FREQUENTLY ASKED QUESTIONS
Welcome to the CliniFluent FAQs page. Here, we have provided answers to some commonly asked questions about our services and programs.
CliniFluent is a clinical research training and services provider that caters to the needs of the pharmaceutical, biotech, and medical device industries. We offer various services such as capability development and training, clinical support services, and scientific events management.
We offer various training programs such as the Professional Diploma in Clinical Research (PDCR), Good Clinical Practice (GCP) training, and customized training programs for individuals and organizations.
The PDCR program is designed to be completed in 1 to 6 months, depending on the participant’s schedule and pace.
The PDCR program is open to individuals with a B.Pharm, M.Pharm, PhD, MBBS, MD, DNB, DM, BDS, MDS, BAMS, BHMS, BUMS, BPT, MPT, or life sciences degree (B.Sc, M.Sc, Biotechnology). Working professionals are also eligible to apply.
Evaluations in the PDCR program are based on assignments completed by the participants.
The cost of the PDCR program is affordable and competitive. Please refer to our Capability Development and Training page for more information.
We offer a range of clinical support services such as clinical trial monitoring, medical writing, data management, and statistical analysis.
At CliniFluent, we follow strict protocols to protect the confidentiality of client data. Please refer to our Privacy Policy page for more information.
You can contact us through the Contact Us page on our website or send an email to info@CliniFluent.com. Our team will get back to you as soon as possible.
