
Pfizer has pulled out of a $195 million deal with UK firm Biotica, as it continues to downsize its global …
Wainwright Associates is an independent company offering consultancy services to the pharmaceutical, medical device and healthcare industry in Product Development, …
The first 75 ‘pathfinders’ have been named in Local HealthWatch, the patient representative organisations due to replace the current local …

NICE has not recommended Novartis’ multiple sclerosis drug Gilenya because of its cost and ‘uncertainties over its clinical effectiveness’. Gilenya …
Roche’s personalised asthma drug lebrikizumab has met its primary end point in a phase II trial. Lebrikizumab increased the level …
The government is highlighting a scheme in West Yorkshire as providing a way forward for reducing the cost burden on …
Big pharma’s policy of mergers and swingeing cuts is having a devastating effect on drug research, says a former Pfizer …
With the increasing number of biologics coming to market, the demand for drug delivery solutions such as auto injectors has …

Pfizer looks set to spin-off or sell its animal health and nutrition business units in order to focus on human …
Japanese photography and imaging company Fujifilm has taken another step into the healthcare sector with a new joint venture with …
Actelion’s prospective multiple sclerosis pill ponesimod has cheered the company by meeting its primary endpoint in a phase IIb trial. …
The deal to raise America’s debt ceiling could have long-term consequences for the US pharma industry. The tense stand-off between …
Teva and Active Biotech’s oral MS drug laquinimod has failed to meet its primary endpoint in a phase III trial. …
Vaccines made by Merck & Co at its West Point facility in Philadelphia, US, have been found to be contaminated …
Quintiles is set to launch its first contract sales project in Russia with a 40 strong sales team. The company …
BARCELONA, SPAIN and GERRARDS CROSS, BUCKS, UK – 26 July, 2011 – Veeva Systems announced today that Daiichi Sankyo, one …

For the past decade prolongation of the QT interval has been used by the regulatory agencies as the principal biomarker …
European regulators have recommended the approval of a new, once-daily form of Boehringer Ingelheim’s HIV treatment Viramune. Viramune (nevirapine) has …

The FDA has refused to file Eisai’s epilepsy drug perampanel, saying it needs more information for the treatment. The FDA …
Udit Batra is to join Merck KGaA as head of its consumer health care division on 1 September. He moves …