• State-of-the-art 22,000 square feet air-conditioned facility text

• Extensive volunteer database of 33,000 male and female subjects.

• NABL-accredited bar-coded Central lab on-site for study subject screening.

• Air-conditioned facility with well-designed 1 CPUs having a required beds for simultaneous mixed population studies.

• OVIS software implementation to prevent cross-participation.

• Fool-proof server connected with ECG machines for precise data recording.

• Volunteer Housing & Dosing: Safe, controlled housing for volunteers during dosing and study procedures.

• Dosing & Investigational Product Administration: Precise administration of investigational drugs with continuous monitoring.

• Clinical Trial Management: Full management of study operations including recruitment, dosing schedules, and randomization.

• Pharmacy Services: Safe handling, preparation, and administration of investigational products.

• Sample Storage & Archival: Secure storage of clinical samples ensuring traceability and data integrity.

• Regulatory Compliance: Adherence to FDA, EMA, and ICH guidelines for thorough documentation and inspection readiness.

• Informed Consent & Ethics: Ethical conduct and robust informed consent process ensuring transparency and safety for volunteers.

• 24/7 power backup and emergency management with in-house ambulance services.

Our Bioanalytical Services support every phase of clinical development, ensuring precise and reliable data to advance your research. We offer a comprehensive range of bioanalytical testing services designed to meet regulatory standards and provide critical insights into drug development.

• Bio-analytical Lab equipped with LC-MS/MS instruments for efficient sample analysis.