Our deep knowledge of the regulatory environment and legislation ensures successful submissions and approvals.

We support marketing authorizations throughout the product lifecycle keeping close collaboration with related functions such as pharmacovigilance and quality assurance.

(NOVA EastPharm provides professional regulatory services on registration (marketing authorization) of medicienes and certification and medical devices and equipment across Ukraine and CIS countries. The specialists of our company provide support for all registration processes, starting with the registration or certification of products and continuing with subsequent supporting all post-registration and post-certification processes for products on the market.)