Tanya Evans, MD
Principal Investigator
Dr. Evans has over 15 years of experience in clinical research and development.
Avance Clinical TrialsYour trusted source in clinical trials
Avance Clinical Trials
Our strategic approach to research management enables us to provide our sponsors (pharmaceutical
companies and contract research organizations (CROs)): experienced staff, accurate patient population,
and high quality documentation adhering to regulatory compliance. All our staff is experienced and
trained to handle unique experimental designs of different trials.
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We conduct Phase II to Phase IV trials
We provide well trained and experienced study coordinators along with required ancillary staff
Conduct all activities related to the trial – including but not limited to pre-screening patients to qualify for the trial, scheduling patient visits, assisting with informed consent, randomization, dispensing drugs, drug accountability and reconciliation, conducting labs, collecting and shipping specimens, drug storage, temperature monitoring and facilitating monitoring visits
Yes we provide standard operating procedures for all the critical activities.
We complete regulatory documents with rapid turnaround time.
Yes, we finalize budgets and contracts quickly through our centralized operations
We know how burdensome it is to conduct a clinical trial without qualified staff. Our goal is to alleviate the burden associated with conducting the clinical trial allowing you to focus on your contribution to research.
Avance Clinical Trials is affiliated with Southern California Skin and Laser (SCSL) and conducts clinical research in the specialty area of Dermatology. Dr. Tanya Evans is the Principal Investigator at Avance with over 15 years of experience in clinical research and development.
At Avance, we also coordinate and provide managerial supervision for conducting the research. We provide staffing to conduct the trial – Study coordinator, MA and Quality Control / Quality Assurance specialist. Avance takes care of A-Z details of conducting a clinical trial – finding the study that matches the patient population, negotiating budgets and contracts, all the regulatory affairs, getting the clinic qualified and initiating a study, pre-screening and screening patients, scheduling patient visits, conducting all the labs, handling samples, recording data and facilitating site monitoring and audits, maintaining patient binders and regulatory binders as well as long term archival of the study materials.
Dr. Evans has over 15 years of experience in clinical research and development.
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