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EMEA pharmaceutical news in briefs.

THE EUROPEAN Medicines Agency (EMEA) has released a guideline on developing, producing, characterising and specifying monoclonal antibodies and related products --;

* EMEA has also released a draft policy on obtaining practical access to its documents--;

* This includes a document on accessing its adverse reactions database EudraVigilance-- pdfs/human/phv/18743906en.pdf.

Other recent EMEA documents include a guideline on the clinical development of medicinal products for the treatment of HIV infection

(; and developing specific immunotherapy products treating allergic diseases

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Author:Nuthall, Keith
Publication:International News
Date:Jan 1, 2009
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