Site Management Organization

Advancing Clinical Excellence with Trusted Research Solutions

Elite CRS delivers comprehensive, end-to-end clinical trial execution across Phase I–IV studies, built on rigorous quality, regulatory compliance and unwavering patient safety.

Explore Capabilities

About Elite CRS

A Site Management Organization built on quality, reach and accountability

We are a dedicated Site Management Organization committed to delivering comprehensive clinical trial solutions, combining clinical depth with the operational discipline sponsors and CROs expect.

Site Management Organization

A leading SMO dedicated to delivering comprehensive clinical trial solutions with unwavering commitment to quality and patient safety.

End-to-End Support

Complete clinical trial support spanning Phase I through Phase IV studies, including specialized PK/PD investigations, nutraceutical trials and cosmeceutical research programs.

Quality & Compliance

Uncompromising focus on quality assurance, regulatory compliance and patient safety protocols meeting international standards and best practices in clinical research.

Pune • Nashik • Malegaon • Dhule

Maharashtra, India

Our Strategic Presence

Geographic Coverage

Elite CRS operates from strategically located centers in Pune, Nashik, Malegaon and Dhule, Maharashtra, giving us extensive reach across the region. Our locations offer strong accessibility for patient recruitment and trial execution while staying close to major healthcare facilities and research centers, enabling efficient multi-center trials and robust data collection across therapeutic areas.

Hospital Network

We've built strong partnerships with private, trust-run and government multispecialty hospitals across our operating regions, giving sponsors access to qualified investigators, specialized facilities and diverse patient populations, with seamless coordination and efficient patient management throughout.

Capabilities

Comprehensive clinical trial services

A complete suite of services designed to support sponsors, CROs and pharmaceutical companies throughout the entire trial lifecycle.

Clinical Trial Execution

End-to-end site management and trial execution ensuring protocol adherence, timeline management and efficient study conduct from initiation to completion.

Patient Recruitment

Strategic recruitment and retention programs using proven methodologies and community outreach to ensure adequate enrollment and compliance.

Regulatory Coordination

Comprehensive regulatory and ethics committee management, including document preparation, submission and ongoing communication with regulatory authorities.

Data Management

Comprehensive data management processes ensuring accurate data capture, timely query resolution and adherence to GCP guidelines throughout the study lifecycle.

Monitoring Support

Dedicated support facilitating smooth site visits, query resolution and real-time issue management to protect study integrity and compliance.

Referral Network

An extensive consultant referral network across multiple specialties, enabling efficient patient identification, screening and enrollment.

Medical Writing

Skilled preparation of protocols, informed consent documents, clinical study reports and regulatory submissions with scientific accuracy and clarity.

Why Choose Us

Infrastructure and discipline sponsors can rely on

We've invested in the facilities and quality systems complex trials demand, built to international standards for clinical research execution.

Internal QC & QA

Regular audits and source document verification ensuring protocol adherence and data integrity.

GCP Compliance

Full adherence to Good Clinical Practice, protecting patient rights and data quality.

Audit Readiness

Systematic documentation and proactive issue resolution keep us audit-ready at all times.

Documentation

Complete, contemporaneous record-keeping with version control and signature verification.

  1. 01

    Institutional Ethics Committee

    On-site IEC facility for timely protocol review and rapid study initiation.

  2. 02

    IP & Document Storage

    Secure investigational product storage with controlled access and temperature monitoring.

  3. 03

    Document Archival

    Dedicated long-term storage for essential trial documents and regulatory submissions.

  4. 04

    Monitoring Room

    Private space for sponsor & CRO visits.

  5. 05

    Study Coordinator Room

    Dedicated workspace with systems and documentation for efficient coordination.

  6. 06

    IMP Preparation

    Specialized preparation and dosing room with emergency readiness protocols.

  7. 07

    NABL Accredited Labs

    Access to accredited pathology labs with validated methods and quality control.

  8. 08

    Accredited Radiology

    Partnership facilities offering X-ray, CT, MRI and ultrasound as protocols require.

  9. 09

    Blinded Study Infrastructure

    Procedures supporting both blinded and unblinded designs, preserving protocol integrity.

0 Years of Combined Experience
0 Specialties Covered
0 Completed Studies
0 Trial Phases Supported (I–IV)

Therapeutic Area Expertise

Diverse protocols. Diverse patient populations.

We've executed clinical trials across a comprehensive range of therapeutic areas, spanning common and specialized conditions alike.

Cardiology

Cardiovascular disease, hypertension, heart failure, arrhythmias.

Dermatology

Skin disorders, acne, psoriasis, eczema, cosmetic dermatology.

Endocrinology

Diabetes, thyroid disorders, metabolic syndrome, hormonal imbalances.

Gastroenterology

Digestive disorders, liver disease, IBD, IBS, GI malignancies.

Hematology

Blood disorders, anemia, coagulation and hematological malignancies.

Immunology & Infectious

Autoimmune disease, immunodeficiency, infections, vaccination studies.

Nephrology / Urology

Kidney disease, renal failure, urinary tract and urological conditions.

Neurology

Stroke, epilepsy, Parkinson's, Alzheimer's, migraines.

Oncology

Various cancers, chemotherapy, targeted therapy, immunotherapy.

Ophthalmology

Glaucoma, cataracts, retinal disease, vision-related conditions.

Orthopedics

Musculoskeletal disorders, arthritis, fractures, joint replacements.

Pediatrics / Neonatology

Childhood diseases, developmental disorders, neonatal care.

Pulmonary / Respiratory

Asthma, COPD, respiratory infections, pulmonary function studies.

Psychiatry / Psychology

Depression, anxiety, schizophrenia, behavioral conditions.

Rheumatology

Autoimmune rheumatic disease, arthritis, lupus, connective tissue.

General Medicine

Primary care conditions, preventive medicine, multi-system disorders.

Gynecology & Reproductive

Women's health, reproductive disorders, fertility.

Pharmacology / Toxicology

Drug metabolism, pharmacokinetics, bioavailability, safety assessment.

Leadership

Led by clinical and research expertise

Our co-directors bring complementary strengths, surgical and clinical research leadership, to every study we run.

Dr. Ajinkya Desale

MS Orthopedics, PGDCR — Co-Director

Brings surgical expertise and clinical research leadership to guide trial execution and quality standards.

Ms. Yogita Purkar

MSc Clinical Research — Co-Director

Provides clinical research methodology expertise and operational management for comprehensive trial support.

Our Clinical Delivery Team

Study Coordinators

Experienced coordinators managing multiple protocols with strong GCP grounding.

Trained Nurses

Qualified staff trained in trial procedures, patient care and protocol requirements.

Phlebotomists

Skilled in sample collection, processing and adherence to handling protocols.

Pharmacist

Registered pharmacist ensuring proper handling and dispensing of IMPs.

Partner With Elite CRS

Let's talk about your next clinical trial

For reliable, efficient and high-quality clinical research execution that advances medical science while prioritizing patient safety and regulatory compliance.

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