Transforming Healthcare Innovation through End-to-End
Clinical Development Solutions
At Analysis Research Management Services (ARMS), we are committed to driving healthcare innovation as a leading Clinical Development Organisation (CDO) in India. Our Clinical Development venture offers comprehensive, end-to-end solutions for pharmaceutical, biotech, nutraceutical, and medical device companies, helping them accelerate product development and bring safe, effective, and market-ready products to patients worldwide.
With over 350+ successful clinical studies and 40+ state-of-the-art clinical development sites across India, ARMS combines scientific expertise, operational excellence, and ethical practices to deliver actionable insights, robust clinical data, and regulatory compliance across all product categories.
Our Clinical Development Expertise
- Regulatory Affairs & Global Compliance: Guidance for DCGI, USFDA, EMA, and other international regulatory pathways, ensuring seamless approvals and market entry.
- End-to-End Clinical Trials Management: From study design, protocol development, and site selection to patient recruitment, monitoring, data collection, and reporting, ensuring high-quality outcomes.
- Medical Devices, Topicals & Nutraceuticals: Specialized expertise to manage product-specific clinical and regulatory challenges effectively.
- Quality Assurance & Risk Mitigation: Implementation of robust quality control and auditing procedures to maintain safety, efficacy, and reproducibility.
- Medical Writing & Regulatory Documentation: Preparation of clinical study reports, regulatory dossiers, and scientific publications adhering to global standards.
Strategic Collaborations & Network
ARMS works closely with a strong network of investigators, medical experts, hospitals, and research partners, providing a collaborative ecosystem for clinical development. This ensures efficient execution, ethical governance, and accelerated timelines while maintaining high scientific standards.
Why Choose ARMS?
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Proven Track Record: 350+ clinical studies delivered with precision, compliance, and scientific rigor.
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End-to-End Solutions: Full lifecycle support from concept to market-ready product.
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Accelerated Timelines: Fast-track product development without compromising quality or regulatory compliance.
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Global Standards: Clinical development aligned with international regulatory requirements.
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Impactful Innovation: Transforming clinical data into actionable insights that improve patient outcomes and healthcare delivery.
Our Mission
To empower healthcare organizations with innovative, safe, and effective clinical development solutions, bridging the gap between research and real-world impact.
Partner with ARMS
Join a trusted Clinical Development Organization that delivers scientific excellence, regulatory confidence, and market-ready healthcare innovations. Let ARMS accelerate your product development journey and enhance your global reach in healthcare innovation.