Redica Systems has been assisting pharmaceutical companies in determining GMP quality risks at their manufacturing sites, and with AI, it has a relatively new addition to its toolbox.

Xiao-Yan Cai, PhD, co-founder and CEO of Accurant Biotech, discussed collaborative efforts that must be undertaken between companies, and across scientific disciplines, to work together on continuing ...

The agency’s CHMP recommended drugs to treatments for hemophilia, two biosimilars for psoriasis, and two flu vaccines at their October meeting.

The agency has reconfirmed its recommendation to not give positive opinion to Translarna (ataluren) after a reexamination of the available data.

Regulators, EMA and HMA, have published principles and recommendations on the use of LLMs, which are being increasingly used ...

For the pharmaceutical industry, drug formulation is a cornerstone, crucial for converting bioactive molecules into effective ...

In episode 1, cell and gene therapy experts Dr. Fabian Gerlinghaus, Dr. Claudia Zylberberg, and Benjamin McLeod weigh in on hot topics in CGT. Buy, Sell, Hold is a rapid-fire expert panel covering a ...

Pharmaceutical packaging must advance to adapt to new, complex modalities. Suitable packaging for pharmaceutical products is a must to ensure the integrity of the products is maintained, which ...

Pharmaceutical Technology Europe spoke with John McQuaid, president and managing director at Almac Pharma Services, at CPHI Milan 2024, held October 8–10, in Milan, Italy, about how the pharmaceutical ...

SK pharmteco will be the preferred manufacturing partner for AVG-101, AaviGen’s lead gene therapy product. The California-based contract development and manufacturing organization (CDMO) SK pharmteco, ...

The draft joint network strategy for the EU until 2028 will be open for public consultation until Nov. 30, 2024. The European Medicines Agency (EMA) and the Heads of Medicines Agency (HMA) announced ...