Welcome to MENA Clinical Research

MCR is a Leading Contract Research Organization that provides Clinical Trials Management Services in MENA region. Our unique region coverage and highly experienced team will assure your smooth and fast study start with high quality deliverables during the study conduct. 
In this very advanced and complicated regulatory environment, there is an enormous need for a successful partnership between sponsors and health care providers. Together we can build this highly regulated environment where patient health is our primary interest.



Global Health Starts Locally

Our Advantages

Why MENA Clinical Research

Local Expertise Across the Region 

At MCR, our main goal is to provide the local market with a well trained expertise across MENA. Our experts are highly qualified with academic knowledge and  experience that can deliver the critical solutions and smooth conduct to your studies, with consistence quality deliverables, customer support and sustainable solutions.

Sites and Patients Solutions 

Our relation with study sites allows better and fast site selection process based on study site experience and previous enrolment figures.  

Our Presence Across MENA

Our team is highly qualified and experienced with consistence quality deliverables, customer support and sustainable solutions. 

Our Services

Feasibility and Site Selection

Our experienced staff helps in selecting the best sites to perform your clinical trial, our investigator database will allow selecting the best investigators who are experienced in conducting clinical research, as well as selecting the best sites that is experienced in conducting quality clinical trials with best patient access. 

Regulatory Submission

o Our experienced start-up team will prepare study submission packages and perform initial submissions and subsequent follow up for your study starting from local Ethics Committee (EC) ending with country Regulatory Authority (RA)
o Our team will successfully engage in contract negotiation with sites and investigators  

Project Management and site Monitoring

At MENA Clinical Research, we assure fast site readiness and preparation for site initiation, our experienced CRAs will be responsible for performing site training (initiation visit) to the investigative site and will assure site readiness for patient recruitment.

Real World and Late Phase 

As Regulators and biopharma are increasingly demanding more data about the new marketed products, we here help our clients to bridging between the clinical research data and the market.

Medical Writing, Data Management and Statistical Analysis.

Training

Are you interested in clinical research? Are you planning to advance your career as a clinical research professional? What do you know about GCP and clinical research regulation?

Therapeutic Experience

MCR developed its clinical experience through all clinical trial phases in the following therapeutic areas across MENA region: 

Hematology/Oncology  
Cardiology 
Endocrinology/Metabolism
Respiratory 
Infectious disease 
Rheumatology 
Urology 
CNS

Our Presence 

Quick links to regulatory authorities

Jordan

http://www.jfda.jo/

Jordan is among the most important potential markets for clinical trials in MENA, where all clinical trials are fully regulated by Jordan Food and Drug Administration (JFDA). 
Jordan is characterized by a well developed health-care system with highly experienced physicians and medical staff as well as well equipped hospitals that are capable of conducting all types of clinical trials. 

Saudi Arabia 

https://www.sfda.gov.sa/

Saudi Arabia is characterized by its highest population and recognized as largest pharmaceutical market among Gulf countries. All Clinical trials in the Kingdom are regulated by Saudi Food and Drug Administration (SFDA). Kingdome is characterized by highly regulated, experienced and very well equipped sites with specialized units to facilitate the conduct of clinical studies.

Egypt

http://www.mohp.gov.eg/default.aspx

Being the country of the largest population in MENA region, Egypt is one of the main countries to conduct clinical trials. With highly experienced physicians and medical staff as well as high research experience in most of the therapeutic areas, Egypt is considered to be the best place to conduct your trial. 

Lebanon

https://www.moph.gov.lb/en/Pages/0/10483/clinical-trial-regulations

Lebanon is considered to be a pioneer in conducting clinical research in the region, that was selected for participation in vast number of international clinical studies. It is characterized by a highly experienced investigators and site staff in about 22 university hospitals in Lebanon some of which are affiliated to major European and American hospitals.

Gulf States 

At MCR we will support your study in Gulf countries including; Dubai, Qatar, Kuwait, Oman and Bahrain. 

Palestine Territory 

MCR can offer your clinical research study coordinators and clinical research associates within Palestine territory. We are your best choice if you still searching new areas within MENA region with excellent patient naïve population and highly educated physicians and study team.