CRO in Russia - Clinical Excellence Group (CEG)

Clinical Trials Data Management

Medical Writer

Clinical Trial Report

Clinical Trial Protocol

Statistical Analysis

medical device registration

marketing observational research

patient support programs

clineg.com/more-solutions

More Solutions

Registration of Medical Devices.
R&D Strategies development.
Consultations.
Trainings.
Data Management.
Statistical Analysis.
Final Reports on Studies writing.
Journal Articles writing.
Does your company manufacture or promote drugs, cosmetic products, dietary supplements or medical devices?

Have you not been interested in any of the ready-made solutions yet?

Then see what else we offer.

Registration of Medical Devices
We guarantee: Your Company will launch a new medical device to the EAEU market within 11-16 months.
All work stages, from the idea stage to receipt of a Marketing Authorization, will be completed as scheduled.
You will enjoy the quality and reliability of our services and our commitment to results.
Development of R&D Strategies for Novel Drugs and Medical Devices
We have already created 14 such Strategies and provided them to our Customers (IVD medical device manufacturers and pharmaceutical companies).
Each Strategy contains literature review, competitive analysis, program and plan of development and launch, complete set of designs for Non-Clinical Studies and Clinical Trials, detailed descriptions of study protocols, a tentative budget and a project timetable.
Are you also interested in rigorous planning of an innovative project?
Then contact us right now. We will respond within 24 hours.
Consultations
Consultations on development and registration of drugs, medical devices, dietary supplements, and cosmetic products.
Training Courses and Workshops
Training Courses on Good Clinical Practice (GCP) (8- and 42- hour versions).
Training Courses in Data Management and Statistical Analysis (8- and 36- hour versions).
Workshops on Non-Clinical Studies, Clinical Studies, Patient Support Programmes, Russian and the EAEU Legislation on drugs, food supplements, cosmetics and medical devices, Biostatistics, Clinical Epidemiology and Project Management.
In 2015-2018, 63 participants passed the Trainings and obtained CEG Certificates.
Data Management and Statistical Analysis
Plan and implement Statistical Analysis on results of Non-Clinical, Clinical and Non-Interventional Studies.
Medical Writing
Prepare or edit Final Report on biomedical studies and Journal Articles.
What you get when you work with us?
You use our broad expertise and individual approach to your tasks.
See why CEG really can offer you optimal solutions.

Contact Us

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