Tmfy streamlines the organization, tracking, and storage of all your clinical trial documents. With its user-friendly interface and full regulatory compliance, Tmfy redefines document management. Book a demo today and see for yourself!
Optimize your TMF management
Tmfy transforms document management by simplifying processes and allowing you to focus on what really matters: the success of your clinical research and improving patient outcomes.
Simplicity at your fingertips
In the fast-paced world of clinical research, having a tool that enhances efficiency and saves time is essential. Tmfy adapts to your needs, making document management straightforward and hassle-free.
Data traceability and integrity
Easily track and verify all processes and documents, ensuring full transparency. Traceability is key to staying compliant with regulatory standards and maintaining data integrity throughout the trial.
AI-Driven value for Clinical Trials
At Sermes CRO, we turn your needs into practical document management solutions. By automating tasks, we reduce manual work and eliminate human error, improving accuracy and efficiency.
Revolutionizing traditional Clinical Trial document management with full regulatory compliance
Tmfy ensures that all your documents are managed according to current regulations, removing the risks and delays associated with traditional document handling.
Tmfy provides a comprehensive solution that not only enhances document management but also optimizes resources, ensures regulatory compliance, and improves traceability—all in a streamlined, efficient way.
Tmfy provides a comprehensive solution that not only enhances document management but also optimizes resources, ensures regulatory compliance, and improves traceability—all in a streamlined, efficient way.
Responsible Party: Sermes Planificación SLU
Postal Address: C/ Rufino González 14, Esc.1ª-2ºD, 28037 Madrid (Spain)
Email of the Data Protection Officer: protecciondedatos@sermescro.com
Purpose:
To manage requests from interested parties, address their inquiries, and, if requested, send you our communications (such as a newsletter if requested by the interested party).
We will process your data for as long as necessary to attend to your request or inquiry.
For managing the newsletter, we will process your data until you unsubscribe or cancel your newsletter subscription.
Legitimacy:
Consent of the interested party.
Recipients:
The data will be shared with other companies in the group to which SERMES CRO belongs for internal administrative purposes. Sermes does not intend to process your personal data outside the European Economic Area.
Rights:
– Right to request access to the data.
– Right to request rectification or deletion.
– Right to request restriction of processing.
– Right to object to the processing.
– Right to data portability.
To exercise your rights, you can send an email to protecciondedatos@sermescro.com.
Additional Information:
You can consult the additional and detailed information on Data Protection at this link on our website.
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