Considering the Government Act no. 1714 ddt from the 26th May 2016, any registration of API/AVI or FDF product either for medical or veterinary use in Russia requires a GMP certificate issued by the Ministry of Trade and Industry of Russian Federation.
Our specialists have a wealth long-term experience in leading pharmaceutical companies, they have undergone specialized training, thus letting "PROTEK-SVM" implement comprehensive assessment of every particular manufacturing site with revealing of all discrepancies, their classification as per degree of significance and further working out of corrective actions provided to you by our team (if any are needed).
In order to secure sucesfull GMP audit of your manufacturing site we are offering you a full pre-inspection procedure and consultation support within context of GMP certification.
For further details on terms and pricing please contact our specialists: .+7 (495) 231-28-61, ext..28-15 or e-mail KA_LUSHOV@protek.ru
GMP certificate indictaes that the products are manufactured in a strict complience with conditions that do not allow contamination or any foreign materials ingress, and packed in a manner that preserves their performance and quality.