Patient rights and records guide

Medical Records and Informed Consent in IVF and Surrogacy

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.

Published: 4 August 2026Updated: 4 August 2026Last reviewed: 4 August 202612 minute read

Concise summary

What this guide helps you decide

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

Name the patient

The surrogate, donor and intended parent may each be a separate patient or data subject for different services.

02

Separate consent layers

A surrogacy contract does not replace procedure-specific informed consent or a clinician’s independent duties.

03

Limit record access

Share only what has a lawful basis, valid authority and necessary purpose, using secure channels.

Identify who can obtain which records

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-access analysis
RecordLikely data subject or holderQuestion before disclosure
Intended parent’s procedure recordPatient and treating clinicWhat access and copy process applies?
Surrogate pregnancy recordSurrogate patient and care providerWhat lawful authority and necessary scope exist?
Donor screening or genetic dataDonor and relevant clinic or providerWhat can be shared, and in what form?
Agency progress reportAgency under its contract and data dutiesIs it accurate, sourced and within consent limits?

Document changes and instructions

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.

  • Use version numbers or dates for every material consent form.
  • Confirm identity and signing authority.
  • Keep clinical explanation separate from commercial pressure.
  • Record lawful withdrawal or refusal and its contractual consequences separately.
  • Reconcile storage, donor and transfer instructions before use.

Protect privacy and prepare for record disputes

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.

Record request fields

  • requesting person and verified authority;
  • specific record and date range;
  • purpose and preferred secure delivery;
  • correction or explanation requested;
  • deadline linked to a genuine clinical or authority dependency.

Decision framework

Consent and records checklist

Apply the questions separately to each patient, data subject, procedure and disclosure.

Consent

  • Patient and decision-maker identified
  • Information, risks and alternatives handled clinically
  • Current written version where required
  • Change, refusal and withdrawal pathways

Records

  • Authoritative holder identified
  • Lawful access or representative authority
  • Necessary scope and correction process
  • Complete copy and version control

Privacy

  • Lawful basis and stated purpose
  • Special-category safeguards
  • Secure recipients and transfer
  • Retention and dispute record

Official sources and legal limits

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.

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