Good Practice Regulations (GxP)
Quality guidelines and regulations for life sciences covering GMP, GLP, GCP, and GDP.
Quick Facts
- Documents Included
- 14
- Category
- Healthcare & Life Sciences
- Regions
- Saudi Arabia / GCC European Union / UK United States
- Compliance Domains
- 6 domains
What's Included
SeedGovernance provides 14 ready-to-use templates for GxP, covering 6 compliance domains. Each document is pre-filled with framework-specific guidance so you can start immediately.
GMP
Policies, processes, and evidence templates
GLP
Policies, processes, and evidence templates
GCP
Policies, processes, and evidence templates
GDP
Policies, processes, and evidence templates
Quality Management
Policies, processes, and evidence templates
Validation
Policies, processes, and evidence templates
How SeedGovernance Helps with GxP
Beyond templates, our platform guides you through every step of GxP compliance.
Assessment Wizard
Answer guided questions to assess your GxP readiness and identify gaps.
Gap Analysis
Automatically surface what's missing from your GxP compliance programme.
Document Library
14 pre-built templates tailored to GxP requirements.
Operations Modules
Track incidents, changes, risks, and vendors — all mapped to GxP controls.
KPI Dashboard
Monitor your GxP compliance score in real time with automated metrics.
Auditor Access
Share a read-only view of your GxP compliance status with auditors.
Related Frameworks in Healthcare & Life Sciences
Organizations using GxP often also need these frameworks.
HIPAA
37 documents
US federal law protecting sensitive patient health information from being disclosed without consent.
FDA
41 documents
FDA regulations on electronic records and signatures in pharmaceutical and medical device industries.
EU MDR
18 documents
EU regulation governing the production and distribution of medical devices in the European market.
MHRA
16 documents
UK Medicines and Healthcare products Regulatory Agency framework for medical devices and pharmaceuticals.
ICH GCP
14 documents
International standard for the design, conduct, and reporting of clinical trials involving human subjects.
ISO 13485
14 documents
Quality management system standard for organizations involved in medical device lifecycle.
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