01
Name the patient
The surrogate, donor and intended parent may each be a separate patient or data subject for different services.
Patient rights and records guide
Identify the patient or data subject for each treatment and record. A commercial or family interest does not automatically create authority to consent for another person or access their health and genetic information.
Concise summary
Legal agreements, clinical decisions and informed consent perform different functions. Georgian patient-rights legislation addresses information, consent, medical records, confidentiality and privacy, while personal-data law gives health and genetic data special protection. For each procedure or disclosure, confirm who the patient is, who may lawfully act, what information was provided, which consent version applies and what limited records can be shared for the stated purpose.
01
The surrogate, donor and intended parent may each be a separate patient or data subject for different services.
02
A surrogacy contract does not replace procedure-specific informed consent or a clinician’s independent duties.
03
Share only what has a lawful basis, valid authority and necessary purpose, using secure channels.
The legal agreement may allocate responsibilities and record what participants intend, but a clinician determines the information and consent process required for medical care. Georgian patient-rights legislation addresses the patient’s right to information about proposed services, risks, alternatives and results, and requires informed consent before care, with written consent for specified services. The current provisions and clinical context should be checked.
Identify the patient for every step. An intended parent may be the patient for gamete collection or another procedure, a donor for retrieval, and a surrogate for transfer, pregnancy or delivery care. One participant’s contractual consent cannot be assumed to authorise another participant’s medical care. Emergency and representative situations require their own legal analysis.
The Patient Rights Law provides a framework for a patient, and in specified situations a relative or legal representative, to access and request copies of medical records. That does not mean intended parents automatically receive the surrogate’s or donor’s complete file. Ask who holds the record, who is the data subject, what authority exists and what limited information is necessary for treatment, legal evidence or another stated purpose.
Differentiate medical records from program reports. An agency update may summarise progress but is not necessarily the clinic’s official record. Intended parents should preserve their own clinical, contractual, consent and payment records and request corrections through the proper holder. If another participant authorises disclosure, the form should identify the records, recipient, purpose, duration and any lawful withdrawal process.
| Record | Likely data subject or holder | Question before disclosure |
|---|---|---|
| Intended parent’s procedure record | Patient and treating clinic | What access and copy process applies? |
| Surrogate pregnancy record | Surrogate patient and care provider | What lawful authority and necessary scope exist? |
| Donor screening or genetic data | Donor and relevant clinic or provider | What can be shared, and in what form? |
| Agency progress report | Agency under its contract and data duties | Is it accurate, sourced and within consent limits? |
Consent is not a one-time signature detached from later facts. When the proposed procedure, recipient, use of material, provider or disclosure changes, ask whether new information and consent are required. Record the date, version, explanation, signatories and clinician or provider responsible. Do not backdate a form or rely on an informal message where the law or provider requires a formal consent.
Contracts should explain who may issue non-medical instructions, but they should not pressure a patient to accept treatment or waive informed decision-making. If an intended parent, agency and clinic give inconsistent instructions, pause the administrative step where safe, identify the patient and competent decision-maker, preserve the messages and obtain clinical or legal advice as appropriate.
Georgia’s personal-data legislation treats health and genetic information as special-category data. Identify the lawful basis, purpose, minimum necessary content, recipients, security, retention and rights process for each disclosure. Use provider-to-provider secure exchange where appropriate instead of forwarding sensitive files through informal group chats or unnecessary intermediaries.
If records are missing, inaccurate or withheld, make a focused written request to the correct holder and state the authority and purpose. Preserve the request and response. Avoid threatening public disclosure or obtaining records through another person’s account. Counsel can assess access rights, contractual duties, evidence preservation and remedies, while urgent treatment information should be addressed promptly through the treating provider.
Decision framework
Apply the questions separately to each patient, data subject, procedure and disclosure.
The following primary sources informed this guide. Official English translations and service pages are useful orientation, but current Georgian text, implementing rules, authority practice and the particular facts should be checked before individual advice is given.
Related legal support
Move from general information to a review of the actual documents, participants and countries involved.
Review consent, records, confidentiality and storage terms in the clinical documents.
Explore this serviceMaintain independent document and consent oversight as circumstances change.
Explore this serviceAddress time-sensitive authority or record problems without substituting for care.
Explore this serviceContinue reading
Legal guide
Apply consent and privacy limits to donor documentation.
Read the guideLegal guide
Coordinate authority, data and custody across providers.
Read the guideLegal guide
Check final consents and instructions before treatment advances.
Read the guideClarify authority and access
Share the relevant agreements, consent forms, record request, participant roles and current deadline for a scoped legal assessment.