Our comprehensive services covered
from protocol development to final study reports,
and are in compliance with ICH-GCP, ISO/IEC 17025 and
GLP requirements.
• Protocol Development
• Regulatory Approval
• Ethics Committee Approval
• Study Population
• Clinical Study
• Analytical Method Development & Validation
• Bioanalysis
• Data Management & Statistics
• Report writing & Submission
• Quality Assurance
Our modern in-house 30 beds are available for early
clinical trials, bioavailability and bioequivalence
studies with special care and treatment from our well-trained
medical professionals. We serve our clients with state-of-the-art
clinical research facilities with adequate recreation,
dining and entertaining functions for volunteers.
• Total 30 beds (male and female separartion)
• One ICU
• Pharmacy to store study drugs (Access controlled)
• Screening room
• Sample preparation room
• Changing room
• Life saving equipments and drugs
• Synchoronized clocks all over the company
• Modern facility with dining and entertaining
functions
• Computers with internet access
• TV + DVD
• Book, Magazines, Puzzles, Card games etc.