T-005-007 Technical Responsible designation
Designation
Configuration
The purpose of this document is to formally appoint a Technical Director in accordance with the requirements set forth in the Medical Device Regulation (EU) 2017/745.
To that end, we hereby appoint Full name of designee, with national identification number ID number, holding a degree in Degree and professional experience in the field, to said position. They will provide services exclusively to our company, allocating 100% of their time to this role.
Full name of designee | Ms. Aguilar Robles |
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Received and acknowledged | Certifies that the knowledge has been acquired |
Company Identifying Information
Property | Value |
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Company name | AI Labs Group, S.L. |
Trademark | Legit.Health ® |
ID Number | (ES)B95988127 |
Activity | Provision of clinical intelligence and communication software for HCP. |
Address | Gran Via, BAT Tower, 48001, Bilbao, Spain |
Telephone | +34 653 08 83 37 |
hello@legit.health | |
Website | https://legit.health |
Legal representative | Ms. Aguilar Robles |
Signature meaning
The signatures for the approval process of this document can be found in the verified commits at the repository for the QMS. As a reference, the team members who are expected to participate in this document and their roles in the approval process, as defined in Annex I Responsibility Matrix
of the GP-001
, are:
- Author: Team members involved
- Reviewer: JD-003, JD-004
- Approver: JD-001