ICH Good Clinical Practice
International standard for the design, conduct, and reporting of clinical trials involving human subjects.
Quick Facts
- Documents Included
- 14
- Category
- Healthcare & Life Sciences
- Regions
- Saudi Arabia / GCC European Union / UK United States
- Compliance Domains
- 5 domains
What's Included
SeedGovernance provides 14 ready-to-use templates for ICH GCP, covering 5 compliance domains. Each document is pre-filled with framework-specific guidance so you can start immediately.
Clinical Trials
Policies, processes, and evidence templates
Informed Consent
Policies, processes, and evidence templates
IRB/IEC
Policies, processes, and evidence templates
Investigator Responsibilities
Policies, processes, and evidence templates
Monitoring
Policies, processes, and evidence templates
How SeedGovernance Helps with ICH GCP
Beyond templates, our platform guides you through every step of ICH GCP compliance.
Assessment Wizard
Answer guided questions to assess your ICH GCP readiness and identify gaps.
Gap Analysis
Automatically surface what's missing from your ICH GCP compliance programme.
Document Library
14 pre-built templates tailored to ICH GCP requirements.
Operations Modules
Track incidents, changes, risks, and vendors — all mapped to ICH GCP controls.
KPI Dashboard
Monitor your ICH GCP compliance score in real time with automated metrics.
Auditor Access
Share a read-only view of your ICH GCP compliance status with auditors.
Related Frameworks in Healthcare & Life Sciences
Organizations using ICH GCP 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.
GxP
14 documents
Quality guidelines and regulations for life sciences covering GMP, GLP, GCP, and GDP.
ISO 13485
14 documents
Quality management system standard for organizations involved in medical device lifecycle.
Start your free trial with ICH GCP
Get instant access to 14 ICH GCP templates, guided assessments, and a complete compliance management platform. No credit card required.
14-day free trial · No credit card required · Cancel anytime