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Priority review Consultation Amended Consultation

Guidelines 1/2026 on Processing Personal Data for Scientific Research Purposes

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Summary

The European Data Protection Board has opened a public consultation on Guidelines 1/2026 addressing the processing of personal data for scientific research purposes under the GDPR. The guidelines cover topics including legal basis, consent requirements, and data subject rights in research contexts. Comments may be submitted until 25 June 2026, after which submitted responses will be published on the EDPB website.

Published by EDPB on edpb.europa.eu . Detected, standardized, and enriched by GovPing. Review our methodology and editorial standards .

What changed

The EDPB is consulting on updated guidelines that will clarify how GDPR provisions apply specifically to scientific research activities involving personal data processing. The consultation covers legal basis requirements, conditions for relying on consent or other grounds, and the interplay between research purposes and data subject rights. Research institutions, clinical investigators, healthcare entities conducting studies, and public health authorities will need to review the final guidelines to ensure their data processing activities comply with the updated interpretation. Organizations should consider submitting comments on any practical challenges or ambiguities they currently face in applying data protection rules to research data.

Affected parties including universities, hospitals, pharmaceutical companies, medical device manufacturers, and public health authorities conducting scientific research should monitor this consultation closely. The final guidelines will provide authoritative EDPB interpretation on key issues such as compatible use of research data, safeguards for secondary use, and the application of derogations under Article 89 GDPR. Early engagement during the consultation period allows stakeholders to shape the final guidance before it becomes the standard for assessing research data processing compliance across EU member states.

Archived snapshot

Apr 17, 2026

GovPing captured this document from the original source. If the source has since changed or been removed, this is the text as it existed at that time.

Start Date: 16 April 2026 End Date: 25 June 2026 Public consultation reference: 1/2026 Public consultation ongoing Guidelines 1/2026 669.4KB English Download Publication Type:
- Guidelines
Topics:
- Health
- Controller
- Processor
- Legal basis
- Consent
- Data subject rights
The European Data Protection Board welcomes comments on the *Guidelines 1/2026 on processing of personal data for scientific research purposes.*
Such comments should be sent *25th June 2026 at the latest
using the provided form.*

Please note that, by submitting your comments, you acknowledge that your comments will be published on the EDPB website.

The EDPB Secretariat staff screens all replies provided before publication (only for the purpose of blocking unauthorised submissions, such as spam), after which the replies are made available to the public directly on the EDPB public consultations’ page. Unauthorised submissions are immediately deleted. The attached files are not altered in any way by the EDPB.

Please note that your contribution may be subject to a request for access to documents under Regulation 1049/2001 on public access to European Parliament, Council and Commission documents. In this case the request will be assessed against the conditions set out in the Regulation and in accordance with applicable data protection rules.

All legal details can be found in our Specific Privacy Statement (SPS) .

Provide your feedback

Named provisions

Legal basis for processing Consent in research contexts Data subject rights Compatible use for research Article 89 safeguards

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Last updated

Classification

Agency
EDPB
Published
April 16th, 2026
Comment period closes
June 25th, 2026 (69 days)
Instrument
Consultation
Legal weight
Non-binding
Stage
Consultation
Change scope
Substantive
Document ID
EDPB Guidelines 1/2026
Docket
1/2026

Who this affects

Applies to
Clinical investigators Healthcare providers Public health authorities
Industry sector
6111 Higher Education 3254 Pharmaceutical Manufacturing 3345 Medical Device Manufacturing
Activity scope
Research data processing Clinical trial compliance Health data governance
Geographic scope
European Union EU

Taxonomy

Primary area
Data Privacy
Operational domain
Compliance
Compliance frameworks
GDPR
Topics
Healthcare Pharmaceuticals Medical Devices

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