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Zillan Clinical Research
The Future of Clinical Trial is Here
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Patients
Try Tomorrows Treatment Today
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Sponsors/CROs
Develop Game Changing Medicine
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About Zillan Clinical Research

Zillan Clinical Research is a multi-therapeutic network of clinical research sites located in United States and West Africa. We are dedicated to the expert delivery of treatment options to patients and providers. We partner with the most reputable pharmaceutical, biotechnology, and medical device companies in the world to discover and develop innovative, safe and effective ways to prevent and/or treat some of the world’s most challenging diseases.

We pride ourselves on very high PI involvement in every study from the feasibility to the investigators trainings of the entire staff to Consenting each subject. Patient safety is critical to our site so all of our staff are up to date on their GCP and a variety of certifications.

Our services are provided strictly following ICH, GCP and regulatory guidelines as well as our rigorous standards of procedures. Our expertise in volunteer recruiting and screening, and our large network of experienced investigators in several specialties, allow us to conduct trials with subjects of all types in our state-of-the-art facility, which has been carefully designed to provide maximum efficiency, safety and comfort.

Our Therapeutic Areas

We Cover A Broad Range Clinical Studies

General Medicine

Our studies cover Obesity, Pain, STI, Asthma, Hypertension, Diabetes, and Smoking.

Vaccine

Our studies cover Flu, RSV, Covid-19, and Maternal.

Women's Health

Our studies cover Pregnancy, HPV, Uterine Fibroids, Contraception, STDs and PCOS.

Dermatology

Our studies cover Atopic Dermatitis, Acne, BOTOX, Laser Treatment, Psoriasis, and Eczema.

Join A Study

Get Healthcare Through Clinical Research

Zillan Clinical Research is dedicated to revolutionizing clinical trials with innovation and quality. Our patient-centered approach, coupled with expertise in regulatory affairs, ensures the safety and satisfaction of participants while developing effective treatments for challenging diseases.

Partnering with leading pharmaceutical and medical device companies, we strive to make a meaningful impact on global healthcare.

Our Services

We Execute Clinical Trials

We offer a comprehensive range of services designed to support every stage of your clinical trial journey. From protocol feasibility and regulatory documentation to patient recruitment and site management, our experienced team is dedicated to delivering high-quality, patient-centered research solutions.

LOCATE NEW STUDIES

We will assist you in the identification and place of new studies at your facility.

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ACCOUNT MANAGEMENT

We will tract accounts receivable for work performed on studies at your facilities, and provide billing sheets for each visit during the study duration.

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PROTOCOL FEASIBILITY

We complete your feasibility submissions to Sponsors for new studies based on your patient population and facility.

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REGULATORY FILE MAINTENANCE

File, organize and maintain all regulatory files digitally to comply with FDA, Sponsor, and IRB guidelines.

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CONTRACT/BUDGET NEGOTIATION

We will negotiate with the Sponsor Company for the Clinical Trial Agreement regarding the new studies placed at your site

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REGULATORY DOCUMENTATION

We complete the initial regulatory documents for new studies based on your site

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Our Partners

We Work With The Best

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