December 28, 2018 / NEWS
TFDA announcement: the due date of application for amendment replied document is changed to 14 days and implemented from July 1, 2019
November 13, 2018 / NEWS
TFDA entrust 35 intitutions to review the informed consent form that used in clinical trials from 06Nov2018 to 31Dec2020.
August 21, 2018 / NEWS
TFDA-The monitoring management and processing principle for custom clearance of Lab kit imports in the drug clinical trials
August 20, 2018 / NEWS
Implementation of the Enhanced Domestic Bioequivalence Study Inspection since January 1, 2018 by TFDA
Do-Intelligent Consulting Inc. is a professional Site Management Organization (SMO) that has established in June 2018. Chairman
Our study team possess over 15 years of experience in the clinical trial field and the Professional team members also possess a lot of experience in Phase I-IV studies and BA/BE studies over the years.
We can provide the full service of clinical trials to the study sites, biotechnology, pharmaceutical and contract research organization (CRO) companies.