News

India: new strategy to boost pharma exports

India has announced plans for a new short-term strategy aimed at boosting pharmaceutical exports, and has also set guidelines for domestic drugmakers to comply with a European Union (EU) directive on imports of bulk drugs into Europe.

Non-Hodgkin’s lymphoma survival rates double in England

Twice as many patients with non-Hodgkin’s lymphoma (NHL) are hitting a post-diagnosis survival marker than in the 1970’s, a report by Cancer Research and the Haematological Malignancy Research Network has found.  

Tufts report sees growing use of adaptive trial designs

Around 20% of clinical trials currently underway are using adaptive designs, while adoption of these techniques is likely to increase significantly over the next few years, particularly in the exploratory phase of drug development, a new report suggests.

J&J sees 10 new products by 2017

Johnson & Johnson says it is looking to have ten new pharma products on the market in the next four years as it looks to build on a strong 2012.

ACRO joins Coalition of Small Business Innovators

The US-based Association of Clinical Research Organizations (ACRO) has joined national grouping the Coalition of Small Business Innovators (CSBI), citing the need to ensure funding for emerging research-intensive companies in the biopharmaceutical and medical device sectors.

Boehringer in bother with FDA over manufacturing

Boehringer Ingelheim says it will act promptly to resolve a series of manufacturing complaints highlighted by regulators in the USA concerning violations at its German headquarters.

ClinTec to open office in Istanbul

UK-based contract research organisation (CRO) ClinTec International will formally open an office in Istanbul, Turkey as the company further consolidates its strong presence in the Middle East and North Africa (MENA) region.

Elan rejects higher bid from Royalty

Irish drugmaker Elan has once again spurned the advances on Royalty Pharma, despite the latter having upped its bid to $12.50 a share, or around $6.4 billion.

FDA panel backs Merck & Co sleep drug but at low doses

A panel of experts at the US Food and Drug Administration has recommended Merck & Co’s insomnia drug suvorexant when given in lower dosages but rejected the higher dose that the company was seeking.