Testimonials

"Best Quality Research have assisted in many aspects of trial management and logistics including negotiating with CROs, and study start up activities, recruitment, budgeting, document review, etc. We have found Best Quality Research to be an excellent, efficient, effective and pro-active team of highly skilled individuals. Our experiences have been very positive and our objectives have been achieved. Highly recommend Practical Clinical."...

Andrew

Our Staff Have More Than 30 years of Experience

Located less than 1 mile from the Palmetto General Hospital.

Best Quality Research is a contract research organization ("CRO") that provides clinical research, data management, statistical and reporting services to the pharmaceutical and related industries.

Best Quality Research was founded in 2012 and operates Phase II through IV clinical endpoint studies. We understand research and know how to make sure it is done right with experienced staff and a professional, caring environment for our patients with an averages over 200 Phase studies performed annually.

A. Each team is made up of Clinical Research Associates, Regulatory Affairs staff, Document Control clerks, Quality Control experts and a team from our Data Management Group.
B. Best Quality Research has developed expertise in performing studies with non-traditional delivery systems such as topical transdermal, nasal, inhaled, rectal, vaginal, and intravenous routes of administration.
C. Currently focus on performing Phase II through IV clinical endpoint studies requiring large patient populations in non-serious disease states that are treated in an outpatient setting.

Quality Standards

Quality of clinical trials depends on data integrity and subject protection. Globalization, outsourcing and increasing complexicity of clinical trials have made the target of achieving global quality challenging. The quality, as judged by regulatory inspections of the investigator sites, sponsors/contract research organizations and Institutional Review Board, has been of concern to the US Food and Drug Administration, as there has been hardly any change in frequency and nature of common deficiencies. To meet the regulatory expectations, the sponsors need to improve quality by developing systems with specific standards for each clinical trial process.

How it Works

1
Phase I trial
Researchers test an experimental drug or treatment in a small group of people (20-80) for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
2
Phase II trial
The experimental treatment is given to a larger group of people (100-300) to see if it is effective and to further evaluate its safety.
3
Phase III trial
The treatment is given to large groups of people (1,000-3,000) to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow it to be used safely.
4
Phase IV trial
Postmarketing studies delineate additional information, including the treatment's risks, benefits, and optimal use. Before pharmaceutical companies start clinical trials on a drug, they conduct extensive preclinical studies.