Decentralized Clinical Trials (DCT) & Hybrid Solutions

Clinical Development

Decentralized Clinical Trials (DCTs)

Customer-Centric and Globally Adaptive DCT Solutions.

Delivering a Wide Range of Virtual and Hybrid Approaches to Decentralized Clinical Trials

We offer flexible solutions for digital and decentralized trials in clinical development. Our DCT solutions leverage in-house expertise, including eConsent, TeleVisit, Direct-to-Patient Supply, etc., as well as cutting-edge technologies such as RBQM, eCPM, and ePay. These comprehensive solutions guide you through the planning, operation, and delivery of decentralized clinical trials. Our experience includes over 300 clinical trials using a DCT hybrid model, spanning the full research spectrum of indications, including oncology, vaccines, infectious diseases, and more.

300+

Clinical trials incorporate elements of DCT

40%+

Tigermed's on-going clinical trials incorporating DCT elements

Tigermed DCT Platform

Out-of-hospital Solutions

IRT/DTP

Enhance subjects’ adherence, drug traceability and study blinding controls.

ePRO/eDiary

Enhance subjects compliance, data quality, and efficiency.

ePAY

Reduce subjects' financial burden with timely payments, assurance of a secured payment system, and fair compensation.

DHT/Digital Medicine

Improve the efficiency of clinical trials.

CTRM & RBQM

Enhance study quality and cost savings

In-hospital Solutions

E2E

Enhances data quality and governance efficiency, expedites progress, and reduce costs.

SEDS

Remote review of participants qualification which significantly improve enrollment timeline.

eCOA

Enhance data compliance and quality.

TeleVisit

Facilitates communication between Principal Investigators (PIs) and subjects.

eConsent

Empowers subjects to make fully informed decisions.

Tigermed DCT Complete Map

An Intelligent, Integrated System That Meets Both Patient Needs and Regulatory Requirements

Tigermed's decentralized trial platform is built around the participant. It provides technology and service solutions for every step of a participant’s journey through a clinical trial, reducing the burden of taking part and making participation more convenient and friendly, so that participants can join a trial comfortably and with peace of mind.

Unifying Connections for Improved Data Quality and Enhanced Patient Experiences

Decentralization

A digital trial that facilitates participant access, diminishing the significance of their geographical location or workplace.

Participant Centricity

Digital trials aim to enhance the participant experience, simplifying the process for individuals to join and successfully complete a trial.

Efficiency

Through digitization and process simplification, digital trials aim to decrease trial duration and costs, and promote higher rates of trial completion.

Interoperability

Digital trials are enabled by a direct exchange of information between systems.

Practical Application

Registered Clinical trials
Post-market research
RWS
Investigator-initiated research

Therapeutic Areas

Neurology, respiratory, endocrinology, oncology, pediatrics, Covid-19 and others.

Success Stories

In a COVID-19 neutralizing antibody trial, 3,500 participants were recruited within 10 days using e-recruitment and e-Consent
In an MRCT focusing on migraine, data from more than 1,000 participants were collected using ePRO, significantly improving data quality and efficiency.
A cost reduction of more than 30% was achieved through the utilization of a remote and hybrid model in multiple Phase III trials.