Getting Started

Learn the basics and set up your organization

• Platform onboarding guide
• Setting up roles and permissions
• Creating your first document
• Navigating the dashboard

QMS Workflows

Detailed guides for each QMS module

• Document control and approvals
• CAPA management
• Audit planning and execution
• Deviation tracking
• Training record management

AI Features

How to use CHARSTAN intelligence tools

• AI Assistant — how it works
• Automated gap analysis
• Smart document recommendations
• Predictive risk scoring

Compliance & Standards

Understand how CHARSTAN supports regulatory compliance

• ISO 13485 alignment
• FDA 21 CFR Part 11 compliance
• EU GMP Annex 11 readiness
• Audit trails and data integrity

Account & Organization

Manage your account, team, and settings

• Managing team members
• Configuring SSO and authentication
• Data retention policy
• Exporting your organization data

Troubleshooting

Solutions for common issues

• Login and session issues
• Document upload errors
• Data sync problems
• Browser compatibility