Immunohistochemistry Validation: Past, Present and Future Philip Ferguson M.D. Validation procedures are part of the regulatory process in a laboratory setting. Understanding the basic principles and reasons for validation is important for laboratory compliance of regulations and eventually for patient diagnosis and treatments of diseases. A discussion of current trends and changes with the latest CAP checklist will be reviewed and future direction of where IHC validation may end up will be discussed. 학습 목표 Understanding of the basic principles and reasons for the validation process. Describe historical perspective of past IHC validation requirements. Discuss current trends and changes in validation requirements (CAP latest checklist). Examine the future direction of where the IHC validation process may end up. 발표자 소개 Philip Ferguson , M.D. Dr. Philip Ferguson is in a private practice located in Arkansas. He has a diverse training background that includes an undergraduate degree in mechanical engineering, post-graduate training in internal medicine, and board certifications in anatomic pathology, clinical pathology, and hematopathology. His professional interests center around educational resource development for pathologists and trainees, and use of immunohisochemistry and molecular diagnostics in surgical pathology. Dr. Ferguson launched one of the first widespread internet educational tools for pathology residents to prepare for their board examination, PathMD (www.PathMD.com), which is now the Leica tool PathLead. Dr. Ferguson also serves as a state commissioner for the College of American Pathologists' Accreditation and Laboratory Improvement Program and is also member of the Global Advisory Board for Leica Biosystems. Dr. Ferguson has published several publication of late including ‘The Effect of Decalcification Solutions on Kappa and Lambda In-Situ Hybridization,’ as well as ‘Effects of Decalcification on Immunohistochemistry Comparing: Immunocal®, Formical2000®, and EDTA Stat®.’ 라이카 바이오시스템즈 Knowledge Pathway 콘텐츠는 에서 이용할 수 있는 라이카 바이오시스템즈 웹사이트 이용 약관의 적용을 받습니다. 법적고지. 라이카 바이오시스템즈 웨비나, 교육 프레젠테이션 및 관련 자료는 특별 주제 관련 일반 정보를 제공하지만 의료, 규정 또는 법률 상담으로 제공되지 않으며 해석되어서는 안 됩니다. 관점과 의견은 발표자/저자의 개인 관점과 의견이며 라이카 바이오시스템즈, 그 직원 또는 대행사의 관점이나 의견을 나타내거나 반영하지 않습니다. 제3자 자원 또는 콘텐츠에 대한 액세스를 제공하는 콘텐츠에 포함된 모든 링크는 오직 편의를 위해 제공됩니다. 모든 제품 사용에 다양한 제품 및 장치의 제품 정보 가이드, 부속 문서 및 작동 설명서를 참조해야 합니다. Copyright © 2024 Leica Biosystems division of Leica Microsystems, Inc. and its Leica Biosystems affiliates. All rights reserved. LEICA and the Leica Logo are registered trademarks of Leica Microsystems IR GmbH. Knowledge Pathway의 이 교육용 웨비나, 학습 자료 또는 자습서를 보고 인증 기관에 교육 크레딧을 신청하려면 다음 양식을 다운로드하십시오. 획득한 교육 크레딧을 개인 성적표에 직접 기입할 수 있습니다. (단, 대한민국은 적용 대상 아님) 자가보고식 교육학점을 신청 하세요 최신 Knowledge Pathway를 이메일로 직접 받아볼 수 있습니다. 지금 구독하세요! 더 많은 훌륭한 집필진을 기다리고 있습니다. 원고를 보내주시면 담당자가 연락드리겠습니다. Send your writing! SHARE Facebook Twitter LinkedIn Email
Validation procedures are part of the regulatory process in a laboratory setting. Understanding the basic principles and reasons for validation is important for laboratory compliance of regulations and eventually for patient diagnosis and treatments of diseases. A discussion of current trends and changes with the latest CAP checklist will be reviewed and future direction of where IHC validation may end up will be discussed.
