System Implementation Agreement
Comprehensive agreement for implementing telemedicine systems and e-health platforms.
✓ SLA and KPIs ✓ Payment schedule ✓ Acceptance protocols
Download template (.docx)
Legal Support and Contract Templates
Comprehensive legal support for healthcare digitalisation projects. Contract templates, consultations and compliance assistance.
Contract Template Library
GDPR Data Processing Agreement
GDPR-compliant template for medical data (Art. 28 GDPR).
✓ Technical safeguards ✓ Sub-processors ✓ Audits
Download template (.docx)
Patient Consents
Package of consent templates for data processing and telemedicine.
✓ GDPR consent ✓ Telemedicine consent ✓ Patient information
Download package (.zip)
Advisory Services Agreement
Template agreement for healthcare advisory services.
✓ Scope of services ✓ Reporting ✓ IP and confidentiality
Download template (.docx)
IT Services SLA
Service Level Agreement for IT systems in medicine.
✓ 99.9% uptime ✓ 24/7 support ✓ Contractual penalties
Download template (.docx)
NDA and Confidentiality
Non-disclosure agreements for medical projects.
✓ Medical confidentiality ✓ Sensitive data ✓ IP protection
Download template (.docx)
Online Legal Consultations
Our lawyers specialise in medical law, GDPR in healthcare and public procurement.
Medical Law
- NFZ contracts
- Medical liability
- Industry regulations
- Licences and permits
GDPR and Data Protection
- GDPR compliance in healthcare
- Special category data (Art. 9)
- Security audits
- Incidents and breaches
Public Procurement
- Specification preparation
- Tender procedures
- Appeals and protests
- Framework agreements
Frequently Asked Legal Questions
Yes, informed patient consent is required. Consent should cover processing of medical data (Art. 9 GDPR) and provision of telemedicine services. A consent template is available in our library.
Under the Patient Rights Act – at least 20 years from the end of the year in which the last entry was made (or 30 years for records related to infectious diseases).
Yes, provided appropriate technical and organisational safeguards are in place, a data processing agreement is signed with the provider (Art. 28 GDPR) and requirements for sensitive data are met.
Systems must comply with GDPR, the Patient Rights Act, MDR regulation (if they are medical devices) and technical standards (ISO 27001, HL7 FHIR for integration).