Registration of medicines and medical equipment: How effective collaboration between manufacturer and consulting company helps save time and money
In December 2016, the company RegMed Prof will participate in the APTEKA exhibition for the third time.
The company has been operating on the consulting market in the sphere of state regulation of medical products for more than 15 years. Years of successful work have been made possible thanks to the tireless and conscientious work of the whole team, its ability to respond quickly to changes in legislation, competent work with partners, building long-term and trusted relationships with peer organisations and testing centres.
At the exhibition we will present not only information about our services, but also a unique informational project — an overview of Russian legislation in the context of registration and civil circulation of medicinal preparations. One brochure, in plain language, with reference to the relevant laws, orders and guidelines, will describe in detail the process of registration, the pitfalls, and also the requirements for documentation, special aspects in the registration of certain categories of medicines, and clarification of some ambiguous provisions of FZ-61. Particular attention will be paid to clinical trials for the purpose of registration in the Russian Federation, their volume and specifics. The materials will be presented in Russian and English languages.
See you at APTEKA 2016.
Director General of RegMed Prof,