Site Management Services

Site Management Services
(SMS)

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We Are Thirilled To Work & Collaborate With You

IQVAMED assists CRO/Sponsor’s outsourced clinical trials by Experienced and dedicated Clinical Research coordinator (CRC) at the site as per specified therapeutics areas of assigned Protocol under the direction of the clinical investigators. Our extremely competent CRCs handles the bulk of daily clinical trial activities and plays a critical role in study conduct. IQVAMED offer training opportunities for CRCs, both through the formal presentation and the informal interactions with the sponsor’s Clinical Research Associate (CRAs) and other highly experienced clinical research professionals as per specialized therapeutics sound to study execution at the sites.

Our experienced research coordinators offer diverse capabilities to ensure each clinical trial is conducted at the sites as per ICH-GCP in accordance with the ethical principles that have their origin in the Declaration of Helsinki, and that are consistent with the Good Clinical Practice (GCP) and the applicable regulatory requirement(s) or New Drugs and Clinical Trials Rules-2019.

Why You Should Outsourced clinical trials to the IQVAMED for SMS activities?

Rapid patient recruitment.
Accurate and consistent documentation.
Reduced study timelines due to quicker study start-up.
Reduced site management time.
Improved relationships with investigators and cost effective.

Our SMS services provide for Contract Research Organizations (CRO’s), pharmaceutical, biotechnology, and medical device companies and even clinical research sites and We give customized services to our clients in order to reach the right population

Our Core Competencies

Clinical project feasibility.
Potential Sites & Investigators selection.
Submission and Notification of trials documents for Institutional Review Board or Institutional Ethics Committee (IRB/IEC) Approval and Acknowledgement.
Recruitment of study Subjects.
Participated Subjects follow up.
Informed consent form (ICF) customization.
Investigator Study Files Management.
Subject Compliance & Noncompliance Management.
Allocated Vendors Management.
Study Invoices Management.
Sites Quality Assurance/Audit Management.

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IQVAMED believe in Collaboration rather than competition in the business world. We have a single quote for all clients that is “How can we help You?”

Our Edge in Site and Patient Support

Our CRCs have expertise in various therapeutic areas.

Clinical Research Coordinator

The CRC has multiple responsibilities to manage the clinical research/trials at the sites and interact with sponsor personnel to resolved the queries.

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Clinical Site Administration

IQVAMED provides clinical site administration support for reducing the workloads of Clinical Research Coordinators at the Investigator site.

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Our CRCs have expertise in various therapeutic areas

Our Edge in Site and Patient Support

Clinical Research Coordinator

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Clinical Site Administration

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Our Focus Therapeutic Areas Phase II-IV

We are collaborative and consultative, yet acutely focused on a core set of therapeutic areas

Oncology

Cardiology

Urology

Gastroenterology

Hepatology

Hematology

Immunology

Neurology

Metabolic Disease

Endocrinology

Nephrology

Respiratory

Neurology & Psychiatry

Ophthalmology

Vaccine & Virology

I’m passionate about fostering a culture where our leadership & collaboration are celebrated, and every individual has the equal opportunity to contribute their potential and integrity for the success of IQVAMED.

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IQVAMED

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Clinical Research Services

Pharmacovigilance Services

Patient & Healthcare Services