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Defines mandatory document sections (subject, purpose, scope, safety concerns, definitions, procedure, references, change history), formatting rules for headings, numbering, spacing, and required header and footer elements. Specifies issuance workflows for SOPs and associated forms, annual review and revision controls, training documentation, retrieval of superseded documents, and restrictions on unauthorized edits.",{"@graph":63,"@context":122},[64,80,101],{"@type":65,"itemListElement":66},"BreadcrumbList",[67,71,74,77],{"item":68,"name":69,"@type":70,"position":9},"https://docshare.wps.com","Home","ListItem",{"item":72,"name":10,"@type":70,"position":73},"https://docshare.wps.com/template/",2,{"item":75,"name":46,"@type":70,"position":76},"https://docshare.wps.com/template/paper-templates/",3,{"item":78,"name":59,"@type":70,"position":79},"https://docshare.wps.com/template/some-example-laboratory-working-procedure-standard-operating-procedures/246909/",4,{"url":78,"name":59,"@type":81,"image":82,"author":87,"headline":59,"publisher":90,"fileFormat":93,"inLanguage":57,"description":61,"dateModified":94,"datePublished":95,"encodingFormat":93,"isAccessibleForFree":96,"interactionStatistic":97},"DigitalDocument",{"url":83,"@type":84,"width":85,"height":86},"https://docshare.wps.com/thumbnails/some-example-laboratory-working-procedure-standard-operating-procedures/246909.png","ImageObject",442,249,{"name":88,"@type":89},"Aurelia","Person",{"url":68,"name":91,"@type":92},"DocShare","Organization","application/pdf","2026-10-05","2026-09-12",true,{"@type":98,"interactionType":99,"userInteractionCount":79},"InteractionCounter",{"@type":100},"ViewAction",{"@type":102,"mainEntity":103},"FAQPage",[104,110,114,118],{"name":105,"@type":106,"acceptedAnswer":107},"What is the purpose of the SOP writing and revision procedure?","Question",{"text":108,"@type":109},"It describes the steps and principles needed to write and revise standard operating procedures and their associated forms for compliance.","Answer",{"name":111,"@type":106,"acceptedAnswer":112},"What headings and section formatting rules must be followed?",{"text":113,"@type":109},"Use the specified font and map headings with X.0, X.X, and X.X.X to Heading 1, Heading 2, and Heading 3, with defined numbering and spacing rules.",{"name":115,"@type":106,"acceptedAnswer":116},"What information must be included in the SOP header and footer?",{"text":117,"@type":109},"The header must contain six specific items including title, unique procedure number, revision, effective date, and page numbering; the footer must include the stated verification phrase in Arial 8.",{"name":119,"@type":106,"acceptedAnswer":120},"How are SOPs and associated forms issued and revised under document control?",{"text":121,"@type":109},"Drafts are reviewed at draft stage and by the cGMP coordinator, electronic satisfactory drafts are provided to document control, sequential revisions are assigned, annual reviews are performed, significant quality-impact changes are introduced promptly, and outdated versions are replaced within a defined timeframe.","https://schema.org",{"og:url":78,"og:type":124,"og:title":59,"og:site_name":91,"og:description":61},"article",{"robots":126,"canonical":78},"index,follow",{"doc_id":128,"site_id":56},246909,1790240151,{"code":4,"msg":5,"data":131},{"doc_id":128,"user_id":132,"nickname":88,"user_avatar":133,"doc_module":9,"category_id":45,"category_name":46,"doc_title":59,"doc_description":61,"doc_content":134,"file_id":135,"file_url":136,"file_type":137,"file_size":138,"view_count":79,"is_deleted":4,"is_public":9,"is_downloadable":9,"audit_status":9,"page_count":139,"language":140,"language_code":57,"site_id":56,"html_lang":57,"table_of_contents":141,"faqs":142,"seo_title":143,"seo_description":61,"update_tm":144,"read_time":73},1099514068365,"https://ap-avatar.wpscdn.com/avatar/10000253d8d9f28188e?_k=1776742907772140068","Some Example Laboratory  \nWorking Procedure  \nAuthor: Someone Smith  \nReviewed and Approved By:  \nDATE  \n1.0 Subject  \nWriting Standard Operating Procedures.  \n2.0 Purpose  \nThe purpose of this procedure is to describe the steps and principles required to write and revise a standard operating procedures and associated forms.  \n3.0 Scope  \nThe scope of this procedure applies to the cGMP PET Program in the Medical Department including the GMP operations in the radiochemistry laboratory.  \n4.0 Safety Concerns  \nAny particular concerns that are relevant to the subject procedure even if such items are covered in a general safety manual, Experimental Safety Reviews (ESR) or Radiological Work Permits (RWP) .  \n5.0 Definitions  \nThe definition of all terms that are crucial for the understanding and correct performance of the procedure need to be included.  \n6.0 Procedure  \nAll procedure should be written according to the following instructions in order to be in compliance with GMP laboratory requirements. The standard font is Arial 12. Headings with X.0 should be classified as Heading 1. Headings with X.X should beset to Heading 2 and Headings with X.X.X should be set to Heading 3.  \n6.1 Template  \nUse the SOP template when writing procedures to ensure that all procedures meet minimum standards.  \n6.2 Printing  \nPrint all standard operating procedures on plain white 81/2 x 11 inch paper.  \n6.3 Header Information  \nInclude the following six pieces of information in the header:  \n1. Sample Hot Lab Standard Operating Procedure  \n2. Title stating the title of the SOP  \n3. Unique Procedure number assigned by Document Control made up of a letter and three numbers  \n4. Revision assigned by Document Control  \n5. Effective Date (DDMONXXXX) assigned by Document Control which is the date the SOP can be used  \n6. Page \\# of \\#  \n6.4 Procedure Body  \nInclude the following information in the body of the procedure. If the section doesn’t require any information, the SOP preparer should insert “n/a”.  \n1.0 Subject  \n2.0 Purpose  \n3.0 Scope  \n4.0 Safety Concerns  \n5.0 Definitions  \n6.0 Procedure  \n7.0 References  \n8.0 Change History  \n6.5 Numbering  \nNumber each section and subordinate headings decimally e.g. 6.0, 6. 1, 6.1. 1, 6.1.1.1 , etc.  \n6.5.1 Spacing  \nPlace two spaces after each number and before the heading text.  \n6.5.2 Section Separation  \nEnter a line before each X.X heading.  \n6.6 Procedure Inclusions  \nInclude Safety Concerns, Notes, and Handling and Packaging Requirements  \n6.6.1 Safety  \nInclude safety concerns if equipments relates to safety.  \n6.6.2 Packaging  \nInclude special handling/packaging requirements.  \n6.6.3 Notes  \nInclude Notes for special instructions.  \n6.7 Meaning of terms  \nUse certain verbs in these procedures which have the same meaning as their use in the cGMP regulation.  \n6.7.1 Mandatory requirements  \n“Must” or “Shall” indicate a mandatory requirement.  \n6.7.2 Desirable practice  \n“Should” or “May” indicate a desirable practice, but is not mandatory.  \n6.8 Footer Information  \nThe footer should contain the phrase:  \nVERIFY IN DOCUMENT CONTROL THAT THE REVISION IN THE HEADER IS STILL THE CURRENT VERSION.  \nIn Arial font 8  \n6.9 Issuance of SOPs and Forms  \nSOPs and associated forms should be written by a person competent and experienced to do so. It is accepted that the best person to write the SOP is the person who performs the procedure regularly. The Document Control Coordinator or designee will number and issue all SOPs and forms to the staff; and will also be responsible for organizing the annual review of SOPs and forms. The procedure for issuing SOPs (and forms) will be as follows:  \n• Each SOP/Form should be reviewed at draft stage by the staff that will use it to identify the issues addressed.  \n• The cGMP Coordinator or designee should review each SOP/Form.  \n• An electronic copy of the satisfactory draft SOP/Form should be provided to the Document Control Coordinator or designee. All other paper and el","cbCaiuoQnGBm8TDj","https://ap.wps.com/l/cbCaiuoQnGBm8TDj","pdf",48972,6,"English","# 1.0 Subject\n# 2.0 Purpose\n# 3.0 Scope\n# 4.0 Safety Concerns\n# 5.0 Definitions\n# 6.0 Procedure\n## 6.1 Template\n## 6.2 Printing\n## 6.3 Header Information\n## 6.4 Procedure Body\n## 6.5 Numbering\n## 6.6 Procedure Inclusions\n## 6.7 Meaning of terms\n## 6.8 Footer Information\n## 6.9 Issuance of SOPs and Forms\n## 6.10 Revision of SOPs/Forms\n## 6.11 Retrieval of SOPs/Forms","[{\"question\":\"What is the purpose of the SOP writing and revision procedure?\",\"answer\":\"It describes the steps and principles needed to write and revise standard operating procedures and their associated forms for compliance.\"},{\"question\":\"What headings and section formatting rules must be followed?\",\"answer\":\"Use the specified font and map headings with X.0, X.X, and X.X.X to Heading 1, Heading 2, and Heading 3, with defined numbering and spacing rules.\"},{\"question\":\"What information must be included in the SOP header and footer?\",\"answer\":\"The header must contain six specific items including title, unique procedure number, revision, effective date, and page numbering; the footer must include the stated verification phrase in Arial 8.\"},{\"question\":\"How are SOPs and associated forms issued and revised under document control?\",\"answer\":\"Drafts are reviewed at draft stage and by the cGMP coordinator, electronic satisfactory drafts are provided to document control, sequential revisions are assigned, annual reviews are performed, significant quality-impact changes are introduced promptly, and outdated versions are replaced within a defined timeframe.\"}]","Some Example Laboratory - Working Procedure - Standard Operating Procedures | PDF",1789238903]