Industry Use Case
DPDP compliance for Pharma & Life Sciences
Clinical trial data, pharmacovigilance records, and HCP engagement data create unique DPDP obligations. Discovery+ maps consent across trial phases, enforces retention for regulatory submissions, and documents cross-border data transfers.
Clinical trial participant consent lifecycle
Clinical trial participants provide consent for specific research purposes. Discovery+ maps this consent across trial phases, flags data used beyond the consented purpose, and enforces deletion when the trial concludes.
Pharmacovigilance personal data governance
Pharmacovigilance data includes sensitive personal data from adverse event reports. Discovery+ classifies this data, enforces retention for regulatory submissions, and documents the legal basis for processing.
HCP engagement data documentation
Healthcare professional engagement data — including contact details, specialisation, and interaction history — must be processed with a valid consent or legitimate interest basis. Discovery+ maps and documents this data estate.
Cross-border transfer documentation for global trials
Global clinical trials transfer personal data across borders. Discovery+ maps every cross-border flow, documents the transfer mechanism, and flags transfers to countries not yet notified by the Central Government.
Regulatory submission data retention enforcement
Regulatory submissions require personal data to be retained for defined periods. Discovery+ enforces these retention periods, prevents premature deletion, and triggers archival workflows when the period expires.
Patient support programme data governance
Patient support programmes collect sensitive personal data including health information and financial details. Discovery+ maps the consent basis, enforces purpose limitation, and automates deletion when the programme ends.
See Discovery+ for Pharma & Life Sciences
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