Healthcare data services firm Exco InTouch has appointed Laurence Burke as its vice president of Operations. Burke takes over 20 …

A key adviser to the European regulator has said that Gilead Sciences’ fixed-dose combination of Sovaldi and ledipasvir can be …

Simon Sturge is joining Merck KGaA from Boehringer Ingelheim in order to head its Biosimilars unit. In his new role …

The CHMP has given its backing to GlaxoSmithKline and partner Theravance’s new chronic obstructive pulmonary disease medicine Anoro. The treatment …

Drug development firm Avillion has appointed Dr Allison Jeynes-Ellis to be its chief executive. By stepping into the role Jeynes-Ellis …

Novartis is celebrating after its investigational pill targeting the most common form of skin cancer met its primary endpoint in …
Authorities in Japan have raided the premises of Novartis’ Tokyo operation as part of an ongoing investigation into the promotion …

A recently-published Apple patent has shed light on a new health-monitoring device that will be built into a pair of …

Life sciences executive search and interim management firm RSA has appointed Claes Zackrisson as its first director of information. Zackrisson …

French firms Servier and small biopharma cancer specialist Cellectis have signed a deal to develop and commercialise one drug targeting …

Boehringer Ingelheim attempted to delay and revise the publication of important drug information surrounding its new anticoagulant Pradaxa. This is …

Regulators have shown the green light to BioMarin Pharmaceutical’s Vimizim as a treatment for a rare enzyme deficiency which affects …
The giant NHS database that could allow pharma firms to buy into patient records will now not be launched until …

The European Medicines Agency (EMA) has welcomed Dina Tsiambaou as the new head of its Information Technology department. Tsiambaou joins …

The rumours of a substantial deal for Forest have been proven true after Actavis announced this afternoon that it will …

Bayer HealthCare has expressed its dismay after the Food and Drug Administration once again rejected further indications for the company’s …

An internal review of the US Food and Drug Administration has concluded that the agency needs to restructure its compliance …

GlaxoSmithKline has begun a Phase III study to look at mepolizumab in a rare condition characterised by vasculitis – widespread …