Clover Euro Medica

We are Your strategic partner to access the European Market

European Based Research Organization located in heart of Brussels and the Center of Europe, operating under the Guidance of Key European and International Thought Leaders.

We provide a wide range of consulting services to foreign medical device manufacturers aiming to reach farther into the European market.

Cloverem members have acquired over 20 years of deeply-rooted expertise in Clinical and regulatory affairs in a broad spectrum of medical fields and therapeutics area.

Our main strategic and operational services are:
 Guidance and Strategy advices on Clinical Development and Regulatory
 Negotiation with Notified Body
 Assistance in CE mark filing till approval
 Drafting Clinical Evaluation Reports (CER) and annual update
 Conducting clinical trials and Providing a full range of clinical services
 Full service Post Marketing Clinical Follow-up PMCF
 Link between industry and regulatory authorities as well as health technology institutions
 Developing KOL network
 Product registration in different EU countries as well as
Brazil, India, Israel and Turkey etc. who recognizes CE marking

Company’s Keywords:

clinical affairs, research studies, reports, regulatory affairs