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Expert Medical Oversight for Safer, Compliant, and Efficient Trials

At DiagnoSearch, our Medical Monitoring team supports sponsors across the entire clinical development lifecycle, from early-phase trials to post-marketing surveillance. We ensure strict compliance with international and local standards, including USFDA, EMA, CDSCO, and ICH-GCP.

Medical Monitoring Services for Clinical Trials

Protocol & Regulatory Support

Our team actively contributes to

  • Study protocols (eligibility criteria, safety management, endpoints)
  • Risk management and mitigation strategies
  • Regulatory submissions (IND/CTA)
  • Medical decision-making on protocol deviations and patient management.

Real-Time Safety Oversight

  • Continuous review of AEs and SAEs
  • Close collaboration with Pharmacovigilance for timely, accurate reporting
  • Medical training for investigators, site staff, and internal teams
  • Development of clear medical training materials (slide decks, FAQs, manuals)

Medical Data Review & Analysis

  • Periodic medical data reviews with coding (MedDRA)
  • Interpretation support for interim and final analyses
  • Representation at safety and data monitoring committees
  • Sponsor representation during audits and inspections
Medical Monitoring Services for Clinical Trials

Tailored Expertise You Can Trust

Every trial is unique, and our medical monitoring services are designed to adapt. With a focus on participant safety, regulatory compliance, and data-driven decision-making, DiagnoSearch ensures your trials are conducted smoothly and delivers trusted outcomes.

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how we can support your next study.

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