When pharmaceutical companies develop a novel drug for the market, several steps are required to assess and regulate its safety, effectiveness, manufacturability, and reliability. These processes, and ...

LONDON--(BUSINESS WIRE)--The increasing competition of the pharmaceutical industry has encouraged companies to invest in innovation and drug development. However, the drug development process is ...

Designing an efficient platform is crucial for any industrial process. This design process is known as process development, and it has become increasingly important in the pharmaceutical industry at ...

CHARLOTTETOWN, Prince Edward Island--(BUSINESS WIRE)--Today BIOVECTRA celebrates the completion of its $90 million plus biologics expansion at the company’s new state-of-the-art Biomanufacturing ...

To optimize the final formulation for a drug, it must meet many criteria beyond producing a safe and effective product. For example, it must be stable and amenable to various manufacturing steps, such ...

In a Q&A, an FDA spokesperson discusses efforts to reduce misinformation about biosimilars through education, the agency’s collaboration with global regulators to streamline development, and its work ...

When patient safety, regulatory approval and real-world effectiveness are on the line, AI can't act autonomously.

Design & synthesis of novel ionizable POZ lipids to replace current ionizable lipids for the delivery of a multitude of oligonucleotide payloads- HUNTSVILLE, AL, April 07, 2026 (GLOBE NEWSWIRE)-- ...

Several patient and disease advocacy organizations have responded to the Center for Drug Evaluation and Research's (CDER) ...

NEW YORK, Jan. 21 (UPI) --The Food and Drug Administration announced Wednesday that it approved a drug called Quviviq for the treatment of insomnia, a disorder that causes trouble sleeping. The brand ...