Standard Operating Procedures (SOP)

Slides:



Advertisements
Similar presentations
Endothelial Progenitor Cell (EPC) Core Laboratory Instructions Version 5.0 March 29, 2008 For questions regarding collection, processing, storage, or shipping.
Advertisements

HES Data Management Ari Haukijärvi. Planning of HES Data Management Purpose of the data management The data will be available for analysis The available.
1 MTN-003 Study Specific Training Randomization Overview.
Unit 4: Specimen and Data Collection # Warm Up Questions: Instructions  Take five minutes now to try the Unit 4 warm up questions in your manual.
Blood Administration RPI Education Roll out Problem-there is a need for the blood administration process and associated documentation to be 100% accurate.
Biomarker Study Protocol WP 09, VHIR-Barcelona EudraCT-No.: Biomarker Study, Protocol Training, v1.0, June slides.
The Veterans Affairs Central Biorepository and MVP Highlights Mary T
IMMUNOLOGY LABORATORY PBMC ISOLATION SOP by Kizza D Martin Ssemambo
Customized Laboratory Support Roxann Neumann, RN, BSN, CCRP ACCRU Biospecimen Resource Manager.
Research Study Regulatory Binder Ronald Cowan, MD, PhD J. Gavin Lillevig, BS Summer Professional Didactics Data Management Psychiatric Neuroimaging Program.
EDRN’s Validation Study Information Management System Developed for EDRN by the DMCC Cancer Biomarkers Group Division of Cancer Prevention Jet Propulsion.
Human Specimen Repositories: Requirements of 45 CFR part 46 PRIM&R May 5, 2004 Julie Kaneshiro DHHS Office for Human Research Protections Phone:
1 MTN-003 Training Specimen Labeling and Preparation for Entry into LDMS.
Collection, Storage and Transport of Blood for HIV Testing
Use of Dried Blood Spots (DBS) Specimens for Measuring HIV-1 Viral Load in Argentina M. Lorena Vázquez Inés Zapiola Ana Gun Silvia Gómez Alejandro Krolewiecki.
Packaging and Shipping Frozen Specimens using Dry Ice
23/05/2015 THL Logistics System Marko Grönholm Diabetes Prevention Unit.
IRB 101: Introduction to Human Subject Research
Institutional Review Board (IRB) Process Tim Noe Coordinating Center.
Data Issues: Quality and Analysis By Ziyad Mahfoud, Ph.D. Associate Professor of Biostatistics Department of Public Health Ziyad Mahfoud, Ph.D.1.
Stroke Hyperglycemia Insulin Network Effort (SHINE) Trial I-SPOT Nina Gentile, MD Hannah Reimer.
Coordinator University Clinical Research Pharmacy Investigational Drug Service (IDS) Marjorie Shaw Phillips, MS, RPh, FASHP Clinical Research Pharmacist.
WP5 : omics Coordinators : Pr Marion Leboyer (France) Pr Dan Rujescu (Germany)
Labeling procedures for the 2005 PNG National Nutrition Survey.
Medicel Biobank Thomas M Attard MD FAAP FACG Consultant Pediatrician Kansas City Childrens Mercy Hospital, MO, Mater Dei Hospital, B’Kara, Malta Associate.
Synta Pharmaceuticals
6/1/09.
Newborn Screening Translational Research Network Coordinating Center Duane Alexander, M.D. Director, Eunice Kennedy Shriver National Institute of Child.
RESCUE: ACRIN 4701 Protocol Development & Regulatory Compliance (PDRC) Josephine Schloesser, ACRIN Monitor Chris Steward, ACRIN QC Auditor.
This teaching material has been made freely available by the KEMRI-Wellcome Trust (Kilifi, Kenya). You can freely download, adapt, and distribute this.
Labeling for the 2005 PNG National Nutrition Survey.
Tips for Researchers on Completing the Data Analysis Section of the IRB Application Don Allensworth-Davies, MSc Statistical Manager, Data Coordinating.
Stanley Estime, MSCI, CIP Senior QA/QI Specialist Lisa Gabel, CIP QA/QI Specialist IRB Determinations: What type of Review will your study receive?
Joyce Mull, MPM Director, Regulatory Affairs National Surgical Adjuvant Breast and Bowel Project Consent Form and IRB Challenges that Arise with Specimen.
Informed Consent Process: Key Considerations. Introduction  Informed consent is a requirement of ethical clinical research  Section 4.8 of the International.
Paula Peyrani, MD Division of Infectious Diseases University of Louisville The IRB Process What do I need to know? The IRB Process.
Expedited Review – Retrospective studies: A New Path Stephanie Gentilin, MA, CCRAKatherine Bright Director SCTR SUCCESS Center, eIRB Team MemberIRB, Grants.
Urine Collection.
Privacy vs. Confidentiality.  IRB review of privacy and confidentiality protections is required under the Common Rule and the FDA regulations, as well.
Tele-Medicine Risk Adjustment. Agenda What is Medicare Risk adjustment? Conclusion Summery of project specification Why Tele-Medicine? Team Workflow Design.
Module 8: Blood Collection and Handling Dried Blood Spot
Laboratory analysis Georg Alfthan. Selection of blood measurements Core measurements: CVD risk factors Additional measurements: CVD, Diabetes, Dietary.
V Overview of PBMC, Serum, Plasma and CSF Samples Holly Lash, Research Biochemist Jennifer Talaty, Medical Program Coordinator.
Data Management Seminar, 9-12th July 2007, Hamburg Within-School Sampling – A General Introduction.
The UWCCC/WON Molecular Tumor Board (MTB) & Registration Protocol Mark E. Burkard MD PhD WON fall meeting October 24, 2015.
Study Forms Subject Enrollment Log Demographic/Clinical Form Cold-chain Maintenance Form Result of Rapid Diagnostic Test for Influenza Form.
Sponsor Visits and Monitoring
Sample Collection Training Guide. Sample Collection Overview It is the responsibility of the transfusing facility to collect and properly label blood.
Michael J. Bell, MD Stephen R. Wisniewski, PhD University Of Pittsburgh National Institute Of Health National Institute Of Neurological Disorders And Stroke.
Introduction and Training 1 By: Snehil Gupta CBMI, WUSTL.
Slide 1 Standard Operating Procedures. Slide 2 Goal To review the standard operating procedures Creating the informed consent document Obtaining informed.
Managing Patient Contact Studies at a Central Registry
Study population Women years old in 2005
The LAASER program Raphael Hamers, MD
Houston Methodist Diagnostic Laboratories
ENTRY ID LABEL ENTRY ID LABEL ENTRY ID LABEL ENTRY ID LABEL
EDRN’s Validation Study Information Management System
The idea Policy Process Procedure.
Lana Gevorkyan Corporate Director Human Research Protection Program
FaceBase Biorepository: Overview
Primary Health Care (PHC) Laboratory tool kit
MTN 037 Laboratory Training
REDOXS Training: Introduction & Site Investigator
THE OPTIONAL GENETIC STUDY
Exam Room Health Center Health Center Front Desk Waiting Room
Human Subject Research
TRACE INITIATIVE: Specimen Collection, Handling, & Transport
TRACE INITIATIVE: Data Collection Tools and Forms
Overview of the POC EID Training Toolkit
Presentation transcript:

Standard Operating Procedures (SOP) Julie Mook-Kanamori Clinical Research Coordinator

Overview Categories of SOPs Example SOP Blood Sample Kits Label coding Case – Control Linking

SOPs Patient Visit SOP Workflow Step-By-Step SOP Patient Enrolment SOP Control Enrolment SOP Informed Consent Form

SOPs Data Collection SOP Demographics and Clinical Questionnaire SOP Ancestry Questionnaire SOP Using SurveyGizmo SOP Data Entry SOP Data Storage SOP Quality Control

SOPs Blood Samples SOP Creating Labels SOP Venepuncture SOP Sample Processing SOP Sample Shipment on Dry Ice

Example SOP Purpose Policy Responsibility Procedures Post-processing Contact for questions or injury

Blood Sample Kit 2x EDTA tube 4.0ml, pre-labeled 2x Cryovials 5.0ml, pre-labeled 6x SubjectID stickers Blood Specimen Collection form Contact Information form

Label Coding IRB-2011-0019 04-SubID 4001 Each country starts with 100 kits, for example 3001 to 3100 for Lebanon No linking codes between cases and controls  linking log sheet Site Site code Available numbers Jordan 1 1001 – 1999 KSA 2 2001 – 2999 Lebanon 3 3001 – 3999 Qatar 4 4001 – 4999 UAE 5 5001 – 5999

Case – Control Linking Linking log sheet Subject ID Age Sex Ancestry

Questions Are there any questions?