Electronic document management system with pharmaceutical document control and compliance
AmpleLogic's electronic document management system is a pharmaceutical document management software purpose-built for regulated industries. This compliance document management system features controlled SOP management, document approval workflow software, AI-powered indexing, and regulatory-ready audit trails. Manage SOPs, policies, and controlled documents with document version control software, electronic signatures, and automated distribution.
keyFeatures
Document version control software with automatic versioning, full history tracking and comparison capabilities.
21 CFR Part 11 compliant document management system with e-signatures and multi-level approval workflows.
Document lifecycle management software to manage documents from drafting through review, approval, distribution, and retirement.
Standardized templates for SOPs, policies, and controlled documents.
Automated reminders for periodic document reviews with configurable intervals.
Automatic training assignment when new or revised documents are published.
benefits
complianceStandards
useCases
ctaDescription
Streamline lab operations with a unified data management platform
StabilityEnterprise stability study management software for pharma shelf-life determination and regulatory compliance
QC PlanningIntelligent planning and campaign-based execution for QC laboratories
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