CRO – Boston International Clini School

Where Medical Expertise Meets Global Clinical Research

Backed by a medical advisory team with 60+ years of trial oversight, BICS delivers full-spectrum CRO services—from Phase I to PV—with a zero-critical-finding track record and dual-site delivery advantage.

Why Sponsors Trust BICS

At Boston International Clini School (BICS), we don’t just offer services — we become your strategic partner in compliant, efficient, and medically-supervised clinical research.

Zero-Critical Audit Record

Over 50 clinical and pharmacovigilance inspections passed since 2019 with no critical findings. Every process is governed by ICH-GCP–aligned SOPs and quality assurance protocols.

Clinician-Led Oversight

All studies at BICS are medically supervised by MBBS/MD professionals with 25+ years of experience. Our senior investigators bring real-world hospital expertise, ensuring protocols are both scientifically sound and ethically grounded.

India + Dubai Trial Network

Sponsors gain access to patient pools and regulatory frameworks across two strategic clinical geographies—India and the UAE. This dual-site capability accelerates startup timelines and expands subject diversity while simplifying regional approvals.

Agile, Mid-Sized Delivery Model

Unlike bloated global CROs, we offer direct access to decision-makers, faster study initiation, and personalized project management. Our lean team model ensures speed without compromise.

Academic Backbone, Operational Excellence

As a CRO powered by a clinical research school, BICS continuously trains its internal teams on evolving global regulations, trial technologies, and quality systems. The result: better-prepared teams, updated SOPs, and smoother audits.

Meet the Leadership Behind Every Trial

Our core leadership team brings medical credibility, regulatory insight, and decades of hands-on trial oversight to every study we run.

Dr. Jitendra Agrawal

Principal Investigator & Medical Director

Qualification: MBBS, MD (Medicine), Diabetes Certification–Boston University
Experience: 30+ years

80+ national/international trials

Director, Sanjeevan Hospital

Specializations: Endocrinology, Infectious Diseases

Dr. Meena Agrawal

Academic Research & Regulatory Advisor

Qualification: MBBS, MD (Physiology)
Experience: 30+ years
Highlights:

19+ international publications

Educational Director, Sanjeevan Hospital

Expert in ethics, training, compliance

CRO Services–What We Deliver

Full-service, regulatory-compliant CRO solutions with clinician-led oversight and tech-enabled execution.

Clinical Trials

Phase I-IV, monitoring & SDV, regulatory

Pharmacovigilance

ICSR, PSUR, Signal detection

Therapeutic Expertise

Diabetes, oncology, Dermatology, cardiology

Technology Backbone

CTMS, Dashboards, 21 CRF Part 11

Engagement Models

FSP, Trial Rescue, India + UAE-PI Network

Therapeutic Domain Specialization

At BICS, we support trials and safety studies across diverse therapeutic areas — with a focus on complex conditions, high-growth domains, and regionally relevant diseases.

Our India + UAE trial network, investigator-led model, and regulatory alignment ensure both subject diversity and scientific integrity across every project.

Diabetes & Metabolic Disorders

Ideal sites for long-term endocrinology trials with compliance.

Oncology & Hematology

Protocol-to-closeout support for oncology trials Biosimilar and rare cancer experience Regulatory compliance in fast-paced studies

Infectious Diseases & Vaccines

Experienced in infection trials, vaccine safety, and rapid patient recruitment network.

Nutraceuticals & Herbal Sciences

Specialized in herbal trials, Ayurveda protocols, and cosmetovigilance reporting.

Dermatology & Cosmetology

Expertise in skincare trials with flexible protocols and measurable outcomes.

Cardiology & Critical Care

Hospital-integrated trials with focus on hypertension, ICU endpoints, and real-time safety/data reporting.

Regulatory Alignment & Infrastructure

Built for Audits. Ready for Approvals.
At BICS, regulatory compliance isn’t a phase — it’s our operating standard. Across India and UAE, our trials are governed by ICH-GCP-aligned SOPs, audited sites, and secure, tech-enabled systems.

50+ Audits Passed – Zero critical findings
Ethics Committee–Registered Sites
ICH-GCP, CDSCO, MOH-UAE Compliant

50+ Audits Passed – Zero critical findings
Ethics Committee–Registered Sites
ICH-GCP, CDSCO, MOH-UAE Compliant

Engagement Models Built for Flexibility

We adapt to your trial’s complexity and scale—offering models that bring speed, control, and region-specific execution.

Full-Service CRO

We unite experts to challenge norms and drive meaningful change.

Trial Rescue

Reignite stalled trials with strategy, staffing & data review

Functional Services (FSP)

Deploy skilled BICS resources inside your SOP framework

India + UAE Site Network

One contract, two-region execution

Case Highlights / Outcome Snapshots

Real-world results across therapeutic areas and regulatory zones — delivered with medical precision.

326 patients enrolled in 9 weeks
20% budget savings
Report submitted 18 days early

PV system lives in 4 weeks
0 audit findings
Certified by MOH

92% subject retention
UAE approval in 1 submission
PV library created

Ready to Collaborate?

Get in touch to discuss how BICS can support your clinical development needs.

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