India is fast emerging as one of the most strategic locations for global pharmaceutical companies to conduct their drug research and development. For studies in many therapeutic areas, the Indian sub-continent is desirable because of its large population of qualified patients, lower trial costs, use of English as the primary language, and a well-trained medical community.
Medwiz is a leading full service Clinical Research Organization that specializes in providing solutions to the twin challenges of speed and cost in clinical drug development.
Medwiz has contacts with leading investigators who excel in their respective Indications/Therapeutic areas. These doctors represent the best and most experienced team of medical professionals throughout India.
Therapeutic knowledge is our foundation and the basis for our bringing together leading experts in their respective fields and assembling dedicated teams with proven experience. We tailor our teams and processes to meet your goals, serving as support pillars to deliver strong science and consistent quality every step of the way.
Anesthesiology | Cardiology | Dermatology | Diagnostics | Endocrinology | ENT |Geriatrics | General Medicine | General Surgery | Gastroenterology | Medical Oncology |Surgical Oncology | Nephrology | Neurology | Neurosurgery | Obstetrics & Gynecology |Ophthalmology | Orthopedics | Pediatrics | Psychiatry | Pulmonology | Rheumatology | Respiratory Medicine | Urology | Vascular Surgery
Our investigators are well versed in the laws and regulations affecting clinical trials in India.
The clinical study teams include:
- Principal Investigators who have proven experience with Clinical Trials, and are specialists in their respective field;
- Medical and non-medical staff to ensure smooth running trials; and
- Social workers that are appointed on trials if needed.
Indian Investigators have proven to be superior in meeting International and Regulatory standards. Indian clinical trial data have been successfully transferred to the US for several FDA approvals.
Our services
- Preclinical
- Protocol Development
- CRF Design and Distribution
- Site Solicitation and Qualification
- Study Monitoring
- Data Capture
- Data and Report Management
- Statistical Analysis
- Report Writing
- Risk Management
- Bioequivalence/Therapeutic Equivalence Studies
