Our consultants have the ability to perform any targeted research and provide a final report to our partners.

The CRENC has well trained and scientifically experienced CRAs and coordinators, all lead by experienced scientists and project managers.

We ensure that all content is run through several softwares to check plagiarism and make sure the content is unique before it is delivered to the clients.

CRENC provides the best educational support to post graduate students, masters, PhD, and clinical researchers.

Our Data Management expertise starts from Protocol Design to Database Lock, following SOPs and Data Management Plans for excellent end results.

We appoint a full-time, highly qualified clinical research coordinator at each study site to assist and support the investigators and site staff with all study related activities.

We help sponsors get quick National Ethics Committee approvals amongst other approvals.

Our clinical monitoring team has thorough knowledge in international GCP guidelines and are proactive in dealing with other research teams.

Our Audit functions in an advisory capacity, providing information, analysis and guidance to research personnel. We make sure it is in compliance with the protocol, the GCP and sponsor’s SOPs.

Our Network Inventory evaluates the feasibility request for a project at a particular site, assisting in timely decision making.

We documentation that will help to achieve their goals. We have proficiency to communicate complex clinical data in a concise and unambiguous manner.

Our translation services are top-notch, done by very proficient professionals with a good mastery of scientific work. Our translated articles meet international publication standards.