Advisory Notice and FSCA — Process Package (ISO 13485)
€69.00Advisory Notice / FSCA SOP with FSCA Decision Worksheet and Field Safety Notice (FSN) per MDCG 2024-1.
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Advisory Notice / FSCA SOP with FSCA Decision Worksheet and Field Safety Notice (FSN) per MDCG 2024-1.

CAPA SOP with comprehensive CAPA Template covering full lifecycle: Initiation, Triage, Root Cause Analysis, Action Planning, Implementation, Effectiveness Verification.

Process Package — Corrective and Preventive Action (CAPA) A complete CAPA system covering ISO 13485:2016 §8.5.2–8.5.3, MDSAP Chapter 1–2, and FDA QMSR expectations. CAPA is the most-cited finding area in regulatory audits — this package addresses it head-on with a lifecycle-complete template and a procedure that integrates risk-based prioritization. What’s included: SOP-CORE-04 CAPA — full…

Change Control SOP with comprehensive Change Form including MDCG 2020-3 substantial change assessment matrix.

Clinical Evaluation SOP with CEP and CER templates. Aligned with EU MDR Annex XIV + MDCG 2020-5 (equivalence) + MDCG 2020-13 (CEAR).

Complaint Management SOP with Complaint File template that INTEGRATES the 4-question Reportability Assessment per Art. 87.

Complete ISO 13485 QMS Documentation Kit — All 30 Process Packages + Quality Manual + Master Tracker. Aligned with ISO 13485:2016, EU MDR 2017/745, FDA QMSR, and MDSAP.

Computer System Validation SOP with Validation Plan & Report and IQ/OQ/PQ Protocol templates. Aligned with GAMP 5 and 21 CFR Part 11.

Customer-Related Processes SOP with Customer Order / Contract Review Form (per ISO 13485 §7.2.2).

Design and Development Control SOP with 6 templates: Plan, I/O Matrix (Excel), Review Record, Verification, Validation, Transfer Checklist. Largest package in the kit.

Audit-ready Document Control SOP plus 3 templates: Master List, Change Request Form, and Record Destruction Authorization. Aligned with ISO 13485:2016 §4.2 and 21 CFR Part 11.

Process Package — Document and Record Control A complete, audit-ready document control system covering all requirements of ISO 13485:2016 §4.2.4–4.2.5, MDSAP Chapter 1, and 21 CFR Part 11 for electronic records. What’s included: SOP-CORE-01 Document and Record Control — full standard operating procedure with cover page, control page, responsibilities matrix, document hierarchy, lifecycle workflow, periodic…

EU Vigilance Reporting SOP with PSUR template (per MDCG 2022-21). Covers Art. 87-92 reporting timelines and EUDAMED submission.

HR + Training SOP with Job Description (PRRC role), Training Plan & Record (Excel), and Competence Matrix (16 pre-populated competences).

Incoming Inspection SOP with Inspection Plan & Report (Excel) and CoA/CoC Review Record. AQL sampling per ANSI/ASQ Z1.4.

Infrastructure & Equipment Control SOP with Equipment Master List (Excel — auto-calc Days Until Cal) and Maintenance & Calibration Record.
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