Trial Master File
Trial Master File
With the help of our Trial Master File feature, you can individually automate your master files and save valuable time in your day-to-day business while increasing inspection readiness.
Create your master file and link your maintained documents to the relevant sections of the master file. In the case of a trial master file (TMF), Docuply already offers the CDISC TMF reference model (formerly DIA). This eliminates the hassle of creating folder and subfolder structures on network drives or remote storage. Once linked, new, verified document versions are automatically attached to the relevant TMF, without any manual effort. This is how you can conveniently automate your TMF and other master files.
The overview of your master file can also be shared with external parties. To do this, simply invite your external partner and grant access rights to the TMF. Afterwards, it is possible to conveniently navigate through the individual zones and sections.
- Sharing master files with auditors, inspectors and other third parties
- Increased inspection readiness with less maintenance effort
- No surcharge on top of our pricing model
The following features will be available in the future:
- Site Master File (SMF)
- Drug Master File (DMF)
- Pharmacovigilance System Master File (PSMF)
- ZIP and PDF export possible at any time
Experience our smooth document management and fast automation of Trial Master Files for yourself without any obligation. Our 14-day trial period is free of charge and no payment method is required.
Testimonials
What experts say about us
"Docuply takes the stress out of audits and inspections by keeping everything in one place. It simplifies things for pharmaceutical teams and allows them to focus on what matters. Having seen how time-consuming and anxiety-inducing traditional audit preparation can be, I’m excited to support a tool that brings simplicity, transparency and real peace of mind to compliance."
