The Clinical Research Network India (CRN India) is a nationwide consortium of experienced clinicians, expert researchers and clinical research sites with common goal of providing the infrastructure to support to high quality level clinical research and studies to accelerate the development of life-saving drugs and devices that save lives and improve quality of life. CRN India is one of the largest alliances of practicing clinicians graduated from Premier medical school i.e. AIIMS, PGI, MAMC, KGMC, SGPGI, IPGMER, SRMC, KLE’s JNMC and many other institutions. All of our investigators are board and GCP certified and ensure CRN India is set to meet or exceed industry standards.
With over 100 sites in 29 states, CRN India is one of the largest growing alliances of clinical trial research sites in the country. The integrated resources of CRN India provide unique advantages for conducting clinical research in India. Our goal is to provide a comprehensive solution to conducting clinical research in India, from start to finish.
Mission:- To provideis highest levels of excellence and quality service with passion, knowledge and integrity.
Vision:- To MAKE INDIA as a World leader in ethical clinical research.
Goal:- To provide Healthy life to every individual through translational research
Clinical research network India (CRN India) is a research network founded in 2015 to provide a comprehensive solution to potential hurdles associated with conducting clinical research in India.
The network partners with researchers/clinicians, primary care physicians, contract research organizations, site management organizations, the Government, health associations, not for profit organizations, biopharmaceutical and medical device companies as well as the patients and public.
Our purpose is to provide the critical link between policy makers, researchers, health caregiver, and the beneficiaries (patient/public) in health care delivery settings.Read More
Medicinal Service Company puts stock in conveying the most elevated quality administration with quality and sympathy every day.
Choose from our wide database of experienced investigators network specialized in diverse core therapeutic areas.
We firmly believe that accurate initial feasibility assessment is a key factor in the success of a study with on-time enrolment.
Our regulatory staff coordinates with sites and local ECs for approvals of clinical studies, including submission, query resolution and follow up.
Subject safety is foremost in clinical research while meeting the actcrual goals. Our staff is trained to navigate these twin goals.
We will match our in- house expertise and personnel specifically to each project to streamline the writing process.
Our team of highly disciplined and ethical writers will ensure that your intellectual property is kept in utmost secrecy.
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