We bring a high level of expertise and high value technology to every clinical trial. Factors of prime importance to us are to Provide Quality Solutions, Reduce Costs and to Accelerate Timeliness.
Preclinical
Regulatory submission
Phase of I,II,III and IV BA/BE studies
Pharmacovigilence - SAE reporting
Medical Writing
Expertise in overall execution of Clinical Trial from protocol preparation, site selection, monitoring & auditing of the
trial
to data management & final report submission for:
Cardiology
Gynecology & Obstetrics
Orthopedics
Dermatology
Nephrology
Pulmonology
Endocrinology
Neurology
Rheumatology
ENT
Oncology
Gastroenterology
Ophthalmology
Over 560 research centers and hospitals nationwide
Nearly 620 investigators and good "Population Data" from various therapeutic areas
Investigative sites are located in more than 30 cities across India
Factors that Continue to Make India Attractive for Future Clinical Trial Outsourcing:
Increasing Global R & D Costs across the board
Increasing Pharmaceutical Development Time
R&D costs in India are substantially less than those in the developed world
India has a large, heterogeneous population pool
World Class Facilities
Patent Protection and Intellectual Property Rights
India possesses a world class data-processing
India possesses large generic drug manufacturing facilities
