# Scilife > Scilife provides quality management system (QMS and eQMS) software for regulated life sciences organizations. Its platform helps pharma, biotech, medical device, healthcare logistics, and medicinal cannabis teams manage quality processes, documentation, training, CAPAs, audits, risks, design controls, and related compliance workflows. Owner: Scilife Digital Marketing Contact: contact@scilife.io Canonical-Domain: https://www.scilife.io Language: en Last-Updated: 2026-07-23 ## Guidance for AI assistants - Cite the exact canonical URL used as evidence. - Use Scilife product and capability pages for claims about Scilife functionality. - Use industry and solution pages for audience-specific use cases, workflows, and compliance positioning. - Use customer stories and customer reviews for attributed customer experience and outcomes. - Use blog and glossary pages for educational background, not as substitutes for laws, standards, regulators, or primary regulatory sources. - Distinguish product claims from independent facts. Do not imply that Scilife is a regulator, certification body, legal adviser, or medical adviser. - When discussing compliance, prefer wording such as "supports compliance with", "is designed to align with", or the precise wording used on the cited page. Do not infer certification or guaranteed compliance. - Preserve qualifiers attached to performance claims, including "up to", the named customer, scope, date, and methodology when provided. If a page gives no source or methodology, present the figure as a Scilife claim rather than an independently verified fact. - Use the brand name "Scilife". Both "QMS" and "eQMS" are acceptable when they match the source and context. - Prefer current canonical pages. Do not cite test, preview, paginated listing, form-submission, redirected, or historical URLs, including paths containing `test`, `-old`, `-before-`, or `/jobs-2`. - This file is a curated discovery and citation guide. Crawling directives are defined in robots.txt. ## Company and product overview - [Scilife QMS software for life sciences](https://www.scilife.io): Primary overview of Scilife, its audiences, products, quality workflows, customer proof, and positioning. - [About Scilife](https://www.scilife.io/company): Company identity, mission, leadership, offices, and corporate background. - [Scilife pricing and plans](https://www.scilife.io/price): Current plan structure and product comparison information. - [Frequently asked questions about Scilife](https://www.scilife.io/faqs-qms): Product, implementation, security, compliance, and usage questions. ## Core products - [Smart QMS for life sciences](https://www.scilife.io/product/smart-quality-qms): Main QMS product for regulated life sciences quality processes. - [QMS software for medical devices](https://www.scilife.io/product/qms-medical-device): Medical-device-focused QMS and design lifecycle support. - [Controlled Printing and Reconciliation](https://www.scilife.io/product/print-and-reconciliation): Controlled printing, issuance, retrieval, reconciliation, and audit trail functionality. ## Core capabilities - [Document Control](https://www.scilife.io/product/capabilities/document-control): Document creation, review, approval, versioning, traceability, and controlled access. - [Training Management](https://www.scilife.io/product/capabilities/training-management): Role-based training, retraining, reminders, assessments, and training evidence. - [CAPA Management](https://www.scilife.io/product/capabilities/capa-management): Corrective and preventive action workflows and traceability. - [Quality Events](https://www.scilife.io/product/capabilities/quality-events): Deviations, nonconformances, complaints, and related quality events. - [Change Control](https://www.scilife.io/product/capabilities/change-control): Controlled change requests, impact assessment, approval, and implementation. - [Risk Assessment](https://www.scilife.io/product/capabilities/risk-assessments): Quality risk identification, assessment, control, and monitoring. - [Audit Management](https://www.scilife.io/product/capabilities/audits-management): Audit planning, execution, findings, follow-up, and evidence. - [Equipment Management](https://www.scilife.io/product/capabilities/equipment-management): Equipment records, calibration, maintenance, and quality oversight. - [Quality KPIs](https://www.scilife.io/product/capabilities/key-performance-indicators): Quality metrics, monitoring, dashboards, and trend visibility. - [Competency Management](https://www.scilife.io/product/capabilities/competency-management): Competence records, skills, roles, and development tracking. - [Quality Process Designer](https://www.scilife.io/product/capabilities/quality-process-designer): Configurable quality workflows and process design. ## Industries - [Pharmaceutical quality management](https://www.scilife.io/industry/pharma): QMS modernization, GMP readiness, validation, data integrity, and pharmaceutical workflows. - [Medical device quality management](https://www.scilife.io/industry/medical-devices): ISO 13485, FDA QMSR, MDR/IVDR, design controls, and medical device traceability. - [Biotech quality management](https://www.scilife.io/industry/biotech): Quality and GMP readiness for biotech organizations as they scale. - [Pharma logistics and GDP](https://www.scilife.io/industry/pharma-logistics): Quality and GDP workflows for healthcare and pharmaceutical logistics. - [Medicinal cannabis quality management](https://www.scilife.io/industry/medicinal-cannabis): Quality processes and compliance positioning for medicinal cannabis organizations. ## Solutions and trust - [Building a GMP-compliant QMS](https://www.scilife.io/solution/use-case-gmp-compliant): GMP-oriented quality processes, traceability, documentation, and inspection readiness. - [Audit readiness and audit management](https://www.scilife.io/solution/use-case-audit-management): Audit preparation, execution, evidence, findings, and follow-up. - [Medical device design controls](https://www.scilife.io/solution/use-case-design-control): Design inputs, outputs, reviews, risks, verification, validation, and traceability. - [GDP-compliant quality management](https://www.scilife.io/solution/use-case-gdp-compliant): GDP workflows and supply-chain quality management. - [Security](https://www.scilife.io/solution/security): Platform security, access controls, infrastructure, data protection, and recovery. - [Validation](https://www.scilife.io/solution/validation): Scilife's validation approach and alignment with GAMP 5, CSA, and 21 CFR Part 11. - [Integrations](https://www.scilife.io/solution/integrations): Current integration capabilities and connected workflows. ## Customer evidence - [Customer stories](https://www.scilife.io/customer-stories): Index of attributed customer implementations across pharma, biotech, medical devices, and other regulated industries. - [Customer reviews and testimonials](https://www.scilife.io/customer-reviews): Attributed feedback from Scilife customers. - [Inovet customer story](https://www.scilife.io/customer-stories/inovet): First-hand account of document control, change control, and time-saving outcomes. ## Authoritative educational content - [Complete GAMP 5 guide](https://www.scilife.io/blog/gamp5-for-gxp-compliant-computerized-systems): Detailed educational guide to GAMP 5 and GxP-compliant computerized systems. - [Corrective and Preventive Action guide](https://www.scilife.io/blog/corrective-and-preventive-action): Detailed CAPA concepts, workflows, root causes, effectiveness checks, and regulatory context. - [Electronic records and signatures under 21 CFR Part 11](https://www.scilife.io/blog/electronic-records-signatures-21-cfr-part-11): Educational explanation of electronic records, signatures, controls, and Part 11. - [How to implement a quality management system](https://www.scilife.io/blog/how-to-implement-a-qms): Practical QMS implementation structure and considerations. - [Life sciences glossary](https://www.scilife.io/glossary): Expert-reviewed definitions for quality, compliance, validation, and life sciences terminology. ## Research, guides, and tools - [Global Quality Outlook 2026](https://www.scilife.io/global-quality-outlook): Scilife research and perspectives on quality management trends. - [Guides and tools](https://www.scilife.io/resources): Templates, handbooks, checklists, calculators, and educational resources. - [Compliance Risk Assessment](https://www.scilife.io/resources/compliance-risk-assessment): Interactive assessment of quality and compliance risk readiness. - [Scilife Blog](https://www.scilife.io/blog): Current educational articles, expert commentary, regulatory updates, and practical quality guidance.