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.
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.
PROTOCOL FEASIBILITY
We complete your feasibility submissions to Sponsors for new studies based on your patient population and facility.
REGULATORY FILE MAINTENANCE
File, organize and maintain all regulatory files digitally to comply with FDA, Sponsor, and IRB guidelines.
CONTRACT/BUDGET NEGOTIATION
We will negotiate with the Sponsor Company for the Clinical Trial Agreement regarding the new studies placed at your site
REGULATORY DOCUMENTATION
We complete the initial regulatory documents for new studies based on your site