{"id":334473,"date":"2024-10-19T23:19:21","date_gmt":"2024-10-19T23:19:21","guid":{"rendered":"https:\/\/pdfstandards.shop\/product\/uncategorized\/jcr-camlab-2021\/"},"modified":"2024-10-25T22:17:48","modified_gmt":"2024-10-25T22:17:48","slug":"jcr-camlab-2021","status":"publish","type":"product","link":"https:\/\/pdfstandards.shop\/product\/publishers\/joint-commission\/jcr-camlab-2021\/","title":{"rendered":"JCR CAMLAB 2021"},"content":{"rendered":"

Continuous compliance starts with staff who know what The Joint Commission requires. The 2021 Comprehensive Accreditation Manual for Laboratory and Point-of-Care Testing (CAMLAB) provides the key information your organization needs to power performance improvement and maintain continuous standards compliance. It features the official Joint Commission standards, National Patient Safety Goals, and other accreditation requirements. The portable CAMLAB is spiral bound with color-coded tabs that allow you to find exactly what you need for standards compliance or survey readiness when you need it. Inside you\u2019ll find descriptions of the survey and decision process, questions to prompt discussion in your organization about compliance with the standards, checklists of the elements of performance that require written documentation, and action planning worksheets to address any issues of noncompliance. It’s lean and light, making it a perfect on-the-go reference. Keep it handy in meetings, during orientation and training, and as a practical overview of the Joint Commission\u2019s accreditation requirements for everyone in your organization, from staff to leaders. Then, get ready to power performance improvement and excellence in your laboratory services! Please note: The CAMLAB is delivered annually. For the most up-to-date standards throughout 2021, access your E-dition on your Joint Commission ConnectTM extranet site or consider purchasing the E-dition Laboratory version. Key Topics: \u2022 “Gold tab” standards requirements including the standards, National Patient Safety Goals, and Accreditation Participation Requirements effective January 1, 2021 \u2022 “Blue tab” accreditation process information about Joint Commission policies and procedures and practical survey preparation information on the Early Survey Policy, documentation requirements, patient safety systems and more \u2022 Several appendixes, including one on standards related to Individualized Quality Control Plans (IQCP) and a new one on duplicated standards between the laboratory and hospital accreditation programs \u2022 Keys to successfully using the manual for survey preparedness Key Features: \u2022 Survey readiness tools including compliance prompts, documentation checklists, and action planning worksheets in every standards chapter \u2022 Icons to help navigate documentation requirements as well as risk areas \u2022 “What’s New” summary of changes made since the previous print edition Standards: All laboratory standards Setting: Organizations accredited under the Laboratory Accreditation Program, including \u2022 Laboratories in hospitals, clinics, nursing care facilities, home care organizations, behavioral health care organizations, ambulatory sites and physician offices \u2022 Reference laboratories \u2022 Freestanding laboratories, such as assisted reproductive technology laboratories \u2022 Blood transfusion and donor center laboratories \u2022 Public health laboratories, including Indian Health Service laboratories \u2022 Laboratories in federal health care facilities, such as the Department of Veterans Affairs \u2022 Point-of-care test sites in patient care areas, which may include blood gas laboratories providing services to patients in emergency rooms, surgical suites, and cardiac catheterization laboratories Key Audience: Staff responsible for accreditation, compliance, patient safety,<\/p>\n

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PDF Pages<\/th>\nPDF Title<\/th>\n<\/tr>\n
1<\/td>\nWhat\u2019s New 2021 CAMLAB <\/td>\n<\/tr>\n
13<\/td>\nCover <\/td>\n<\/tr>\n
14<\/td>\nThe Joint Commission Mission <\/td>\n<\/tr>\n
15<\/td>\nContents <\/td>\n<\/tr>\n
17<\/td>\nIntroduction: How The Joint Commission Can Help You Move Toward High Reliability (INTRO) <\/td>\n<\/tr>\n
18<\/td>\nI. Introduction to Joint Commission Accreditation <\/td>\n<\/tr>\n
22<\/td>\nII. About the <\/td>\n<\/tr>\n
34<\/td>\nIII. Steps to Achieving and Maintaining Compliance <\/td>\n<\/tr>\n
41<\/td>\nIV. Get Extra Help <\/td>\n<\/tr>\n
43<\/td>\nPatient Safety Systems (PS)
Introduction <\/td>\n<\/tr>\n
44<\/td>\nWhat Does This Chapter Contain? <\/td>\n<\/tr>\n
46<\/td>\nBecoming a Learning Organization <\/td>\n<\/tr>\n
47<\/td>\nThe Role of Laboratory Leaders in Patient Safety <\/td>\n<\/tr>\n
52<\/td>\nData Use and Reporting Systems <\/td>\n<\/tr>\n
56<\/td>\nA Proactive Approach to Preventing Harm <\/td>\n<\/tr>\n
59<\/td>\nEncouraging Patient Activation <\/td>\n<\/tr>\n
60<\/td>\nBeyond Accreditation: The Joint Commission Is Your Patient Safety Partner <\/td>\n<\/tr>\n
62<\/td>\nReferences <\/td>\n<\/tr>\n
64<\/td>\nAppendix. Key Patient Safety Requirements <\/td>\n<\/tr>\n
73<\/td>\nAccreditation Participation Requirements (APR)
Overview <\/td>\n<\/tr>\n
74<\/td>\nChapter Outline <\/td>\n<\/tr>\n
75<\/td>\nRequirements, Rationales, and Elements of Performance <\/td>\n<\/tr>\n
89<\/td>\nDocument and Process Control (DC)
Overview <\/td>\n<\/tr>\n
90<\/td>\nChapter Outline <\/td>\n<\/tr>\n
91<\/td>\nStandards, Rationales, and Elements of Performance <\/td>\n<\/tr>\n
113<\/td>\nEnvironment of Care (EC)
Overview <\/td>\n<\/tr>\n
116<\/td>\nChapter Outline <\/td>\n<\/tr>\n
117<\/td>\nStandards, Rationales, and Elements of Performance <\/td>\n<\/tr>\n
149<\/td>\nEmergency Management (EM)
Overview <\/td>\n<\/tr>\n
152<\/td>\nChapter Outline <\/td>\n<\/tr>\n
153<\/td>\nStandards, Rationales, and Elements of Performance <\/td>\n<\/tr>\n
175<\/td>\nHuman Resources (HR)
Overview <\/td>\n<\/tr>\n
177<\/td>\nChapter Outline <\/td>\n<\/tr>\n
178<\/td>\nStandards, Rationales, and Elements of Performance <\/td>\n<\/tr>\n
199<\/td>\nInfection Prevention and Control (IC)
Overview <\/td>\n<\/tr>\n
201<\/td>\nChapter Outline <\/td>\n<\/tr>\n
202<\/td>\nStandards, Rationales, and Elements of Performance <\/td>\n<\/tr>\n
219<\/td>\nInformation Management (IM)
Overview <\/td>\n<\/tr>\n
220<\/td>\nChapter Outline <\/td>\n<\/tr>\n
221<\/td>\nStandards, Rationales, and Elements of Performance <\/td>\n<\/tr>\n
235<\/td>\nLeadership (LD)
Overview <\/td>\n<\/tr>\n
238<\/td>\nChapter Outline <\/td>\n<\/tr>\n
239<\/td>\nStandards, Rationales, and Elements of Performance <\/td>\n<\/tr>\n
271<\/td>\nNational Patient Safety Goals (NPSG)
Chapter Outline <\/td>\n<\/tr>\n
272<\/td>\nRequirements, Rationales, and Elements of Performance <\/td>\n<\/tr>\n
279<\/td>\nPerformance Improvement (PI)
Overview <\/td>\n<\/tr>\n
281<\/td>\nChapter Outline <\/td>\n<\/tr>\n
282<\/td>\nStandards, Rationales, and Elements of Performance <\/td>\n<\/tr>\n
289<\/td>\nQuality System Assessment for Nonwaived Testing (QSA)
Overview <\/td>\n<\/tr>\n
290<\/td>\nChapter Outline <\/td>\n<\/tr>\n
295<\/td>\nStandards, Rationales, and Elements of Performance <\/td>\n<\/tr>\n
479<\/td>\nTransplant Safety (TS)
Overview <\/td>\n<\/tr>\n
480<\/td>\nChapter Outline <\/td>\n<\/tr>\n
481<\/td>\nStandards, Rationales, and Elements of Performance <\/td>\n<\/tr>\n
493<\/td>\nWaived Testing (WT)
Overview <\/td>\n<\/tr>\n
496<\/td>\nChapter Outline <\/td>\n<\/tr>\n
497<\/td>\nStandards, Rationales, and Elements of Performance <\/td>\n<\/tr>\n
511<\/td>\nThe Accreditation Process (ACC)
Notices
ACC Chapter Contents <\/td>\n<\/tr>\n
513<\/td>\nOverview <\/td>\n<\/tr>\n
514<\/td>\nAccreditation Policies <\/td>\n<\/tr>\n
536<\/td>\nBefore the Survey <\/td>\n<\/tr>\n
541<\/td>\nDuring the Survey <\/td>\n<\/tr>\n
554<\/td>\nAfter the Survey <\/td>\n<\/tr>\n
564<\/td>\nBetween Accreditation Surveys <\/td>\n<\/tr>\n
576<\/td>\nDecision Rules for Organizations Seeking Initial Accreditation <\/td>\n<\/tr>\n
579<\/td>\nDecision Rules for Organizations Seeking Reaccreditation <\/td>\n<\/tr>\n
583<\/td>\nProcess for Organizations That Meet Decision Rule PDA02 for Patients Placed at Risk for Serious Adverse Outcomes Due to Signific <\/td>\n<\/tr>\n
585<\/td>\nProcess for Organizations That Meet Decision Rule PDA04 <\/td>\n<\/tr>\n
586<\/td>\nReview and Appeal Procedures <\/td>\n<\/tr>\n
593<\/td>\nStandards Applicability Grid (SAG) <\/td>\n<\/tr>\n
659<\/td>\nSentinel Events (SE)
I. Sentinel Events <\/td>\n<\/tr>\n
663<\/td>\nII. Goals of the Sentinel Event Policy <\/td>\n<\/tr>\n
664<\/td>\nIII. Responding to Sentinel Events <\/td>\n<\/tr>\n
671<\/td>\nIV. The Sentinel Event Database
V. Determination That a Sentinel Event Is Subject to Review <\/td>\n<\/tr>\n
672<\/td>\nVI. Optional On-Site Review of a Sentinel Event
VII. Disclosable Information
VIII. The Joint Commission\u2019s Response <\/td>\n<\/tr>\n
673<\/td>\nIX. Sentinel Event Measures of Success (SE MOS)
X. Handling Sentinel Event\u2013Related Documents <\/td>\n<\/tr>\n
674<\/td>\nXI. Oversight of the Sentinel Event Policy
XII. Survey Process <\/td>\n<\/tr>\n
675<\/td>\nAppendix. Accreditation Requirements Related to Sentinel Events <\/td>\n<\/tr>\n
677<\/td>\nThe Joint Commission Quality Report (QR)
Introduction
What Is The Joint Commission Quality Report? <\/td>\n<\/tr>\n
678<\/td>\nWhat Will My Quality Report Contain?
What Is Quality Check? <\/td>\n<\/tr>\n
679<\/td>\nCan My Laboratory Comment on Its Quality Report? <\/td>\n<\/tr>\n
680<\/td>\nWhat Are the Marketing and Communication Guidelines for Publicizing Your Accreditation and Commitment to Quality? <\/td>\n<\/tr>\n
683<\/td>\nRequired Written Documentation (RWD) <\/td>\n<\/tr>\n
684<\/td>\nList of EPs Requiring Written Documentation for Laboratories and Pointof Care Testing <\/td>\n<\/tr>\n
689<\/td>\nEarly Survey Policy (ESP) <\/td>\n<\/tr>\n
695<\/td>\nAppendix A: Retention Times for Records, Reports, and Specimens (AXA)
Retention Times for Records, Reports, and Specimens <\/td>\n<\/tr>\n
699<\/td>\nAppendix B: Laboratory Developed Tests (AXB)
Laboratory Developed Tests <\/td>\n<\/tr>\n
701<\/td>\nAppendix C: Individualized Quality Control Plan\u2013Eligible Requirements (AXC) <\/td>\n<\/tr>\n
703<\/td>\nAppendix D: Duplicate Laboratory and Hospital\/ Critical Access Hospital Requirements (AXD) <\/td>\n<\/tr>\n
705<\/td>\nGlossary (GL) <\/td>\n<\/tr>\n
729<\/td>\nIndex (IX) <\/td>\n<\/tr>\n<\/table>\n","protected":false},"excerpt":{"rendered":"

Comprehensive Accreditation Manual for Laboratory and Point-of-Care Testing (CAMLAB)<\/b><\/p>\n\n\n\n\n
Published By<\/td>\nPublication Date<\/td>\nNumber of Pages<\/td>\n<\/tr>\n
Joint Commission<\/b><\/a><\/td>\n2021<\/td>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n","protected":false},"featured_media":334482,"template":"","meta":{"rank_math_lock_modified_date":false,"ep_exclude_from_search":false},"product_cat":[2851],"product_tag":[],"class_list":{"0":"post-334473","1":"product","2":"type-product","3":"status-publish","4":"has-post-thumbnail","6":"product_cat-joint-commission","8":"first","9":"instock","10":"sold-individually","11":"shipping-taxable","12":"purchasable","13":"product-type-simple"},"_links":{"self":[{"href":"https:\/\/pdfstandards.shop\/wp-json\/wp\/v2\/product\/334473","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/pdfstandards.shop\/wp-json\/wp\/v2\/product"}],"about":[{"href":"https:\/\/pdfstandards.shop\/wp-json\/wp\/v2\/types\/product"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/pdfstandards.shop\/wp-json\/wp\/v2\/media\/334482"}],"wp:attachment":[{"href":"https:\/\/pdfstandards.shop\/wp-json\/wp\/v2\/media?parent=334473"}],"wp:term":[{"taxonomy":"product_cat","embeddable":true,"href":"https:\/\/pdfstandards.shop\/wp-json\/wp\/v2\/product_cat?post=334473"},{"taxonomy":"product_tag","embeddable":true,"href":"https:\/\/pdfstandards.shop\/wp-json\/wp\/v2\/product_tag?post=334473"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}