Clinical Trial Electronic Signature
Clinflash eSign
Standardizing the online document signatures and responding openly to all types of inspections


Expand patient enrollmentDigitized electronic signatures allow users to sign the process regardless of geographic and network environments, thereby accessing a broader, mobile patient base

Improve efficiency and reduce costsIt may improve the efficiency of clinical trials in all areas, accelerate the signing of documents, and save large annual costs on printing and mailing

Effective traceability and online verificationIt generates operation reports to facilitate effective traceability of product information, change records, rejection time, login information, and supports online verification of the authenticity of signed documents

Legitimate and compliantDigital technology helps to preserve complete electronic signature information, guaranteeing that the identity of the signing user is real and trustworthy, helping to make the processes of clinical trials transparent and reducing potential risks
Full compliance with Chinese and international regulations and guidelines1.Compliance with the regulations of FDA 21 CRF part 112.Developed in accordance with GAMP5 (system validation standards)
3.Complying with the latest GXP4.Complying with the Electronic Signature Law of the People's Republic of China
Full compliance with Chinese and international regulations and guidelines1.Compliance with the regulations of FDA 21 CRF part 112.Developed in accordance with GAMP5 (system validation standards)
3.Complying with the latest GXP4.Complying with the Electronic Signature Law of the People's Republic of China