{"product_id":"sop-on-sops","title":"SOP on SOPs","description":"\u003cp\u003e\u003cstrong\u003eThe foundational SOP that governs how all your other SOPs, Policies, Manuals, and Forms are created, numbered, reviewed, and maintained\u003c\/strong\u003e - the document control backbone of your Quality Management System.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eWho it's for:\u003c\/strong\u003e Virtual pharmaceutical sponsors setting up or standardizing their document control system across Policies, SOPs, Manuals, and Forms.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eWhat's included:\u003c\/strong\u003e\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003eDocument hierarchy (Manuals, Policies, SOPs, Forms) and numbering conventions\u003c\/li\u003e\n\u003cli\u003e16 governing Standards covering document ownership, review cycles, approval signatures, and periodic review timing\u003c\/li\u003e\n\u003cli\u003eFull procedure for creating, revising, and obsoleting documents, plus the review and approval workflow and periodic review process\u003c\/li\u003e\n\u003cli\u003eAppendix 1: Required Elements - header\/footer requirements and required sections by document type, in detailed reference tables\u003c\/li\u003e\n\u003cli\u003eAppendix 2: Document Numbering and Designations (department alpha codes, numbering scheme)\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003e\u003cstrong\u003eFormat:\u003c\/strong\u003e Fully editable Word document (.docx).\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eRegulatory alignment:\u003c\/strong\u003e References 21 CFR 211.22 (Responsibilities of the Quality Control Unit).\u003c\/p\u003e","brand":"FDA-SOPs","offers":[{"title":"Default Title","offer_id":52387113140529,"sku":null,"price":2500.0,"currency_code":"USD","in_stock":true}],"url":"https:\/\/www.fda-sops.com\/products\/sop-on-sops","provider":"FDA-SOPs","version":"1.0","type":"link"}