About Us

Empowering Clinical Research Through Expertise & Integrity

We understand that navigating clinical research can be complex

Nexus Pharma Group delivers seamless support across the clinical study lifecycle, combining industry knowledge, strong regulatory understanding, and a quality-first approach. We partner closely with sponsors and sites to ensure every study is conducted with precision, integrity, and full regulatory alignment.

Years of combined experience in clinical research & regulatory operations

Studies, submissions, and projects supported across diverse therapeutic areas

Client satisfaction rate for our quality, communication, and on-time delivery

Our Values

Quality
We uphold the highest standards across all processes, from start-up to close-out.
Compliance
Our work adheres to ICH-GCP, national regulations, and global ethical guidelines.
Innovation
We continuously refine our systems, tools, and workflow to enhance efficiency and accuracy.

To deliver world-class clinical research services rooted in scientific excellence, operational precision, and ethical responsibility — ensuring every study is conducted with the highest level of quality and compliance.

To be the leading partner in clinical research, recognized for our commitment to advancing medical science through innovative solutions and unwavering integrity.

What Makes Us Different

We deliver high-quality solutions backed by deep expertise and strong integrity. Our team ensures every project is handled with precision, clear communication, and a commitment to achieving reliable, impactful results.

Global ICH-GCP Compliance
Every process is aligned with international regulatory standards.
Experienced Clinical Teams
Skilled CRAs, PMs, and regulatory experts at every stage.
Audit & Inspection Readiness
Meticulous documentation and proactive oversight.
Quality-Driven Monitoring
Ensuring reliable data and participant safety.
End-to-End Operational Support
From feasibility to close-out, we manage the entire lifecycle.

How We Deliver Results

A step-by-step framework built to enhance quality, minimize delays, and support evidence-driven clinical progress.

Global ICH-GCP Compliance

Every process is aligned with international regulatory standards.

Regulatory Preparation

We manage all ethics, governance, and regulatory submissions to ensure smooth and timely approvals.

Monitoring & Reporting

We oversee study progress, ensure data accuracy and protocol compliance, and deliver complete, regulatory-ready final reports.

Site Activation

We select qualified sites, finalize contracts, train investigators, and activate sites efficiently for study launch.

Meet Our Experts

A highly skilled team committed to quality, compliance, and exceptional service

Dr Kapil Vithani

Compelling Biography