The subordinate SMO team under Titanium Pharmaceutical is a professional clinical trial site management organization (Site Management Organization, SMO), dedicated to assisting researchers and research institutions to undertake non-medical judgments and operational tasks in clinical trials through professional services related to clinical trials, improve the quality of clinical trials, accelerate the progress of clinical trials, and promote the standardization of clinical trials.

Subject recruitment

Subject screening

Assist in informed consent

Collection of medical history and general data of subjects before enrollment

Arrangements and records of physical examinations and special examinations

Arrangement, coordination and reporting of laboratory inspections

Checking and randomization of subjects' inclusion criteria

Collection, sorting and preservation of original data

AE/SAE collection, recording and reporting

Subject medication guidance

Assist in research on drug distribution, recovery, counting, preservation and recording

Assist laboratory sample management

CRF (electronic) entry and Q&A

Researcher work assistance and communication and coordination

Subject's education and communication

Subject follow-up arrangement and management

Subject compliance assessment

Query communication and give feedback based on the researcher's reply

Institutional/ethics document submission and communication and coordination

Reception and problem handling and feedback for supervision, check, verification and inspection

Study on material management

Update and management of study center folder