Showing 17–26 of 26 results
Process Package — Management Review Complete, audit-ready management review system covering ISO 13485:2016 §5.6 and MDSAP Chapter 1 expectations. Includes the 17 mandatory review inputs, output decisions framework, and integration with CAPA and KPI processes. What’s included: SOP-CORE-02 Management Review — full procedure with frequency, agenda structure, input checklist (all 17 ISO §5.6 inputs), output…
MDSAP Documentation Kit — Complete The flagship kit. Everything your QMS needs to face an MDSAP audit confidently across all 5 jurisdictions: Brazil, Japan, Canada, Australia, USA. 15 procedures + 18 templates + a User Guide and Master Index, all aligned to the latest 2025-2026 regulatory frameworks. What’s included: Shared Core (4 procedures + 8…
Audit-ready MDSAP Program Management SOP. The master document tying together all MDSAP processes across 5 jurisdictions (Brazil, Japan, Canada, Australia, USA).
Nonconformance Management SOP with NC Report template (severity classification, RCA, disposition).
Process Package — Marketing Authorization Japan (PMDA) Complete framework for Japanese PMDA medical device authorization. Covers DMAH designation, Foreign Manufacturer Registration (Form 63-5), JMDN code mapping, the three pathways (Todokede / Ninsho / Shonin), STED dossier, ICH E5 ethnic factor assessment, and tempu bunsho management. What’s included: SOP-REG-JP Marketing Authorization Japan — full procedure: MAH/DMAH…
Process Package — Vigilance Reporting Japan (PMDA) Complete framework for Japanese medical device vigilance under PMD Act Art. 68-10. Covers the LISTED vs UNLISTED logic (events already in tempu bunsho follow 30-day path; UNLISTED follow stricter 15-day path), causality assessment, mandatory PSB/PSD fax notification for deaths, and tempu bunsho management strategy. What’s included: SOP-VIG-JP Vigilance…
Purchase Management SOP with combined Purchase Specification + PO template (Part A specs + Part B PO).
Supplier Management SOP with Evaluation Form, Approved Supplier List (Excel), and bilateral Quality Agreement.
Process Package — Marketing Authorization Australia (TGA) Complete framework for Australian TGA ARTG inclusion. Covers Sponsor designation, classification under TG (MD) Regulations 2002, the five conformity assessment pathways, Essential Principles (Schedule 2), AusUDID (effective 2025), and Annual Reports for ARTG-included devices. What’s included: SOP-REG-AU Marketing Authorization Australia — full procedure: Sponsor designation, classification rules, 5…
Process Package — Vigilance Reporting Australia (TGA) Complete framework for Australian medical device incident reporting. Covers Medical Device Incident Report (MDIR) under TG (MD) Regulations 2002, the Australia-specific exemption mechanism (events that meet specific criteria can be aggregated in Annual Reports rather than reported individually), and the PRAC (Procedure for Recalls, Product Alerts and Product…
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