Pharma logistics and GDP compliance

Yes. Scilife helps organizations meet EU Good Distribution Practice guidelines for healthcare logistics and distribution. The platform supports controlled documentation, audit trails, role-based access, and traceability, helping logistics organizations demonstrate Good Distribution Practice compliance during audits and inspections.

Scilife standardizes documentation, training, deviations, CAPA, and change control across sites, making GDP compliance easier to manage as operations scale. Centralized oversight and logistics quality management reduce reliance on spreadsheets and local workarounds while maintaining consistent control.

Document control ensures procedures are current, consistently available, and traceable across all locations. Poor document control increases audit findings, delays inspections, and makes it difficult to demonstrate control over distribution activities.

Yes. While spreadsheets and shared drives may work initially, they become difficult to control as operations grow. A GDP-aligned eQMS provides version control, approvals, audit trails, and training linkage. All capabilities required to demonstrate compliance during inspections.

Scilife supports GDP audits by keeping documentation, training records, deviations, and change history centralized and inspection-ready. This allows teams to retrieve evidence quickly, respond confidently to auditor questions, and avoid last-minute preparation.

Yes. Scilife supports core Good Distribution Practice workflows, including Deviations, CAPAs, Change Control, Document Management, and Training. These workflows are designed to maintain traceability and consistency across sites, helping organizations identify recurring issues and demonstrate control.

Absolutely. Scilife is designed to support multi-site and multi-regional logistics operations, enabling centralized oversight while allowing local teams to operate efficiently. This is particularly important for organizations managing Good Distribution Practice compliance across warehouses, regions, or partners.

Scilife centralizes training records and links them directly to controlled procedures. This ensures staff are trained on the correct versions of documents and makes training evidence easy to demonstrate during inspections.

Scilife provides a guided, low-effort onboarding process tailored to healthcare logistics organizations. Most customers go live within 90 days, depending on scope, while continuing day-to-day operations without major disruption.

Yes. Scilife supports migration from legacy QMS tools, spreadsheets, shared drives, and partially digital systems. Our team guides customers through data extraction, formatting, and upload to ensure continuity and traceability during the transition.

Inconsistent documentation across sites makes it difficult to demonstrate control during audits and increases the risk of findings. A centralized QMS helps ensure procedures, training, and records remain aligned, reducing inspection risk as operations scale.