Clinical offerings include Site Selection & Feasibility, ensuring the identification of ideal study locations with the right resources, patient availability, and operational readiness. Study Coordination supports smooth execution by managing communication, scheduling, documentation, and day-to-day trial activities. Data Management ensures that all collected information is accurate, validated, secure, and compliant with regulatory expectations. Quality Oversight continuously monitors processes, performance, and protocol adherence to maintain the highest standards of safety, reliability, and study integrity from start to finish.
SOP Writing ensures that every process is clearly documented to maintain consistency, compliance, and operational efficiency. Site Regulatory Document preparation involves organizing and submitting all essential forms, approvals, and ethics documents required for site activation. Medical & Scientific Content development focuses on creating accurate, research-based material that supports clinical studies, education, and communication. Research Paper Writing delivers well-structured, evidence-driven manuscripts suitable for publication, helping present study findings with clarity, impact, and scientific credibility.
EC Regulatory Submission Support ensures accurate preparation and timely submission of documents required for ethical approvals. Ethics Committee Registration involves guiding sites through the complete registration process to meet regulatory standards. Safety Reporting Support manages the collection, assessment, and submission of safety-related information throughout the study. Audit & Inspection Readiness helps teams prepare for regulatory audits by reviewing documentation, identifying gaps, and ensuring full compliance with guidelines.
Clinical Research, CDM & PV Course & Certification provides structured training to build strong foundations in clinical trials, data management, and pharmacovigilance. Clinical Research Internship offers hands-on exposure to real-world processes, enhancing practical understanding and industry readiness. Skill Enhancement Sessions focus on developing essential professional competencies such as communication, documentation, and technical skills. Clinical Research Workshops deliver interactive, expert-led learning experiences designed to deepen knowledge and strengthen job-oriented capabilities.
CliniSMS Research Services Private Limited is a full-service Site Management Organization (SMO) based in Chatrapati Sambhajinagar (Aurangabad),Maharashtra, providing end-to-end clinical trial support to the pharmaceutical, biotechnology, and medical device industries.
S. NO. 09, Malkhare Clasfic, Garkheda, Chatrapati Sambhajinagar (Aurangabad) Maharashtra-431001, India.
Mohan Sirsat
(Director & CEO)
+91 9730153671
info@clinismsrs.com