Transparency Push: EMA to Revise Policy on Document Access

The European Medicines Agency (EMA) on Friday proposed a revision to its policy on accessing documents, extending the scope to include corporate documents, and increasing the publication of clinical data for pharmaceuticals. Since October 2016, EMA has published pharmaceutical trial data via its new website, including for: Mylan’s aripiprazole, published most recently on 31 January 2017,…

$74M to be invested in Azerbaijan’s first medicine plant

The Azerbaijani-Russian joint pharmaceutical plant will come to full production capacity in 2020, said Azerbaijan’s Economy Minister Shahin Mustafayev. He made the remarks Nov. 2 during the plant’s groundbreaking ceremony in the Pirallahi Industrial Park. This is Azerbaijan’s first pharmaceutical plant, said the minister, adding that a 10-percent share in the joint venture will be…

Kazakhstan and Hungary signed memorandum on expansion of pharmaceutical production

Within the framework of the Kazakh-Hungarian business forum the «Kaznex Invest» JSC, the JSC “International Research and Production Holding “Phytochemistry” and Hungarian company «PannonPharma LTD» signed a memorandum of understanding on organization and expansion of the production of original medicinal drugs based on plant matter in Karaganda. “Today we produce about 2 million ampules, about…

Global Pharmaceutical Regulatory Affairs Summit

Informa Life Sciences’ Global Pharmaceutical Regulatory Affairs Summit, taking place on 27th – 29th October 2015 in Berlin, Germany, combines two previously separate events, ‘Regulatory Affairs in Emerging Markets’ and ‘Global eSubmissions’ to bring you increased networking and 3 highly focussed streams. Stream 1: Regulatory Affairs in Russia, CIS, Turkey and MENA Stream 2: Regulatory…