« A Driver becomes Monitor » Philippe Van der Hofstadt B & C International, Belgium Conférence CEMO 14 Mars 2001.

Slides:



Advertisements
Similar presentations
MONITORING OF SUBGRANTEES
Advertisements

Maintenance, Management and Monitoring of Investigational Supply
Tips to a Successful Monitoring Visit
Tour Guides Expertise. Chapter 4 Service Regulations for Tour Guides Part A Tour Guide Local Guide National guide Tour Leader.
AIMS Science Pre-Test Training Session 1 School Year Presented by Arizona Department of Education and Pearson.
On-Site Services Spectrum BioScience … –Saves you time by Doing routine tasks non-core related –Saves you money… Connects you to researched sources of.
Neoteric Technology Ltd – All Rights Reserved - © 2006
Understanding & Using the USPS DSMS System The Benefits, Requirements Added Value of the Drop Ship Management System.
PROVIDE ARRIVAL AND DEPARTURE ASSISTANCE
Developed by Klinikos; Roy Fraser (2012) Investigator Study File
Managing Sponsorship Research Services University of Oxford.
Tipologie di Audit e loro caratteristiche Riunione sottogruppo GCP-GIQAR 21 Marzo 2006 Francesca Bucchi.
9 C H A P T E R Transaction Processing and Enterprise Resource Planning Systems.
PMI Inventory Tracker™
D. Keane June Internal Quality Audits (4.14) -ISO Requirements for Internal Audits -The Audit Process -Templates for Meeting Requirements.
October Module 7: Recordkeeping Overview: In this section, you will learn about records required for each job. Records must be retained and made.
Specialists in Data Capture, Barcode, RFID, Voice & Vision BEC (Systems Integration) LTD Case Study – Alstons Electronic Proof of Delivery Andrew Briggs.
Clinical Pharmacy’s Role in Research Trials Sheree Miller Pharm.D. Investigational Drug Service University of Washington Medical Center.
Bill Brisiel – Shipping/Receiving Manager Music by Dr. Simon Taylor PHD.
Courier Service Membership Program Nancy Nathanson, Systems Manager.
Update on the Enterprise Initiative: e-IRB and More Riyad Naser, MS, MBA Director of Research Information Systems Karen Blackwell, MS, CIP Director, Human.
1 © CINECA 2012 CINECA web based platform In supporting of Ethics Committee activities July 2013.
February 2007 Commercial Vehicle Drivers Hours of Service Module 24: Daily Log Audits.
Elements of Clinical Trial Quality Assurance Regulatory Coordinator –SCTR SUCCESS Center QA Monitor – NIDA Clinical Trials Network Stephanie Gentilin,
Rutgers University Future state monthly close calendar
MODULE I Close-Out Visit/Monitoring Reports Jane Fendl April 24, Versions: Final 24-Apr-2010.
Joint Research & Enterprise Office Training The team, the procedures, the monitor and the Sponsor Lucy H H Parker Clinical Research Governance Manager.
MODULE B: Case Report Forms Jane Fendl & Denise Thwing April 7, Version: Final 07-Apr-2010.
Monitoring IRB Monitoring of Clinical Trials. Types of Monitoring Internally Internally Externally Externally.
4C’s Clinic Redesign Operational Snapshot July 28, 2005.
CLINICAL TRIALS – PHASE III. What are phase III trials  Confirmatory phase (Therapeutic confirmatory trial)  Trials are done to obtain sufficient evidence.
Chapter 8 Transaction Processing, Electronic Commerce, and Enterprise Resource Planning Systems.
TST BOCES SCOOLS (South Central Organization of (School) Library Systems) INTERLIBRARY LOAN PROCESS…..An Overview Created by Michele Barr, TST ILL Login.
Investigator’s Meeting
Continuation Training Record Keeping Meet the challenges of Ilka Wolf, Marketing & Sales.
Home delivery – Clotting Factors Edinburgh – 4 th January 2007 Dominic Moreland – Managing Director, Careology Mandy Wakefield – Director of Nursing, Careology.
Pharma Logistics. About Q-Pharma Logistics Pharmaceutical freight is a service that comes with many challenges; however, in collaboration with renowned.
JWST PRDS Project Mangement Case Study Jesse Doggett Project Engineer, ITEB/OED.
Sydney (02) Melbourne (03) Brisbane (07) Carlo Biaro Capital Insight Conference 2013 – Tools and.
RIHES-II: H ANDLING A UDITS AND I NSPECTIONS E FFECTIVE D ATE 25 D ECEMBER 2006 V ERSION : 3.0 บุญเหลือ พรึงลำภู 15 มกราคม 2557.
CLINICAL RESEARCH STUDIES Business & Finance (B &F) Prospective Patricia W. Davis Director of Research Office of Business & Finance
SFA At-Risk Afterschool Meal Program Training Recordkeeping and Monitoring.
IP Accountability in Outpatient Clinical Trials
RIHES JJ: Required Training Version 7.0 Effective Date 27 JAN 2011 Boonlure Pruenglampoo 15 Jan 2014 วันพุธที่ 15 มกราคม พ. ศ 2557 RIHES-JJ Version 7.0.
Sponsor Visits and Monitoring
Assessing Logistics System Supply Chain Management 1.
PTC Project Update 13 th June Advantages of Services of PTC – By Chin Szi Chu’en 2.PC GTN Process Flow– By May (PC Mgr) 4. PTC Update – By Zaid.
Pharmacy Training Protocol Version: 31 August 2015.
Logistics. Transport - Personal Troops will be travelling to & from AJ2016 via Coach Dedicated central pick up locations per troop*Dedicated central pick.
Site Set-up and Conduct Caroline O’Leary and Carrie Bayliss.
IP Accountability in Outpatient Clinical Trials Jessica Rinaldi, CCRP Farber Institute for Neurosciences.
Colleges & Universities Delivery Partners Program
Design of Case Report Forms
Outbound Process Using Wave, Pick-HU, Packing, Staging, and Loading
PRCSG Training Webinar: Budget for Industry Sponsored Studies
Software Application Overview
ROUTE MANAGER TRAINING
Investigator of Record – Definition
Alliance Data Research and SIS Teams
Jessica Dare, Principal Consultant
CBI - Clinical Trials Budgeting and Forecasting
Quality Control SOP 3.12 Release Date: 08/10/2015.
Investigator of Record – Definition
Investigator of Record – Definition
The Interlink Express one hour delivery window
MiSLE Investigational Product Training
Shipping, Receipt and Infusion February 2019 Update
Qualtrics for data collection
Doing Business with the Business Office
Presentation transcript:

« A Driver becomes Monitor » Philippe Van der Hofstadt B & C International, Belgium Conférence CEMO 14 Mars 2001

Working method 1. Initiation 2. Planning 3. Pick-up4. Delivery 5. Completion

1. Initiation Collect site info for pick-up & delivery Confirm pick-up & delivery frequency Prepare study-specific transport protocol Sign transport protocol Prime the study database

Study-specific transport protocol Communication procedure Pick-up & delivery frequency Required transport documents Required data check on-site vs request form # samples/visit Patient demographics Collection date & time … Data cleaning procedure

2. Planning Call sites to confirm sample availability Plan routes in routing software Book travel arrangements (hotel, shuttle, ferry,…) Confirm pick-up date & time to sites Confirm to Lab/Sponsor final pick-up schedule

3. Pick-up Prepare materials Arrival on-site Scan bar-codes Data check Print pick-up note Upload data to office Download route from office

4. Delivery Arrival on-site Deliver frozen samples Print delivery note Departure Upload data to office

5. Completion Pick-up confirmation to Lab/Sponsor next morning Delivery confirmation to Lab/Sponsor next morning

Advantages Investigator No need to call Courier/Lab Scheduled pick-up date and time Dry ice delivered to site personnel Samples packed by driver No worry about sample shipment dates

Advantages Central Labs Pick-up schedule known in advance Daily pick-up confirmation Inconsistencies identified/corrected on- site Feedback from site non-compliance Sample tracking through lab barcode Increased interaction with sites e.g. expired kits «Training » from site personnel

Advantages Sponsor Improved service to Investigators Increased protocol compliance Additional site monitoring Feedback from site non-compliance

Future developments Consolidated clinical trial transport On-site training Bidirectional e-link Lab-Courier Automated data cleaning on-site On-site lab data entry