Pharmaceutical R&D
Supports governed pharmaceutical research workflows referencing GxP, FDA 21 CFR Part 11, ICH GCP, and HIPAA with protected-data redaction, an RBAC configuration point, source checks, quality scoring, a configurable human-oversight point, and audit capture.
This template is a configurable starting point and control mapping. It is not certification, legal advice, or a guarantee of compliance; validate it against your obligations and environment before use.
US, EU, Global
4 references
5 mapped domains
Regulated SaaS, Clinical Zero-Retention
Referenced Frameworks, Standards & Obligations
Mapped Control Domains
Deployment profiles
Get started in 3 steps
Open the template
Open the catalog entry in the Keeptrusts console and review its included controls, references, and deployment metadata.
Adapt the configuration
Use the template as a starting point, then adjust relevant policies, thresholds, routing, and review settings for your requirements.
Validate before rollout
Test every outcome you configure—such as allow, redact, block, or operator review—before deploying through a supported gateway workflow.
More Healthcare & Life Sciences templates
Clinical Decision Support
Clinical decision-support controls for PHI, citation checks, a configurable human-oversight point, and audit evidence.
Telehealth
Telehealth controls for PHI, an RBAC configuration point, citation checks, and a configurable human-oversight point.
Medical Records Summarization
Medical-summary controls for PHI, citation checks, a configurable human-oversight point, and traceability.