We provide a full range of services to support clinical trials across the entire trial lifecycle, including:

• Phase II-IV Clinical Trials – Conducting advanced clinical trials with a focus on safety, efficacy, and regulatory approval.
• IIS Studies: Supporting scientific research with robust, compliant study execution.
• Post Marketing Surveillance: Assess post-launch drug performance, analyse adverse effects, understand usage across populations, ensure long-term safety, and inform label updates with real-world data for improved patient management.
• Project Management – End-to-end management of clinical trials, ensuring timely and cost-effective execution.
• Site Management – Identifying, selecting, and overseeing clinical trial sites to ensure adherence to protocols and quality standards.
• Data Management & Statistics – Efficient data collection with our inhouse EMR platform -MedSign & data management, and statistical analysis to generate reliable and actionable insights.
• Clinical Study Reports (CSRs) – Comprehensive reports detailing clinical trial methodology, results, and interpretations, meeting regulatory requirements for submission.
• Regulatory Submissions – Preparation of documents for ICF, CRF, SAP, PRO Questionnaires   EC Dossier, and other regulatory submissions, ensuring adherence to agency guidelines and standards.

At Medclin Research, we specialize in conducting Real World Evidence (RWE) studies to provide actionable insights that bridge the gap between clinical trials and everyday healthcare practices. Our RWE studies leverage real-world data to assess the effectiveness, safety, and value of medical interventions in actual clinical settings.

Our RWE Services Include Longitudinal & Cross-Sectional RWE:

• Observational Studies – Conducting cohort, case-control, and cross-sectional studies to evaluate treatments and outcomes in real-world settings.
• Patient-Reported Outcomes (PRO) – Collecting data directly from patients to assess their health status, quality of life, and treatment satisfaction.
• Epidemiological Studies – Analysing the prevalence, risk factors, and outcomes of diseases across diverse populations, helping to guide public health strategies.
• Cross-Sectional Real-World Evidence – Offering deep insights from ten years of comprehensive prescription data.

Health Economics & Outcomes Research (HEOR) – Providing cost-effectiveness and health economic evaluations to support decision-making in healthcare policy and reimbursement

At Medclin Research, our Medical Affairs team offers expert Scientific Writing & Communication services to help translate complex scientific data into clear, compelling, and regulatory-compliant documents. We ensure that your medical content is accurate, informative, and aligned with the latest industry standards.

In addition, we leverage our vast network of over 10,700 registered doctors across 80+ centers pan-India, processing around 60 lakh prescriptions annually. This extensive database provides us with the foundation to offer highly detailed and actionable insights for real-world healthcare decision-making for our cross- sectional RWE.

Our Scientific Writing & Communication Services Include:

• Scientific Manuscripts – Writing peer-reviewed articles for publication in high-impact medical journals, highlighting the clinical and scientific significance of your research.
• Medical Presentations – Creating impactful presentations for medical conferences, meetings with Key Opinion Leaders (KOLs), or internal stakeholders.
• Medical Affairs Documents – Development of scientific abstracts, posters, Leave Behind Literature (LBL), Systematic Reviews, Narrative Reviews and white papers to communicate key research findings and therapeutic advancements.
• Patient and HCP Communication – Crafting educational materials for patients and healthcare professionals, ensuring clarity and scientific accuracy.

.