Global CROs Solutions

Our Offerings

     Pre-Clinical Services

Our pre-clinical services encompass comprehensive in vitro, pharmacology, and toxicology studies, supported by a CCSEA-approved animal research facility. With dedicated Study Directors, we ensure rigorous and compliant research that drives meaningful outcomes.

     Project Management

Our project management services cover every aspect of clinical trial execution, from patient recruitment to study data reporting. We handle resource management, budgeting, and vendor management with precision, ensuring seamless coordination and successful study outcomes.

      Regulatory Services

Our 360-degree approach ensures our regulatory team is always available to guide you through every step. With vast experience in FDA, EMA, MHRA, and CDSCO regulatory bodies, We do multinational submission of your clinical trial applications, handle import/export, transparency services, and safety reporting.

     Site Facility Services

Our site facility capabilities include a network of over 300+ experienced clinical investigators and sites, ensuring high-quality trial execution. We provide comprehensive services from site feasibility assessments to site selection, activation, and management, ensuring optimal site performance and study success.

       Clinical Operations

Our clinical operations team excels in managing all phases of clinical trials, from planning and execution to monitoring and reporting. With a focus on efficiency and quality, we ensure smooth trial conduct and successful study outcomes

Clinical Data Management

Our Clinical Data Management capabilities include robust data collection, validation, and analysis, ensuring high-quality, accurate data throughout the trial. With advanced systems and experienced professionals, we deliver reliable data that supports informed decision-making and regulatory compliance.

Biostatistics & Analytical

Our Biostatistics & Analytical services offer comprehensive statistical analysis, study design support, and data interpretation. We provide precise, data-driven insights that are crucial for making informed decisions and achieving successful trial outcomes.

  Medical Writing Services

Our medical writing team specializes in Development of essential clinical trial documents, including Protocols, Investigator Brochures (IB), Informed Consent Documents (ICD), and Clinical Study Reports (CSR). We ensure that each document is meticulously prepared to support successful trial outcomes.

       Pharmacovigilance

Our PV Services including continuous safety monitoring, adverse event reporting, and risk assessment. Our expertise ensures that drug safety is meticulously tracked and managed, helping to meet regulatory requirements and safeguard patient well-being.

          BA/BE Services

Our Bioavailability (BA) and Bioequivalence (BE) services are designed to support the development of both generic and novel formulations. We conduct rigorous studies to compare the absorption and effectiveness of different drug formulations, ensuring they meet regulatory standards for approval.

     Bioanalytical Services

We offer state-of-the-art bioanalytical services using advanced techniques for precise measurement of drug levels and biomarkers. Our capabilities include method development, validation, and sample analysis, providing reliable data essential for pharmacokinetic and pharmacodynamic studies.

            Quality Services

Our Quality Assurance services focus on maintaining the highest standards of compliance and data integrity. We implement comprehensive QA protocols to ensure adherence to regulatory guidelines, enhance research quality, and support successful trial outcomes.

Delivering Excellence to World...

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