EMA recommended 17 drugs for marketing authorization in December, including treatments for rare heart conditions, anemia, and liver disease.

The Center for Drug Evaluation and Research’s new center will coordinate and promote use of real-word data in regulatory ...

AbbVie has completed its acquisition of Aliada Therapeutics which includes Aliada’s disease-modifying therapy for Alzheimer’s ...

This paper explores the legal and regulatory framework around 3D drug printing, particularly for personalized medicine, ...

With so many personnel involved in the development and manufacture of pharmaceuticals, proper training of all staff is key to ...

A statistical procedure based on a quality range is proposed for demonstrating comparability between pre-change and ...

The European Commission has developed a roadmap aimed at reversing the rising trend of cancer across the European Union.

Edwin Stone, Bernard Sagaert, and Khaled Yamout go behind the headlines to discuss what the ongoing measles outbreak in the ...

Colin McKinlay, the senior director of Chemistry and Delivery Technologies at Nutcracker Therapeutics, discusses current challenges in mRNA and LNP manufacturing as well as innovations that meet these ...

Pharmaceutical Technology® spoke with Nicola Reid, Associate Director Product Management, Endotoxin Products at Charles River ...

All CGMP requirements, including supporting activities, are critical in aseptic sterile manufacturing to ensure product ...

Centogene NV and ROPAD consortium publish data from a landmark study identifying genetic variants that may respond to ...