MDA -Medical Development Agency

Clinical Research Organization – medicine registration, clinical trials, market access in Russia

Medical writing
GMP inspection
Clinical trials
Pharmaceutical Regulatory Affairs
Post approval research
Market access
Bioequivalence
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MDA-CRO in Russia
MDA-CRO in Russia
Our main areas of activities - regulatory affairs procedures in Russia consultancy, organizing and conducting pre-clinical and clinical trials, post approval research, post marketing studies, phase IV trials and patient registries, bioequivalence trials, consulting services on pharmacovigilance, medicine registration for pharmaceuticals in Russia, and a variety of medical and social projects.
Our team
Our team
Medical Development Agency employees are not just experienced professionals with a solid background of knowledge, skills and successfully implemented projects. We are a friendly, close-knit team that ensures a high level of efficiency of our work and the company's competitiveness in the market.
Our  achievements
Our achievements
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Registrations
0
Market analysis
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Clients

About our company

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Medical Development Agency (MDA)

Contract Research Organization (CRO) Medical Development Agency has been operating in Russia since 2011. Our main areas of activities - regulatory affairs procedures in Russia consultancy, organizing and conducting pre-clinical and clinical trials, post approval research, post marketing studies, phase IV trials and patient registries, bioequivalence trials, consulting services on pharmacovigilance, medicine registration, market access for pharmaceuticals in Russia, and a variety of medical and social projects.

Our staff consists of managers with solid knowledge and skills who have successfully completed a vast number of projects. It is also a friendly, close-knit team, contributing high level of efficiency and competitiveness in the market to our company.

High quality services provided by us have been highly appreciated by our clients with leading international and Russian pharmaceutical companies among.  

Medical Development Agency's reputation as a reliable partner is based on strong principles and rules that we strictly follow.

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Why choose us?

Medical Development Agency's reputation as a reliable partner is based on strong principles and rules that we strictly follow.
Professional <br> team
Professional
team
High level<br> of efficiency
High level
of efficiency
100% process<br>control
100% process
control
Awards &<br>Diplomas
Awards &
Diplomas
Conferences & <br>Congresses
Conferences &
Congresses
Quality & <br>Accreditation
Quality &
Accreditation

Our services

List of essential services provided by Medical Development Agency (MDA)
Pharmaceutical Regulatory Affairs in Russia

 

We provide a full range of services for the state registration of medicines in Russia EEU / CIS.

 

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Clinical trials in Russia.

 

Clinical research in Russia is not only a necessary component in any development of new drugs. Clinical trial results, efficacy and safety data should be submitted to regulatory authorities.

 

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Bioequivalence studies in Russia

 

Bioequivalence means that the reconstituted drug active ingredient is absorbed by the body with the same speed and in the same amount as the original product.

 

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GMP inspection

 

Starting from 2016, all pharmaceutical companies must submit a copy of their compliance report when registering new medicines (LP) ...

 

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Market access

 

Specialists and consultants of Medical Development Agency understand the changing national health system environment and can correctly evaluate its impact on your business...

 

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Pharmacovigilance

 

Our Medical Writing Solutions are designed to provide our clients with unmatched expertise, collaborative efficiency, unprecedented quality registration documents and primary manuscripts.

 

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Pharmacoeconomics

 

Medical Development Agency has a broad and deep experience in the field of post-approval studies in Russia, combined with a solid base in the late-stage clinical trials management.

 

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News

News of drug registration and clinical trials

The Board of the Eurasian economic Commission approved The "guidelines for preclinical safety

The state Duma Committee on health protection approved the draft Federal law "on amendments to

On 15 October, the Committee of the European Directorate for quality of medical products (EDQM)

According to the analytical Agency DSM Group, the volume of the Russian commercial LP market in

Contact us

121096, Russia, Moscow,
Vasilisy Kozhinoi str., office 803.6
+7 (495) 74-88-777
info@mda-cro.com
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