The first session “Maintenance of drug production and quality assurance organization in compliance with the cGMP” held on 4-12 December 2006.
The Non Commercial Partnership “Center of Modern Medical Technologies” TEMPO organized the session with support from BioIndustry Initiative Program (BII) and CRDF.
The leading Russian and American experts in the field of drug bioprocessing and production attended. The practical demonstrative studies were conducted on the base of the Scientific-Production Union “PetrovaxFarm”, that works in strong compliance with GMP standards and proceedings.
30 specialists from TEMPO members-organizations were trained.