National Marketing Authorization Applications

Decentralised, Mutual Recognition, National Procedures

We have assisted in obtaining over 150 Marketing Authorisations via National procedure in Europe and CIS regions. We were/are involved in more than 25 Marketing Authorisation procedures of medicinal products via Centralised, Decentralised or Mutual Recognition procedures.

We provide full-scope service of procedure management, starting from the booking of a slot for Decentralised or Mutual Recognition procedures, dossier development, pre-submission assessment, eCTD compilation and submission to competent authorities, support in preparing responses to deficiencies reported by the Competent authorities, full support during CHMP and CMDh referral procedures, until the granting of Marketing Authorization.

Big Enough To Cover  All Your Needs. Small Enough To Care.

Discover the tailored solutions that Biomapas provides to accelerate your clinical trials and optimize your drug development process.

Clinical Research

Regulatory Affairs

Pharmacovigilance

Medical Information

Big Enough To Cover All Your Needs.
Small Enough To Care.

Discover how Biomapas provides all the support to accelerate your clinical trials and optimize your drug development process.

Clinical Research

Reliable support for every phase of your clinical trial, from recruitment to results.

Pharmacovigilance

Flexible safety monitoring to keep your products compliant and trusted.

Regulatory Affairs

Confidently navigate regulatory challenges with expert support.

Medical Information

Clear, accurate medical information 24/7, tailored for global audiences.

Quality Assurance

Export auditors help identify gaps and close them with actionable solutions.