What is this?
TrialDocs collect and long term archive your clinical trial Site documents and coordinate the return of these upon any request. At the conclusion of the specified retention period, TrialDocs support you by contacting the product proprietor to gain green-light approval for secure destruction.
Currently, many Sites continue retaining archive sets, past the retention period, due to the hassle of chasing the proprietor for such an approval, at a great ongoing expense to Sites.
Advantage to you!
TrialDocs manages the complete process for you, from archive container provision, through to secure destruction after proprietor approval.
We provide you routine updates of your archive status. Site management will have confidence that the trial documentation is retained appropriately and is not bleeding their budgets, since documents will not be retained for longer than required.
One of the reasons why Biopharmaceutical companies are sending their Site project work to TrialDocs is to ensure that they maintain the required firewall between themselves and the Site documentation.
Where to get started?