Legal

GDPR Statement

Effective Date: February 2026

Document Version: 1.0

1. Overview

Rymeda, Inc. (“Rymeda,” “we,” “us”) is a Delaware corporation headquartered in California that operates a HIPAA-compliant healthcare SaaS platform providing electronic health records (EHR), telehealth, clinical AI (ORIS), voice-to-note transcription, secure messaging, and a healthcare marketplace. Although Rymeda is a US-based entity, we are committed to complying with the General Data Protection Regulation (EU) 2016/679 (“GDPR”) whenever it applies to our processing activities.

This statement describes how Rymeda aligns its data protection practices with GDPR requirements, the rights available to data subjects in the European Economic Area (EEA) and United Kingdom, and the safeguards we maintain for international data transfers. This statement supplements our Privacy Policy and Data Processing Agreement.

2. Scope & Applicability

The GDPR applies to Rymeda's processing activities when:

  • We process personal data of individuals located in the EU/EEA in connection with offering our platform services to them (Article 3(2)(a)).
  • We monitor the behavior of individuals within the EU/EEA, such as through analytics or usage tracking (Article 3(2)(b)).
  • A customer (controller) established in the EU/EEA engages Rymeda as a data processor under our Data Processing Agreement (Article 28).

Where Rymeda acts as a processor on behalf of a healthcare organization (controller), the controller determines the purposes and means of processing, and Rymeda processes personal data solely on documented instructions. Where Rymeda acts as a controller — for example, when managing provider accounts or website visitors — we comply directly with all applicable GDPR obligations.

3. Legal Basis for Processing

Rymeda relies on the following legal bases under GDPR Article 6 (and Article 9 for special categories of data) depending on the processing activity:

Legal BasisGDPR ArticlePlatform Use
ConsentArt. 6(1)(a), Art. 9(2)(a)Voice recording for transcription, AI-generated clinical notes (ORIS), telehealth session recording, marketing communications
Contract PerformanceArt. 6(1)(b)Account creation, EHR service delivery, telehealth appointments, billing and invoicing, marketplace transactions
Legitimate InterestArt. 6(1)(f)Platform security, fraud detection, service improvement, cookie-free analytics (Plausible), secure messaging delivery
Legal ObligationArt. 6(1)(c)HIPAA compliance, clinical record retention, audit logging, tax and financial reporting, breach notification
Vital InterestsArt. 6(1)(d), Art. 9(2)(c)Emergency clinical situations where processing is necessary to protect a patient's life or health

Special Category Data: Health data, biometric data (voice recordings), and AI-derived clinical data are processed under Article 9(2)(a) (explicit consent), Article 9(2)(h) (healthcare provision), or Article 9(2)(c) (vital interests) as applicable. All AI-generated clinical content requires clinician review and signature before becoming part of the medical record.

4. Data Subject Rights (Articles 15–22)

Rymeda supports and facilitates the exercise of all GDPR data subject rights. Requests may be submitted to legal@rymeda.com and will be fulfilled within 30 days.

RightArticleImplementation
Right of AccessArt. 15Full data export in machine-readable JSON including profile, posts, comments, messages, login history, sessions, bookings, community memberships, and provider data
Right to RectificationArt. 16Update personal data via platform settings or upon written request; changes are logged in the immutable audit trail
Right to ErasureArt. 17Profile anonymization (email replaced with deleted_{id}@deleted.rymeda.com, name set to “Deleted User”), soft-deletion of posts and comments (content replaced with “[Deleted]”), session invalidation, and audit log anonymization
Right to RestrictionArt. 18Processing restricted upon request while accuracy disputes or objections are resolved; restricted data is marked and active processing ceases
Right to Data PortabilityArt. 20Structured JSON export of all user data, downloadable via authenticated API endpoint with a 7-day expiration window
Right to ObjectArt. 21Cease processing based on legitimate interest upon request; immediate opt-out from non-essential communications
Automated Decision-MakingArt. 22All AI-generated clinical content (ORIS suggestions, transcriptions, SOAP notes, ICD-10 codes) requires human clinician review and provider signature — no solely automated decisions with legal or significant effect

Erasure & Retention: The right to erasure is subject to legal retention obligations. Clinical records governed by HIPAA (45 CFR §164.530(j)) must be retained for six years. Where erasure conflicts with retention requirements, data is anonymized rather than deleted, and processing is restricted to the retention purpose only. Audit logs may be preserved in anonymized form (actor email replaced with the anonymized address) to maintain system integrity.

5. Data Protection Principles (Article 5)

Rymeda adheres to the core data protection principles set out in GDPR Article 5:

Lawfulness, Fairness & Transparency

We process personal data only with a valid legal basis, provide clear privacy notices, and maintain an AI Transparency policy disclosing how clinical AI systems operate.

Purpose Limitation

Personal data is collected for specified, explicit, and legitimate purposes — healthcare delivery, platform operation, billing, and compliance — and not further processed in a manner incompatible with those purposes.

Data Minimization

We collect only the personal data necessary for each processing purpose. Our PHI redaction pipeline strips identifiable health information before data reaches external AI processing layers. Website analytics use Plausible (cookie-free, no PII).

Accuracy

We provide tools for data subjects and controllers to keep personal data accurate and up to date, including NPI/NPPES validation for provider credentials and patient self-service profile management.

Storage Limitation

Personal data is retained only as long as necessary for its processing purpose or as required by law. Our Data Retention Policy documents specific retention periods for each data category.

Integrity & Confidentiality

We implement AES-256 encryption at rest (per-tenant AWS KMS keys), TLS 1.3 in transit, role-based access controls with a 9-role clinical permission matrix, immutable audit logging, tenant isolation, and VPC network security.

Accountability

Rymeda maintains records of processing activities (Article 30), conducts Data Protection Impact Assessments, undergoes annual SOC 2 Type II audits, and designates a Data Protection Officer contactable at legal@rymeda.com.

6. International Data Transfers

Rymeda's infrastructure is hosted in AWS US-East-1 (Northern Virginia). When personal data is transferred from the EEA, UK, or Switzerland to the United States, we rely on the following safeguards:

  • Standard Contractual Clauses (SCCs): Module Two (Controller to Processor) per EU Commission Implementing Decision (EU) 2021/914, incorporated into our DPA. UK International Data Transfer Addendum and Swiss FADP modifications apply where relevant.
  • HIPAA Safeguards: As a HIPAA-compliant platform, we maintain security standards that meet or exceed GDPR Article 32 requirements, including Business Associate Agreements with all subprocessors handling PHI.
  • Encryption: AES-256 encryption at rest with per-tenant AWS KMS keys and TLS 1.3 for all data in transit, ensuring data remains protected regardless of jurisdiction.
  • Transfer Impact Assessment: We have conducted a TIA confirming that our supplementary measures — including tenant isolation, per-tenant encryption keys, and strict access controls — provide an essentially equivalent level of protection for transferred personal data.

7. Data Protection Impact Assessments

Rymeda conducts Data Protection Impact Assessments (DPIAs) as required by GDPR Article 35 whenever processing is likely to result in a high risk to the rights and freedoms of individuals. We conduct DPIAs for:

  • AI processing of clinical data: ORIS clinical AI, AI-generated SOAP notes, and suggested ICD-10 codes with confidence scoring
  • Voice transcription: Recording and transcribing clinical encounters using OpenAI Whisper, involving biometric (voice) data
  • Telehealth services: Real-time audio/video consultations involving health data
  • New feature launches: Any new processing activity involving health data, biometric data, or large-scale profiling

Each DPIA includes: (a) a systematic description of processing operations and purposes; (b) an assessment of necessity and proportionality; (c) an evaluation of risks to data subjects; and (d) documented mitigation measures. We cooperate with controllers who must conduct their own DPIAs, providing technical documentation and processing details upon request.

8. Data Processor Obligations

When acting as a data processor under GDPR Article 28, Rymeda:

  • Processes personal data only on documented instructions from the controller
  • Ensures all personnel processing data are bound by confidentiality obligations
  • Implements appropriate technical and organizational security measures (Article 32)
  • Engages sub-processors only with prior authorization and equivalent contractual protections
  • Assists with data subject rights, breach notification, DPIAs, and prior consultation
  • Returns or deletes all personal data upon termination, subject to legal retention
  • Makes available all information necessary to demonstrate compliance and supports audits

A complete list of our sub-processors — including their purpose, data processed, and location — is maintained on the Subprocessor List page. All sub-processors handling health data are covered by Business Associate Agreements. Controllers receive 30 days' advance notice of sub-processor changes with a 15-day objection window.

9. Breach Notification

72-Hour Notification (Article 33): In the event of a personal data breach, Rymeda notifies the affected controller without undue delay and no later than 72 hours after becoming aware of the breach, providing the nature of the breach, approximate number of data subjects affected, likely consequences, and measures taken or proposed to mitigate the breach.

Where a breach is likely to result in a high risk to the rights and freedoms of individuals, we assist controllers in fulfilling their obligation to notify data subjects under Article 34. Breach notifications include: (a) the categories of data affected; (b) contact details of our Data Protection Officer; (c) a description of likely consequences; and (d) remediation measures.

For breaches involving Protected Health Information, HIPAA breach notification requirements under 45 CFR §§164.404–164.410 apply concurrently. See our Breach Notification Policy for full details.

10. Data Protection Officer

Rymeda has designated a Data Protection Officer (DPO) who can be reached for any GDPR-related inquiries, data subject requests, or complaints:

Data Protection Officer

legal@rymeda.com

Data subject requests, GDPR inquiries, DPIAs, privacy complaints

Legal Department

legal@rymeda.com

DPA amendments, SCC execution, regulatory correspondence

11. Supervisory Authority

Data subjects in the EU/EEA have the right to lodge a complaint with their local supervisory authority (data protection authority) if they believe their personal data is being processed in violation of the GDPR (Article 77). A list of EU supervisory authorities is available from the European Data Protection Board.

UK data subjects may contact the Information Commissioner's Office (ICO). Swiss data subjects may contact the Federal Data Protection and Information Commissioner (FDPIC).

We encourage data subjects to contact us at legal@rymeda.com before filing a complaint so that we may attempt to resolve the concern directly.

12. Related Policies