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We are dedicated to expediting the development of novel drugs and devices, aiming to enhance the quality of human life worldwide by accelerating clinical trials and research initiatives.

Health Begins With Your Awareness

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At the core of our pharmacovigilance efforts lies the fostering of safe and effective health product utilization. This involves meticulous collection of adverse drug reaction (ADR) data, precise case processing, and the development of risk management plans (RMPs) and REMs. We meticulously create and submit expedited and aggregated pharmacovigilance reports, emphasizing shared responsibility for safer healthcare practices.

Pharmacovigilance Services

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Our biospecimen collection comprises diverse human samples—bio-fluids like blood, serum, urine, saliva, tissues, and cells—enabling robust clinical drug development research in Oncology, Neurology, Infectious Diseases, Cardiology, Rheumatology, and Reproductive health. Our comprehensive array ensures varied options to suit your research needs across these therapeutic areas

Biospecimens Collection Services

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IQVAMED is committed to establishing an adhocracy culture in which our mission, leadership, and collaboration are appreciated, and every employee has the equal opportunity to contribute their full potential and integrity to achieve their personal goals and career expectations

Explore your career with IQVAMED

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IQVAMED Defines Excellence in Delivery.

IQVAMED is a leading Clinical Research Support Organization (CRSO)/ Outsourced healthcare service provider based in Mumbai, India. We specialize in delivering comprehensive end-to-end services to sponsors within the pharmaceutical, biotechnology, and medical device industries. Our offerings encompass a wide array of solutions and services, including clinical trial and research management activities, aimed at supporting our clients’ pursuit of advancements for a healthier world.

 

Integrated Services for Innovation: At IQVAMED, we seamlessly integrate three core services—Clinical Research, Pharmacovigilance, and Biospecimens Collection—to foster a perpetual cycle of innovation. Biospecimen analysis yields invaluable insights that often serve as catalysts for the development of groundbreaking drugs. These potential breakthroughs then undergo meticulous clinical trials managed by our expert team. Post-launch, our Pharmacovigilance division diligently evaluates the safety and efficacy of these drugs, completing a cohesive loop essential for maintaining the highest standards of patient care and industry excellence.

 

Driving the Pursuit of Healthier Lives: Our commitment at IQVAMED extends beyond providing services; we are dedicated to driving advancements that contribute to the global pursuit of healthier lives. By facilitating research and development within the pharmaceutical and biotechnology sectors, we actively contribute to shaping a brighter future for healthcare worldwide.

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Explore Our Solutions

Leverage our expertise to enhance clinical development.

Optimize your clinical trial development through ethical standards, quality-driven processes, and tailored services designed to meet your project requirements. We strive to mitigate risks through robust quality management, ensuring patient safety, responsiveness, adaptability, and meticulous oversight throughout trial execution and site management.

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Reducing workload and improving efficiency at clinical sites.

We provide customized SMO services to help our clients reach the right patient population efficiently. Our experienced research coordinators deliver comprehensive site-level support, ensuring that each clinical trial is conducted in accordance with ICH-GCP guidelines, New Drugs and Clinical Trials Rules (NDCTR), 2019, and all applicable regulatory requirements.

Our services include:

  • Site start-up and activation support
  • Investigator and site identification support
  • Site feasibility assessment and selection support
  • Ethics Committee (EC) submission and coordination
  • Patient recruitment and retention support
  • Site staff training and GCP compliance support
  • Study coordination & site-level project management support
  • Monitoring visit coordination and query resolution support
  • Data collection support and source document management
  • Site close-out support and documentation archiving

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Real-world data define real-world insights.

We offer a comprehensive suite of non-interventional study services, covering every aspect of project requirements. Our solutions support hospitals, pharmaceutical, biotechnology, and medical device companies in generating meaningful real-world evidence to support clinical and regulatory decision-making.

Our services include:

  • Post-authorization safety studies (PASS)
  • Post-marketing surveillance (PMS) studies
  • Cohort and case-control studies
  • Risk Management Plans  (RMP) support.
  • Real-World Data (RWD) collection and management.
  • Disease registry design, setup, and management.

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Our breadth of vision is aligned with accomplishing your mission.

IQVAMED delivers end-to-end pharmacovigilance (PV) services through strong operational expertise and diversified core competencies. Our professionals possess extensive experience and a broad skill set in managing key pharmacovigilance functions, ensuring regulatory compliance, patient safety, and high-quality safety surveillance across the product lifecycle.

Core Capabilities:

  • Adverse Event Case Management.
  • Expedited Reporting,
  • Aggregated Reporting,
  • Signal Intelligence: and
  • Risk Management.

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Biospecimens collection services
ePRO Solutions
Site Personnel Training

Clinical Site Feasibility

Optimize Sites. Accelerate Trials.

At IQVAMED, our Clinical Site Feasibility Services ensure your multicentre clinical trials in India begin with data-driven, high-performing sites. We evaluate site capability, investigator experience, patient availability, and operational readiness to support accurate and confident site-selection decisions.

We help sponsors identify qualified, compliant, and research-ready sites through a comprehensive feasibility approach:

  • Identification of potential sites across multiple therapeutic areas
  • Assessment of investigator and site staff experience
  • Infrastructure, equipment, and facility capability evaluation
  • Patient pool and recruitment potential analysis
  • Regulatory & Ethics Committee (EC) readiness assessment
  • Review of site’s past performance and compliance metrics
  • Collection and verification of essential documents
  • Feasibility insights and ranking for optimized site selection
IQVAMED Clinical Site Feasibility

Medical Writing

Clear. Compliant. Credible.

At IQVAMED, our Medical Writing Services support clinical research and regulatory submissions with scientifically accurate, regulatory-compliant, and well-structured documents. We help transform complex scientific data into clear, concise, and impactful content for regulatory agencies, healthcare professionals, and patients.

We specialize in writing high-quality documents essential for drug and device development, submission, and approval:

  • Clinical Study Protocols (CSP)
  • Protocols and Amendments
  • Investigator’s Brochure (IB)
  • Clinical Study Reports (CSR)
  • Informed Consent Forms (ICF)
  • Common Technical Documents (CTD Modules: 2.5, 2.7, etc.)
  • Annual Safety Reports (DSUR, PSUR, PBRER)
IQVAMED Medical Writing

Biostatistics Services

Turning Data into Evidence, and Evidence into Insight.

At IQVAMED, our Biostatistics Services deliver scientifically sound, regulatory-compliant statistical solutions for clinical trials across all phases. From protocol design to submission-ready statistical reports, our team ensures that your clinical data is interpreted accurately, efficiently, and with statistical rigor.

  • Study Design & Statistical Consulting
  • Statistical Programming (SAS, R, Python)
  • Data Analysis & Interpretation
  • Submission Support & Reporting
  • Experienced Statisticians: Experts with global trial experience.
  • Regulatory Expertise: CDISC-compliant outputs and submission-ready packages.
  • Data Integrity: Strict QC processes and reproducibility of results.
IQVAMED Biostatistics Services

PV Audit Services

Ensuring Drug Safety with Compliance, Accuracy & Confidence

IQVAMED offers a full range of Pharmacovigilance audit services in accordance with good pharmacovigilance practices (GVP) requirements and global regulations.

In addition to our standard comprehensive system GVP auditing services, IQVAMED offers a flexible and customizable GVP auditing service that can cover one or multiple sectors on a global scale. Our team of experienced pharmacovigilance professionals can tailor our auditing services to meet the specific needs of our clients in the pharmaceutical, biotech, and medical device industries.

  • System & Process Audits
  • Case Processing Audits
  • PMS & Aggregate Report Audits
  • Third-Party / Vendor Audits
  • Inspection Readiness Support
IQVAMED PV Audit Services

Functional service

Our functional services deliver a diverse range of functional expertise, and management solutions to execute core competencies and propel the process of clinical development for your outsourced project.

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Therapeutic Areas Phase II-IV

At each stage of the drug development process, IQVAMED demonstrates the safety and efficacy of novel therapeutics and executes your clinical trials as per ethical standards and unwavering commitment to quality.

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IQVAMED

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The Capital, Level 7, Plot No C-70, G Block, Bandra Kurla Complex (BKC) Bandra (East) Mumbai – 400051 MH India

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