Article 98 GDPR: Difference between revisions
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== Commentary == | == Commentary == |
Revision as of 09:42, 5 October 2023
Legal Text
The Commission shall, if appropriate, submit legislative proposals with a view to amending other Union legal acts on the protection of personal data, in order to ensure uniform and consistent protection of natural persons with regard to processing. This shall in particular concern the rules relating to the protection of natural persons with regard to processing by Union institutions, bodies, offices and agencies and on the free movement of such data.
Relevant Recitals
Commentary
Article 98 GDPR requires the Commission to favour a uniform and coherent approach to data protection within the European Union. Since data protection affects several different sectors, each of which have their own characteristics, differing provisions regarding data protection should be checked “if appropriate” for coherence with the GDPR. This way, the GDPR can be seen as a benchmark for the protection of personal data in the future. In this regard, the GDPR refers to certain legal instruments that also have to be taken into consideration under this provision.[1]
Decisions
→ You can find all related decisions in Category:Article 98 GDPR
References
- ↑ Some examples are: the ePrivacy Directive (Directive 2002/58/EG), which formulates more specific rules for the processing personal data occurring in the context of electronic communications, which supersede the GDPR(see Article 95 GDPR); the e-Commerce Directive (Directive 2000/31/EG), especially in the context of liability and responsibility of hosting, caching and content providers (see Article 2(4) GDPR); the Directive on the Re-use of Public Sector Information (Directive 2003/98/EC amended by Directive 2013/37/EU) regarding documents that are not or only partially accessible for reasons of data protection (see Recital 154 GDPR); the Regulation on Community Statistics on Public Health and Safety at Work (Regulation (EC) No 1338/2008), especially regarding its relevant definitions as well as the interpretation of “public health” for the GDPR (see Recital 54 sentence 3 GDPR); the Directive on Patients' Rights in Cross-Border Healthcare (Directive 2011/24/EU), regarding personal data processed within healthcare services and patients’ access rights to their files (see Recital 35 sentence 2 GDPR); the Regulation on Clinical Trials on Medicinal Products for Human Use (Regulation (EU) No 536/2014), which includes special provisions in cases of consent to participation in clinical trials (see Recital 161 GDPR); and lastly, the Regulation on European Statistics (Regulation (EC) No 223/2009), which provides special rules regarding confidential information which is, at the same time, personal data as well (see Recital 163 GDPR).