Bulk ingredients

Exela expands North Carolina facility

Exela expands North Carolina facility

Exela Pharma Sciences will invest $8.5million in its research and manufacturing plant in North Carolina. The venture, to be spread over the next three years, will provide 38 new jobs almost doubling its present workforce. 

Questcor buys API maker Biovectra

Questcor buys API maker Biovectra

By Gareth Macdonald

API maker BioVectra has been acquired by autoimmune disease focused drugmaker Questcor Pharmaceuticals for C$50m.

BASF wont extend Pronova offer again

BASF wont extend Pronova offer again

By Gareth Macdonald

BASF says it will not extend its offer for pharmaceutical-grade omega-3 supplier Pronova BioPharma ASA beyond new mid-January deadline.

Aesica says academic partnerships are key for CMOs

News from CPhI

Aesica says academic partnerships are key for CMOs

By Gareth Macdonald

UK CMO Aesica Pharmaceutical says that working with academia to access cutting edge technologies is critical for contractors that want to meet the demands of the modern drug industry.

Manufacturing deals for DSM, Lonza, ARk and AMRI

News from Lonza, DSM, Ark and AMRI

Outsourcing-pharma.com presents a roundup of contract manufacturing news with deals for Lonza, DSM and Ark Therapeutics and an expanded agreement with Shire for AMRI.  

Fluid bed processing equipment at the Wittenburg site

SternMaid pumps cash into fluid bed processing

By Rod Addy

SternMaid has invested €14m in its Wittenburg factory to enlarge capacity and extend the range of its products and services, involving the introduction of new fluid bed technology.

Scottish life sciences sector grows

Scotland's pharma services sector grows with Govt support

By Gareth Macdonald

Scotland’s emergence as a biopharma hub – as evidenced by announcements by SAFC and Quintiles last week – is due to Government support, electronic health records and speedy trial approvals says Scottish Enterprise.

FDA warning for DPT Labs

update

FDA criticizes DPT's efforts to fix sterility problems

By Gareth Macdonald

US CDMO DPT Labs has not done enough to investigate sterility failures observed during a March inspection according to the Food and Drug Administration (FDA) which wants a ‘comprehensive evaluation’ of sterile drug operations.