Clinical Research Services

Reliable and Efficient
Clinical Research Solutions for Every Phase.

Aizant offers clinical research services, which are designed to meet the various demands of the pharmaceutical and biotechnology industries from early stage to late phase clinical trials for drug and device development programs for various therapeutic areas.

With a commitment to quality and regulatory compliance, we have conducted more than 1200 clinical studies under good clinical practices (GCP), maintaining the highest standards of integrity and ethics in every trial.

Bioavailability and Bioequivalence (BA/BE)

We provide BA/BE services, which support regulatory compliance and fast-track approval for generics and new formulations. Our expertise combines scientific knowledge and regulatory insight to accelerate market entry.

Bioanalytical Services

Our bioanalytical services support the development of Generics, Complex Generics, New Chemical Entities (NCEs), New Drug Applications (NDAs), and Clinical Trials with over 500 validated methods. Using advanced technology like LC-MS/MS and ICP-MS, we deliver precise, regulatory-compliant testing.

Clinical Trials

We specialize in clinical trials across all phases (I-IV), offering comprehensive trial management services. From protocol development to volunteer recruitment and data collection, our expert team ensures global regulatory compliance and flexible support tailored to your needs.

State-of-the-Art Facility and Infrastructure

2 Clinical Units

A combined capacity of 190 beds, capable of handling diverse studies simultaneously.

60,000 Sq. Ft. Facility

Dedicated space with UNIFLOW direction for streamlined workflow, by maintaining safety, compliance, and efficiency.

In-House Diagnostics

Offering real-time analysis and monitoring throughout your study to enhance data accuracy and minimize delays.

IEC/IRB Access

Upholding the highest ethical standards through an Independent Ethics Committee (IEC) and Institutional Review Board (IRB).

2 Hospital Partnerships

Strategic partnerships with nearby hospitals (within 10 minutes) for quick access to medical support.

Global Regulatory Accreditations

Certified by leading regulatory bodies, securing global compliance for clinical trials and drug development.

Healthy Volunteer Pool: 40,000+

Male Volunteers

Access to a diverse database of 35,000+ male volunteers.

Female Volunteers

4,000+ female volunteers, including a dedicated pool of post-menopausal women, providing a broad spectrum of participants for clinical trials.

Automated Data Management

Utilizing VCPMS, an automated clinical data management system, combined with advanced biostatistics, providing accurate, real-time data analysis to support regulatory submission requirements.

  • Efficient data collection
  • Real-time insights
  • Regulatory compliance
  • Data integrity
  • Scalable & flexible

Start your clinical development journey with us get in touch with our experts today!