ABOUT US

Analysis Research Management Services (ARMS) is a trusted Workforce Management & Site Support Organization with several years of experience in the clinical research industry. Established with a vision to strengthen site-level operations and empower sponsors, CROs, and investigators, ARMS has become a reliable partner in ensuring that clinical trials are conducted with efficiency, compliance, and global quality standards.

We specialise in providing highly skilled manpower – Clinical Research Associates (CRA), Quality Assurance (QA), and Quality Control (QC) professionals – who are trained to deliver site-level excellence. Our dedicated teams ensure that every clinical trial site we support is audit-ready, compliant with ICH-GCP, and aligned with international regulatory expectations (USFDA, EMA, MHRA, DCGI, WHO).

At ARMS, we go beyond staffing. We provide operational confidence by integrating our expertise into site workflows, strengthening documentation, ensuring data accuracy, and facilitating smooth sponsor/CRO interactions.

OUR EXPERTISE

Clinical Research Associates (CRA)

Our CRAs ensure clinical sites maintain the highest standards of trial conduct. They handle site monitoring, source data verification, protocol adherence, patient safety oversight, and issue resolution, acting as the connecting bridge between sites and sponsors/CROs.

Quality Assurance (QA)

Our QA experts provide systematic oversight through internal audits, SOP compliance, CAPA management, and pre-inspection readiness. With a proactive approach, they identify and resolve gaps before regulators do, ensuring sites are always prepared for sponsor audits, regulatory inspections, and accreditation reviews.

Quality Control (QC)

Our QC teams strengthen data integrity by reviewing trial documentation, patient records, and site files. They minimise risks during inspections by improving accuracy, reliability, and reporting standards.

Site Management Support

We provide end-to-end site management services – study start-up, patient recruitment, documentation, and ongoing operational support – ensuring efficient site performance and sponsor satisfaction.

WHY PARTNER WITH ARMS?

✔️ 10+ Years of Experience – Proven decade-long track record in clinical research support.
✔️ Audit & Inspection Readiness – Expertise in sponsor audits and regulatory inspections (USFDA, EMA, MHRA, DCGI).
✔️ Skilled Manpower – Well-trained CRA, QA, and QC professionals with hands-on therapeutic experience.
✔️ Operational Excellence – Streamlined processes that reduce timelines, improve compliance, and enhance outcomes.
✔️ Global Standards Alignment – Fully aligned with ICH-GCP, USFDA, EMA, MHRA, WHO, and DCGI guidelines.
✔️ Multi-site Experience – Currently supporting 10+ active clinical trial sites with ongoing sponsor collaborations.
 

OUR VISION & COMMITMENT

At ARMS, our vision is to become the most trusted Site Management Partner for global sponsors and CROs. We are committed to delivering:

• Excellence in Site Operations – through expertise, training, and continuous improvement.
• Compliance & Integrity – by upholding the highest ethical and regulatory standards.
• Value for Clients – by ensuring cost-effectiveness, reduced risks, and efficient site operations.

We don’t just provide manpower – we provide assurance that your sites are fully prepared for success.

RECOGNITION & EXPERIENCE

• 3 Successful USFDA Audits – with smooth conduct and Zero 483 Findings, resulting in a USFDA appreciation letter for operational excellence.
• 6 Successful DCGI Audits – demonstrating consistent compliance and inspection readiness.
• 350+ Clinical Studies Supported across diverse therapeutic areas.
• 26 Active Clinical Trials Managed across 10 sites in Varanasi with a team of 26+ trained Clinical Research Coordinators and monitoring staff.
• Proven partner for audit clearance, CRO collaboration, and clinical site upgradation.