Ethitrials is an organization with a broad service foot-print in clinical research and pharmaceutical marketing industry. The company was established in 2011 with a drive to provide quality services in the most ethical way.
With excellent team of the industry experts and consultants with varied experience, we are firmly positioning ourselves as a progressive leader offering large number of services with the aim to become one stop solution for all services required to support client’s R&D and marketing efforts.
To be a leading partner for Pharma and CRO industry for enhancing value to their R&D and marketing efforts.
To help our clients achieve excellence by providing quality services in the most ethical way.
Honesty, respect and courtesy to clients and vendors are the values we enjoy the most.Passion, commitment and accountability are the three most cherished values that help us to follow our mission.
The company is enriched with the collective expertise of over 50 years which ensures quality within the prescribed timeline. Collectively, the team has experience across all stages of development for drugs, devices and biologics with broad range of therapeutic area:
Study designing and conceptualization.Regulatory dossier preparation (Protocol, PIS-ICF, CRF, IB, Patient diaries, study rationale etc.).
Independent auditing and monitoring have become a routine element of quality management. It provides an insight into the quality of your clinical research.
CME modules, Slide kit preparation, Product monograph, Scientific compendium, Leave behind literature,Visual aids, Therapeutic rationale.
In addition to the qualification and basic training, continuous training is recognized to maintain, upgrade and update skills Continuous training is essential.
Whether it is for compliance reasons or to better utilize the space in your office, Ethitrials can access, evaluate, move, store, archive and index your information.
Health policy researchers, conduct research, generate reports, and administer health care policies and programs.
Dr. Bhaumik Mody is a medical professional with post-graduation in Clinical Research and Regulatory Affairs. He has a decade of experience with reputed pharmaceutical companies and CROs like Sun Pharma, Cadila Pharma, LAMDA, Synchron and GVK. During his industry association, he has achieved substantial experience in Phase I-IV clinical trials, BA/BE studies, PK/PD studies and managing clinical supplies distribution. He has managed large teams comprised of medical writing, CRA, data management, pharmacy professionals.
Charmin is an experienced clinical research professional with an edge over the Quality Assurance. After graduation from science stream, he did his post-graduation in Organic Chemistry from Gujarat University. In order to get into the depth of the subject and achieve excellence, he also pursued post-graduation in clinical research after his industry association.
Dr. Deepak Patil is a medical professional with clinical experience as a general physician before assuming the role of medical advisor at Sun Pharmaceuticals. Through his expertise in medico-marketing, he has been able to integrate his prior roles to achieve successful launch of several new products in the fields of Urology and Infertility medicine. Currently furthering his skill set at the esteemed Boston University, USA, he will now include healthcare information systems and management to his profile in the coming months.
50+
Happy Clients
200+
Completed Projects
Commitment
Fast Support
For any business related queries, please contact us on services@ethitrials.com