Resources for Life Sciences Organisations

Explore some of our blogs, webinars, case studies and practical resources tailored to the key data protection challenges faced by Life Sciences organisations.

LIFE SCIENCES PLAYBOOK

A GDPR compliance guide for clinical trials, covering key areas of data protection:

Lawful bases for processing
Contracts and agreements
International data transfers
GDPR checklist

Download playbook

CASE STUDIES

Scaling EU research?
See how a US-based company tackled complex data flows to achieve success with EU study expansion.

Read case study

Struggling with EU data duties?
Learn how PCCTC streamlined compliance and met Article 27 obligations across borders.

Read case study

BLOGS

Data protection considerations for Clinical Trial Agreements

Clinical trials and vendor data processing agreements

GDPR considerations for Informed Consent Forms

CJEU clarifies pseudonymisation: What the EDPS v SRB ruling means for organisations

Clinical trials and GDPR: Overcoming common misconceptions

Comparison of privacy compliance and assurance in clinical trials and why both matter

WATCH ON DEMAND WEBINARS

NOT A CURE-ALL: Is tokenisation the solution for data sharing?

FULLY ASSURED: Getting privacy and assurance right in clinical trials

DOUBLE BLIND: Secondary use of health data and AI in clinical trials

STRICTLY CONFIDENTIAL: Reducing risk in Healthcare DSAR responses

FIRST, DO NO HARM: Safeguarding clinical trials from data breaches and legal challenges

UPCOMING EVENTS

The DPO Centre’s Life Sciences newsletter is a quick monthly read with useful information, articles, and views from our team of experienced DPOs on the latest data protection news specific to Life Sciences.

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