In clinical trial processes, every trial phase includes various steps, decisions, and results. To do it right, all these need to be inked, approved, filed and submitted to appropriate parties. MSB Docs is easing it out particularly with the expansion of electronic and digital signatures. Book a demo to know-how.
In addition to getting every document signed and approved during each trial, there are other challenges too:
storing detailed records of each document transaction during trial.
patient recruitment and retention process.
data spread across too many disparate data sources.
MSB Docs Key Features:
Electronic & Digital Signature
Reduction in average time to sign clinical trials document
Approx. savings in paper-related costs in the first year of paperless clinical trials
Every technology that undergirds e-signature or digital signatures must adhere to international, published standards. MSB Docs – smart document solution is amongst those solutions that are fully compliant with federal Electronic Signatures in Global and National Commerce Act (ESIGN), the state-level Uniform Electronic Transactions Act (UETA), and 21 CFR Part 11 regulations outlined by U.S. Food and Drug Administration (FDA).