Welcome to CliniSMS Research Services Pvt. Ltd.

CliniSMS is a leading Site Management Organization (SMO) based in Chhatrapati Sambhajinagar (Aurangabad), Maharashtra, providing end-to-end clinical trial support to CROs, pharmaceutical, biotechnology, and medical device companies. With extensive experience across Phase I–IV clinical trials, BA/BE studies, and medical device research, we are committed to delivering reliable, compliant, and efficient site management solutions.

At CliniSMS, we strive to be your trusted partner—offering expertise, integrity, and dependable support throughout every phase of your clinical research journey.

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Therapeutic Areas

Advanced Therapeutic Expertise

Delivering expert support across multiple therapeutic areas with scientific accuracy, skilled teams, and reliable outcomes.

Oncology & Hemato-Oncology

Gastroenterology & Hepatology

Endocrinology & Diabetology

Obstetrics & Gynecology

Orthopaedics

General Medicine

Cardiology

Dermatology & Cosmetology

Our Strengths

Combining expertise, infrastructure, and innovation to deliver exceptional clinical trial management and reliable results.

Fast & Efficient Execution

Rapid site start-up and streamlined execution processes

Experienced Investigators

Access to specialists across multiple therapeutic areas

World-Class Facilities

USFDA-inspected, NABH approved multispecialty centers

Strong Patient Recruitment

Proven recruitment & retention strategies for success

Expert Clinical Team

Dedicated, trained & experienced operations professionals

Competitive Cost Model

Cost-effective solutions without compromising quality

Professional Partnership

Transparent and collaborative approach to every project

Our Services

Delivering trusted, efficient, and end-to-end clinical research services designed to support high-quality global studies.

Excellence in
Clinical Research

Trusted by pharmaceutical and biotech companies worldwide for reliable, ethical, and high-quality trial management.

Why Choose CliniSMS

Experienced Professionals & Site Staff

Our team consists of highly trained site managers with extensive experience in clinical trial management across various therapeutic areas.

Regulatory Compliance

We ensure that all clinical trial activities adhere to the latest regulatory standards and guidelines, minimizing risks and ensuring data integrity.

Streamlined Processes

Our efficient site management processes are designed to optimize patient recruitment, data collection, and overall trial performance.

Patient-Centric Approach

We prioritize patient safety and well-being, implementing robust protocols to ensure ethical conduct and patient satisfaction.

Comprehensive Support

From site selection and initiation to monitoring and close-out, we provide end-to-end support to ensure your trial's success.

Our Core Values

Guiding principles that define how we conduct every clinical study with trust, clarity, and scientific excellence.