ABOUT US

Welcome to Prolific

Prolific is an Investigator-based coordinating agency for supporting successful completion of clinical trials for the Pharmaceutical, Biotechnology, and Medical Devices industries.

With India poised to become the leading destination for clinical trials, it is imperative that trials are conducted with highest ethical and quality standards. Though there is a huge potential, in reality very few centres are conducting clinical trials. Major challenges being faced by the industry is a lack of GCP trained investigators and trained support staff to facilitate trial conduct.

QUALITY RESOURCING

managing the trial in a cost effective way at the same time ensuring highest quality standards

QUALITY RESOURCING

We strive to use modern technologies and the latest resources in our work.

EXPERIENCED CONSULTANTS

Every team member has over five years of experience in business.

SOLUTION DEFINING

When you don’t see the right decision, we are here to show you ones.

Who We Are

All the staff must undergo continuous training through their entire period of employment Employees must complete a minimum hours of the required training before starting or changing jobs.
Our network is of highly qualified and enthusiastic Investigators who represent virtually all specialty areas. It is not just the strength and commitment of our Investigators that is the foundation of our success, but the experience and dedication of the Clinical Research Coordinators assisting these investigators in the preparation and conducting of these trials.

Prolific with its extensive knowledge provides world class services to pharmaceuticals, biotechnology companies, medical device companies, and CRO’s. The services can be tailored specifically for each project with an objective of managing the trial in a cost effective way at the same time ensuring highest quality standards.
Our Multidisciplinary Team is qualified to deliver clean and reliable data by tracing key performance indicators through the life cycle of the project and constantly assessing risks.

Who We Are

Prolific places qualified Clinical Research Coordinators who have the skills and capabilities to assist the investigator and coordinate administrative activities at the trial site. Our database have qualified, pre-screened, Principal Investigators for participation in clinical trials in virtually any specialty area.
Investigator/Site Selection procedure:
All of the Investigators have been evaluated to ensure they are adequately qualified to conduct clinical trials backed by the patient population and administrative capabilities. This eliminates a significant amount of time and expense incurred during site selection.

Ensure timely and accurate data collection:
Prior to us presenting an Investigator for study participation, we assess the patient population from which study subjects will be drawn to assure the increased likelihood of enrollment goals being met. We firmly believe that the site must have the patient population or internal referral base from which to enroll patients.
Provide effective communication:
The success of a clinical investigation is based on ongoing support and communication between all parties. Since our commitment is the successful outcome of every study in which we participate, an internal staff is assigned to each study to ensure that communication is maintained and that the study receives the full attention it deserves until completion

Medical Service That You Can Trust

ABOUT US

Welcome to Prolific

QUALITY RESOURCING

QUALITY RESOURCING

EXPERIENCED CONSULTANTS

SOLUTION DEFINING

Who We Are

Who We Are

contact us