News

The European Union's efforts in combating rare diseases reached a new milestone this October, with the 50th positive opinion on an 'orphan' medicine being adopted by the EMEA's Committee for Medicinal Products for Human Use (CHMP).

Patheon, a global provider of drug development and manufacturing services to the international pharmaceutical industry, today announced the opening of its new headquarters for its European operations in Zug, Switzerland, near Zurich.

DIA Forum

Drug Information Association (DIA) is conducting an event called European Regulatory Affairs Forum which will be held from 24th November 2008 in Munich, Germany.

Nextrials? Prism wins gold in the mobile star awards for health care data capture technology.

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The Foundation for Improving Data Quality (FIDQ) advances the evaluation of clinical trial methodologies that aim to improve the clinical integrity and reliability of clinical data.

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A Global Regulatory GPS?

Finding a global regulatory GPS of ethics committee and competent authority approvals.

ECRFPlus achieves milestone multimillion dollar enterprise agreement with CRO and launches e-CRF+(TM): a CTMS and EDC Web platform with ECG analysis and cardiac safety module.