CSV for GxP Systems - EU-GMP & FDA 21 CFR Part 11 compliance

CSV for GxP Systems - EU-GMP & FDA 21 CFR Part 11 compliance yra paremtas OYTEC

“OYTEC” savo žmogiškojo kapitalo patirtį ir žinias teikiame klientų aptarnavimui, siūlydami geriausią sprendimą, atitinkantį verslo tikslus: norą užmegzti glaudžius ir ilgalaikius partnerių santykius su klientais, pagrįstus abipusiu pasitikėjimu, bendru darbu ir paslaugų meistriškumu. Atsižvelgiant į žmogiškąjį kapitalą kaip diferencinį elementą. Sistemos bus kuriamos ir kuriamos taip, kad padėtų žmonėms ir skatintų jų kūrybiškumą. Siūlome sprendimus specializacijos prielaida kaip mūsų patirties ir žinių pagrindu. Daugiausia GMP ir FDA Compliance aplinkoje.

Atraskite OYTEC

Kodėl Risk-based CSV services for GxP computerized systems?

Empower your pharmaceutical operations with absolute regulatory confidence. OYTEC transforms your validation strategy into a competitive advantage, delivering audit-ready GxP systems. By integrating GAMP 5 excellence into your lifecycle, we ensure your technology drives production forward without compliance friction. Secure your Go-Live with precision-engineered documentation and expert partnership for any global platform.

Scientist in protective gear using laptop

Privalumai

Inspection-ready evidence:
Audit-ready validation deliverables aligned to EU-GMP and FDA 21 CFR Part 11, structured for fast review and clear traceability from requirements to testing.
Faster & safer go-live:
Risk-based CSV (GAMP® 5 aligned) focuses effort where it matters most, reducing rework and enabling confident release to production without delaying the project.
Applicable to any GxP system:
Proven methodology adaptable to any computerized system (manufacturing, quality, lab, or enterprise), including Siemens Opcenter Execution Pharma and integrated landscapes.
Quality as a Business Driver:
Validation embedded into lifecycle governance (change, periodic review, incident handling) to maintain a controlled state and prevent compliance drift over time, turning quality into a tool for continuous process improvement.
Complete Data Integrity.
Our validation protocols rigorously verify ALCOA+ principles throughout your system’s lifecycle. Assuring integrity, safety and trceability of all GxP data.

Pagrindinės Funkcijos

Strategic Validation Planning

We define the roadmap for compliance success. From the Validation Master Plan (VMP) to detailed risk assessments, we establish a clear, structured framework that aligns project stakeholders and sets the standard for quality deliverables from day one.

Scientists in protective gear in laboratory

Risk-Based Verification

Optimise testing efforts with precision. Using GAMP® 5 risk assessment methodologies (FMEA), we identify critical process flows, configurations, integrations and developements. This focuses verification on high-risk areas, ensuring patient safety without over-testing.

Data Integrity Assurance

Safeguarding your digital records. We execute specific protocols to verify ALCOA+ compliance, ensuring your system’s security, audit trails, and electronic signatures meet FDA 21 CFR Part 11 and EU Annex 11 requirements for total data reliability.

Scientist in clean room operating equipment

Lifecycle Quality Management

Quality integrated at every step. We manage the entire V-model lifecycle (URS, FS, DS, IQ, OQ, PQ) ensuring traceability between requirements and tests. Our approach guarantees that quality is built into the design, preventing costly errors during final qualification.