CEE&DACH Expert Webinar | 28th of September | Register now for free
Protect intellectual property. Ensure easier partnering with other companies.
Share documentation of several R&D projects in one place
Conduct out-licensing and in-licensing faster
Streamline communication between clinical advisory board and investors
Develop pharmaceutical products within medical areas with total information control
Protect intellectual property with the ISO 27001 and GDPR certified tool
Increase the chance of a quick and successful Clinical Decision Making
Easy and secure communication between the R&D department, regulatory agencies and patients in clinical trials.
Launch Virtual Data Room when you need it (framework agreement) or use the subscription and increase the efficiency and safety of work of many departments in your organization.
Buy a self-service version of VDR Lite and optimize audit costs or opt for the VDR Basic version (good for M&A) and enjoy full FORDATA 24/7 support.
Negotiate individual legal and financial terms once and launch VDRs by email when you need them. Pay only when the Virtual Data Room is running.
Create a central, protected document repository in the cloud with multiple levels of access for many departments (R&D, Regulatory Affairs, Licensing, IP, IT). Implement many projects independently in one system.
“Virtual Data Room allowed us to share confidential source documents with external entities. It has greatly facilitated the work of project managers who efficiently exchanged confidential information with each other and helped to divide the work on the project.”
“RTA VC Sp. z o. o. SKA decided to use the FORDATA VDR service due to the need for efficient organization of the Due Diligence survey, which was carried out by our consultants. Thanks to cooperation with FORDATA we have gained much more than just a secure platform for exchanging confidential documents. FORDATA took comprehensive care of the preparation and coordination of the entire process.”