Regulatory Affairs Support in Europe and CIS

Local Regulatory Affairs Representation

Biomapas provides local regulatory affairs support to clients in both pre-authorization and post-authorization regulatory affairs across Europe and CIS countries. Our full range Regulatory Affairs solutions are dedicated to delivering the highest quality support, assistance and regulatory approvals for our clients utilizing fast, efficient, and cost-effective working practices. Currently, Biomapas is expanding, therefore in a short term we will be able to support you with global solutions, including Latin America, MENA, and Asia. 

Experience

We have assisted our clients in obtaining over 150 Marketing Authorizations via National Procedures in Europe and CIS regions. During the past few years we have performed more than 1000 regulatory submissions. We were/are involved in more than 25 Marketing Authorization Procedures of Medicinal Products via Centralized, Decentralized or Mutual Recognition Procedures. Full Biomapas expertise listed here.

Geographical Coverage

The detailed list of our geographical coverage is presented below (office locations are underlined):

 Europe

Albania Estonia Lithuania Portugal
Austria Finland Luxembourg Romania
Belgium France Macedonia Serbia
Bosnia and Herzegovina Germany Malta Slovakia
Bulgaria Greece Moldova Slovenia
Croatia Hungary Montenegro Spain
Cyprus Italy Netherlands Sweden
Czech Republic Kosovo Norway Switzerland
Denmark Latvia Poland Turkey

CIS Region

 Armenia Georgia  Mongolia  Turkmenistan
 Azerbaijan  Kazakhstan  Russia  Ukraine
 Belarus  Kyrgyzstan  Tajikistan  Uzbekistan

 

For any inquiry regarding our services, please contact Biomapas Business Development team.

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