News

Environment Committee adopts Willmott amendments to CT regulation

The European Parliament’s Committee on Environment and Public Health has unanimously adopted rapporteur Glenis Willmott’s amendments to the Commission’s proposed regulation on clinical trials, including provisions requiring sponsors to publish full Clinical Study Reports once a marketing-authorisation decision has been taken.

Ireland passes reference pricing, pro-generics law

Legislation to enable the introduction of reference pricing and pro-generic initiatives has now been passed by both houses of Ireland’s parliament (Oireachtas) and is expected to take effect next month.

NICE: GPs need to do more to get patients moving

Under its expanded health and social care remit, NICE has released new advice to GPs and practice nurses to help them identify adults who are not active enough and to encourage them to get moving.

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.