Health Begins With Your Awareness

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

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

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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Health Begins With Your Awareness
Pharmacovigilance Services
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Biospecimens Collection Services
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Explore your career with IQVAMED
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.
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A Celebration for International
Clinical Trials Day
In honor of ICT Day on May 20, we showcased powerful stories behind the patients we serve and our colleagues who Do It With HeartTM
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Putting patients at the heart of everything we do
Parexel is in the business of improving the world's health. As a leading CRO, we provide a suite of biopharmaceutical services that help clients across the globe transform scientific discoveries into new treatments.
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A career with a human touch
We know just how important it is to put people first. It requires a team of different perspectives working together to understand patients – who they are, and what they need. It demands the flexibility to build our best selves outside of work, so we can bring them to work.
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IQVAMED Define Excellence for Ethics.

IQVAMED is a leading CRO/Outsourced development 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.

Explore Our Solutions

Leverage the expertise to improve clinical development.

Optimize your clinical trials development by ethical standards, quality-based, and tailored services to achieve optimum results for your project requirements. We strive to mitigate risks with proper strategy management, patient safety, responsiveness, adaptability, and attention throughout the trial and sites management. Learn More

Accelerate your Operations with successful Execution.

Our competent team and operations professionals have extensive knowledge of ethical and regulatory requirements for managing and accelerating Interventional studies (Phase II -IV) from study start-up activities to maintenance and closeout.   Planing->Start-up->Submission->Initiation->Enrollment->Conduct->Cleaning- >Closeout. Learn More

Real-life data define Real-life Insight.

We provide a comprehensive range of Non-interventional studies services and every aspect of project retirements solutions to our clients (Hospital, Pharmaceutical, Biotechnology, & Devices Companies).

Services Include

  • Post-authorization safety studies (PASS),
  • Post-marketing surveillance studies (PMS),
  • Data collection & Disease Register studies,
  • Cohort and case-control studies,
  • Risk Management Plans (RMP).
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Impatient to reduce the workloads at the clinical sites.

We give customized services to our clients in order to reach the right population. Our experienced research coordinators offer diverse capabilities to ensure each clinical trial is conducted at the sites as per ICH-GCP, New Drugs and Clinical Trials Rules-2019 and applicable regulatory requirements. Learn More

Our breadth of vision is willing to complete your mission.

IQVAMED delivers end-to-end pharmacovigilance (PV) services to our clients through diverse expertise and core competencies in operation management. Our professionals have extensive experience and diversified skills in managing core capabilities of pharmacovigilance.

Core Capabilities:

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

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Biospecimens collection services
New Drug CT Rules 2019
Informed Consent of Trial Participants

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.