Public Health Ethics

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General Data Protection Regulation (GDPR)

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Public Health Ethics

Definition

The General Data Protection Regulation (GDPR) is a comprehensive data protection law in the European Union that came into effect on May 25, 2018. It establishes strict guidelines for the collection and processing of personal information, aiming to enhance individual privacy rights and empower individuals regarding their personal data. The GDPR has significant implications for how organizations, including those in public health, manage and protect sensitive data, particularly when big data analytics are involved.

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5 Must Know Facts For Your Next Test

  1. GDPR applies to any organization that processes the personal data of EU citizens, regardless of the organization's location.
  2. One key aspect of GDPR is the requirement for organizations to obtain explicit consent from individuals before collecting or processing their personal data.
  3. Under GDPR, organizations must implement measures to ensure data protection by design and by default, incorporating privacy into their operations from the outset.
  4. Breach notification is mandatory under GDPR; organizations must report data breaches to authorities within 72 hours and inform affected individuals when necessary.
  5. Non-compliance with GDPR can result in hefty fines of up to €20 million or 4% of a company's global annual revenue, whichever is higher.

Review Questions

  • How does GDPR affect the way public health organizations collect and use big data?
    • GDPR imposes strict requirements on public health organizations regarding the collection and use of big data. These organizations must ensure that they have obtained explicit consent from individuals before processing their personal information. Additionally, they need to implement robust data protection measures and respect individual rights concerning their data. This regulation aims to build trust among individuals that their sensitive health information is handled responsibly.
  • Discuss the significance of obtaining explicit consent under GDPR in relation to public health research.
    • Obtaining explicit consent under GDPR is crucial for public health research as it ensures that individuals are aware of how their personal data will be used and processed. This requirement enhances transparency and accountability in research practices, allowing individuals to make informed decisions about participating in studies. It also safeguards against potential misuse of personal health data, promoting ethical standards in research while fostering trust between researchers and participants.
  • Evaluate the implications of GDPR for innovation in health technologies and big data analytics.
    • GDPR presents both challenges and opportunities for innovation in health technologies and big data analytics. On one hand, the stringent requirements for data protection and privacy can slow down the development and deployment of new technologies due to compliance complexities. On the other hand, by establishing clear guidelines for data handling and empowering individuals with rights over their information, GDPR encourages the creation of more secure and ethical health technologies. This dual impact may lead to innovative solutions that prioritize user privacy while still harnessing the power of big data for public health advancements.

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