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Document Management System

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

everythingYouNeed

Document Version Control

Document version control software with automatic versioning, full history tracking and comparison capabilities.

Electronic Signatures

21 CFR Part 11 compliant document management system with e-signatures and multi-level approval workflows.

Document Lifecycle Management

Document lifecycle management software to manage documents from drafting through review, approval, distribution, and retirement.

Template Management

Standardized templates for SOPs, policies, and controlled documents.

Periodic Review

Automated reminders for periodic document reviews with configurable intervals.

Training Integration

Automatic training assignment when new or revised documents are published.

benefits

whyChoose

Eliminate paper-based document control with digital document control system
Ensure only current versions are in use
Reduce document review cycles by 45%
Full traceability and audit readiness
Automated compliance workflows
Cloud document management software for pharma with secure access control

complianceStandards

builtForCompliance

USFDA 21 CFR Part 11EU Annex 11ISO 9001GMPMHRA

useCases

designedForWorkflows

Controlled SOP ManagementPolicy ControlBatch Record TemplatesRegulatory SubmissionsPrint Issuance and Retrieval

readyToTransform

ctaDescription

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