The USSR built three twin plants. Volkovysk was chosen the venue for a dairy and baby food canning plant. It supplied ...

Exclusive Global Rights: Neurizon is granted exclusive global rights to Elanco’s data package and related intellectual property for monepantel to develop and commercialise NUZ-001 and its related ...

Abeona will receive a license payment and potential development, regulatory, and sales milestones, and royalties ...

The global Pharmaceutical Filtration Market is estimated to be valued at USD 21,643.3 million in 2025 and is projected to reach USD 39,497.5 million by 2035, registering a CAGR of 6.7% over the ...

Meanwhile, Dr. Sami Khalil, Director of the Egyptian Foundation for Drug Research Development (Pharma Group), said that the foundation includes all companies involved in pharmaceutical research.

While the investigation into the June 30 blast is underway, the company said on Wednesday that it was not a reactor explosion ...

Alphalyse, a fast-growing Danish specialist contract research organization (CRO) that has developed GMP‑validated liquid‑chromatography mass‑spectrometry (LC‑MS) assays for host‑cell‑protein (HCP) ...