{"product_id":"document-review","title":"Fixed-Scope Document Review: Up to 5 Adapted Templates","description":"\u003ch2\u003eWhat you get\u003c\/h2\u003e\u003cul\u003e\n\u003cli\u003eA review of \u003cstrong\u003eup to 5 documents\u003c\/strong\u003e you have adapted from our ISO 9001:2026 or ISO 13485 templates (or your own documents for the same standards): procedures, the quality manual, forms or registers. A document is one procedure, manual, form or register, up to 25 pages.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eWritten feedback within 5 business days\u003c\/strong\u003e of receiving all files: comments in the documents themselves plus a one-page summary that ranks findings by audit risk (likely nonconformity, observation, improvement).\u003c\/li\u003e\n\u003cli\u003eEach comment references the clause it relates to and says what to change, not just what is wrong.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eOne re-review\u003c\/strong\u003e of the revised documents within 30 days, with written confirmation of what is now closed.\u003c\/li\u003e\n\u003cli\u003eAn optional 30-minute video call to walk through the feedback.\u003c\/li\u003e\n\u003c\/ul\u003e\u003ch2\u003eWhat it checks\u003c\/h2\u003e\u003cul\u003e\n\u003cli\u003eDoes each document cover what the clause requires for your scope?\u003c\/li\u003e\n\u003cli\u003eDo the procedures, forms and records link up (no orphan forms, no records the procedure never mentions)?\u003c\/li\u003e\n\u003cli\u003eAre template placeholders, example text and inapplicable sections removed or justified?\u003c\/li\u003e\n\u003cli\u003eIs it consistent with your quality manual, scope and organization?\u003c\/li\u003e\n\u003cli\u003eWould an auditor be able to follow the evidence trail?\u003c\/li\u003e\n\u003c\/ul\u003e\u003ch2\u003eWhat it does not include\u003c\/h2\u003e\u003cul\u003e\n\u003cli\u003eWriting or rewriting documents for you (that is \u003ca href=\"\/pages\/consulting\"\u003econsulting\u003c\/a\u003e).\u003c\/li\u003e\n\u003cli\u003eDevice-specific technical content such as test methods, biocompatibility or clinical evaluation.\u003c\/li\u003e\n\u003cli\u003eLegal advice, or any guarantee of a certification or audit outcome.\u003c\/li\u003e\n\u003cli\u003eDocuments for other standards (ISO 42001, SOC 2, CMMC) unless agreed in writing first.\u003c\/li\u003e\n\u003c\/ul\u003e\u003ch2\u003eHow it works\u003c\/h2\u003e\u003col\u003e\n\u003cli\u003eBuy the review. You get an email within one business day asking for your documents and a short description of your company and scope.\u003c\/li\u003e\n\u003cli\u003eSend the files (Word preferred, PDF accepted). Confidential? We sign your NDA first.\u003c\/li\u003e\n\u003cli\u003eReceive the commented documents and summary within 5 business days.\u003c\/li\u003e\n\u003cli\u003eRevise, send back within 30 days, and get the re-review.\u003c\/li\u003e\n\u003c\/ol\u003e\u003ch2\u003eWho reviews\u003c\/h2\u003e\u003cp\u003eIshan Maharaj, Founder and Principal Consultant (BSc Engineering (Honours) Industrial, MSc Engineering Management), who writes and maintains the templates. See \u003ca href=\"\/pages\/how-we-review-templates\"\u003ehow we review templates\u003c\/a\u003e.\u003c\/p\u003e\u003ch2\u003eRefunds\u003c\/h2\u003e\u003cp\u003eIf we cannot start within 10 business days of your order, or you cancel before sending documents, you get a full refund. Once feedback is delivered the fee is not refundable. See the \u003ca href=\"\/policies\/refund-policy\"\u003erefund policy\u003c\/a\u003e.\u003c\/p\u003e","brand":"ISO Cloud Consulting","offers":[{"title":"Default Title","offer_id":67873947910338,"sku":"ICC-ONBOARD-60","price":349.0,"currency_code":"USD","in_stock":true}],"url":"https:\/\/isocloudconsulting.com\/products\/document-review","provider":"ISO Cloud Consulting","version":"1.0","type":"link"}