Lessons Learned from the QC Process in Outsourcing Model Faye Yeh, Takeda Development Center Americas, Inc., Deerfield, IL



Similar documents
A Comparison of Two Commonly Used CRO Resourcing Models for SAS/ Statistical Programmers R. Mouly Satyavarapu, PharmaNet/ i3, Ann Arbor, MI

PharmaSUG Paper IB05

Quality Assurance: Best Practices in Clinical SAS Programming. Parag Shiralkar

How To Write A Clinical Trial In Sas

Synergizing global best practices in the CRO industry

Implementation of SDTM in a pharma company with complete outsourcing strategy. Annamaria Muraro Helsinn Healthcare Lugano, Switzerland

QUALITY CONTROL AND QUALITY ASSURANCE IN CLINICAL RESEARCH

Using SAS Data Integration Studio to Convert Clinical Trials Data to the CDISC SDTM Standard Barry R. Cohen, Octagon Research Solutions, Wayne, PA

Essential Project Management Reports in Clinical Development Nalin Tikoo, BioMarin Pharmaceutical Inc., Novato, CA

Statistical Operations: The Other Half of Good Statistical Practice

Innovation Quality Flexibility

Graphing Made Easy for Project Management

SDTM, ADaM and define.xml with OpenCDISC Matt Becker, PharmaNet/i3, Cary, NC

Workshop on Quality Risk Management Making Trials Fit for Purpose

How to build ADaM from SDTM: A real case study

Needs, Providing Solutions

Software Validation in Clinical Trial Reporting: Experiences from the Biostatistical & Data Sciences Department

Working Model for Effective Functional Service Provider (FSP) Collaboration

Bridging Statistical Analysis Plan and ADaM Datasets and Metadata for Submission

Section 1 Project Management, Project Communication/Process Design, Mgmt, Documentation, Definition & Scope /CRO-Sponsor Partnership

Paper DM10 SAS & Clinical Data Repository Karthikeyan Chidambaram

August

Comparing JMP and SAS for Validating Clinical Trials Sandra D. Schlotzhauer, Chapel Hill, NC

ClinPlus. Clinical Trial Management System (CTMS) Technology Consulting Outsourcing. Expedite trial design and study set-up

Best Practice Approaches to Improving Clinical Supply Chain Management. Matthew Do Client Development Lead Almac Pharmaceutical Services

PharmaSUG 2016 Paper IB10

From Validating Clinical Trial Data Reporting with SAS. Full book available for purchase here.

USE CDISC SDTM AS A DATA MIDDLE-TIER TO STREAMLINE YOUR SAS INFRASTRUCTURE

Best Practice in SAS programs validation. A Case Study

Introduction. The Evolution of the Data Management Role: The Clinical Data Liaison

PROJECT MANAGEMENT PLAN <PROJECT NAME>

Clinical Data Management. Medical Writing. Bio-Statistics & Programming

PharmaSUG 2015 Paper SS10-SAS

Lessons on the Metadata Approach. Dave Iberson- Hurst 9 th April 2014 CDISC Euro Interchange 2014

Use of standards: can we really be analysis ready?

The ADaM Solutions to Non-endpoints Analyses

Rationale and vision for E2E data standards: the need for a MDR

ProjectTrackIt: Automate your project using SAS

Clinical Data Management Overview

Clinical Data Management BPaaS Approach HCL Technologies

A white paper presented by: Barry Cohen Director, Clinical Data Strategies Octagon Research Solutions, Inc. Wayne, PA

PHASE 6: DEVELOPMENT PHASE

How to Use SDTM Definition and ADaM Specifications Documents. to Facilitate SAS Programming

SAS Drug Development User Connections Conference 23-24Jan08

SAS CLINICAL TRAINING

POLICY AND PROCEDURES OFFICE OF STRATEGIC PROGRAMS. CDER Master Data Management. Table of Contents

Normalized EditChecks Automated Tracking (N.E.A.T.) A SAS solution to improve clinical data cleaning

SAS System and SAS Program Validation Techniques Sy Truong, Meta-Xceed, Inc., San Jose, CA

Practical application of SAS Clinical Data Integration Server for conversion to SDTM data

PHASE 8: IMPLEMENTATION PHASE

U.S. Contract Research Outsourcing Market: Trends, Challenges and Competition in the New Decade. N8B7-52 December 2010

QualityView - a program database and validation documentation tool

PharmaSUG Paper PO24. Create Excel TFLs Using the SAS Add-in Jeffrey Tsao, Amgen, Thousand Oaks, CA Tony Chang, Amgen, Thousand Oaks, CA

OPERATIONAL PROJECT MANAGEMENT (USING MS PROJECT)

A white paper. Data Management Strategies

PharmaSUG 2014 Paper CC23. Need to Review or Deliver Outputs on a Rolling Basis? Just Apply the Filter! Tom Santopoli, Accenture, Berwyn, PA

PHASE 6: DEVELOPMENT PHASE

SCOPE MANAGEMENT PLAN <PROJECT NAME>

Careers in Biostatistics and Clinical SAS Programming An Overview for the Uninitiated Justina M. Flavin, Independent Consultant, San Diego, CA

Contents. Project Management: August 2005 Page 2 Clinical Research Operational Standards for Professional Practice for Professional Practice

REDUCING THE RISKS INHERENT IN EMERGENCY MEDICAL CONTACT AND UNBLINDING

Health Care Job Information Sheet #20. Clinical Research

National IT Project Management Methodology

Understanding CDISC Basics

Sanofi-Aventis Experience Submitting SDTM & Janus Compliant Datasets* SDTM Validation Tools - Needs and Requirements

PharmaSUG Paper CD13

Managing and Integrating Clinical Trial Data: A Challenge for Pharma and their CRO Partners

Barnett International and CHI's Inaugural Clinical Trial Oversight Summit June 4-7, 2012 Omni Parker House Boston, MA

Supporting a Global SAS Programming Envronment? Real World Applications in an Outsourcing Model

through advances in risk-based

Full-Service EDC as an Alternative to Outsourcing

BT Contact Centre Efficiency Quick Start Service

Data Quality in Clinical Trials: a Sponsor's view

Copyright 2012, SAS Institute Inc. All rights reserved. VISUALIZATION OF STANDARD TLFS FOR CLINICAL TRIAL DATA ANALYSIS

AGILE RANDOMIZATION AND TRIAL SUPPLY MANAGEMENT SOLUTIONS: A RECIPE FOR SPEED, SIMPLICITY AND SERVICE

PharmaSUG2010 HW06. Insights into ADaM. Matthew Becker, PharmaNet, Cary, NC, United States

PepsiCo Rapid Change Management Methodology Based on Global Best Practices Implementations Following Kotter s Model

ABSTRACT INTRODUCTION WINDOWS SERVER VS WINDOWS WORKSTATION. Paper FC02

Department of Administration Portfolio Management System 1.3 June 30, 2010

SEVEN WAYS THAT BUSINESS PROCESS MANAGEMENT CAN IMPROVE YOUR ERP IMPLEMENTATION SPECIAL REPORT SERIES ERP IN 2014 AND BEYOND

StARScope: A Web-based SAS Prototype for Clinical Data Visualization

PharmaSUG Paper DG06

ADaM Implications from the CDER Data Standards Common Issues and SDTM Amendment 1 Documents Sandra Minjoe, Octagon Research Solutions, Wayne, PA

Building and Customizing a CDISC Compliance and Data Quality Application Wayne Zhong, Accretion Softworks, Chester Springs, PA

Programme Guide PGDCDM

Paper PO03. A Case of Online Data Processing and Statistical Analysis via SAS/IntrNet. Sijian Zhang University of Alabama at Birmingham

KCR Data Management: Designed for Full Data Transparency

Development, Acquisition, Implementation, and Maintenance of Application Systems

U.S. Food and Drug Administration

COMMUNICATIONS MANAGEMENT PLAN <PROJECT NAME>

Infoset builds software and services to advantage business operations and improve patient s life

The QA Governance Methodology

PHASE IIB III. inventivhealthclinical.com

Overview. The Concept Of Managing Phases By Quality and Schedule

The Project Management Life Cycle By Jason Westland (A book review by R. Max Wideman)

Meeting Priorities of Biotech & Small Pharma Companies

Importing Excel File using Microsoft Access in SAS Ajay Gupta, PPD Inc, Morrisville, NC

Transcription:

ABSTRACT PharmaSUG 2015 Paper TT11 Lessons Learned from the QC Process in Outsourcing Model Faye Yeh, Takeda Development Center Americas, Inc., Deerfield, IL As more and more companies in the pharmaceutical industry (sponsors) adopt an outsourcing model for clinical studies, improving the quality control (QC) process has become one of the main discussions between sponsors and their vendors, in most cases, the clinical research organizations (CROs). This presentation discusses the questions often asked by statistical programmers: How to improve the communication between sponsors and CROs? How to improve the clarity of data and TLF (tables, listings, and figures) specification documents? How to manage the QC processes at both sponsors and CROs sites? What are the efficient ways to verify CRO s deliveries? Having worked as a statistical programmer at both pharmaceutical companies and CROs for more than 20 years, the author will share some experiences and lessons learned on these four topics. The paper will present some suggestions on how to improve the quality control process in the outsourcing model. It does not intend to make any judgment on the quality of works produced or process currently used by sponsors or CROs. INTRODUCTION In today s pharmaceutical industry, more and more pharmaceutical, biotechnology, and medical device companies (sponsors) adopt outsourcing models in conducting clinical studies, which include statistical analyses and SAS programming. The scope of outsourcing statistical analyses may include statistical analysis plans, shells for TLF (tables, listings, and figures), datasets such as SDTM, derived datasets like ADaM, and TLF output. This paper will only discuss the quality control related to these processes. Figure 1 shows a typical process flow for producing statistical analysis results for clinical studies, regardless of underlying business model. In an outsourcing model, preparation of specification documents may be done by sponsors or/and CROs, depending on the contract. However, in most of cases, the majority of production work related to datasets or/and TLF are done by CROs. Before the delivery of output, CROs use the QC process that was agreed upon with the sponsor to assure the quality of works. Nevertheless, there is always some degree of verification performed by sponsors on all or selected output delivered by CROs. This is done not only to ensure the quality of output, but also to help sponsors verify their derivation logic/algorithms used in analyses. Prepare Specification Documents Produce Datasets and TLF QC / Verification Findings or Comments No Ready for Finalization Yes Make Changes Figure 1 In outsourcing models, some of the main responsibilities of programmers at sponsor s site are to oversee and manage the timeline of CRO s deliveries, to review specification documents, and to verify datasets and TLF generated by CROs to ensure the quality of the output. Their challenges are to implement the following practices: A clear and efficient communication path throughout the project between sponsor and CRO Very well documented Specifications (such as statistical analysis plan, data specification, TLF Shells) A good QC process implemented at both sponsor and CROs site that would minimize timeline and resource strain Building up a collaborative and trusting team work environment In the remainder of the paper, I will share some lessons learned in these areas. 1

STREAMLINE COMMUNICATION CHANNELS Lesson learned #1: Assign key contact persons at both CROs and sponsors When statistical analyses procedure is one of the components included in outsourcing model, it is common practice to assign a key contact person at both sponsor and CRO site for the project. Depending on the extensiveness of the work involved in the project, sometimes it might be necessary to appoint one contact for statisticians and one for programmers as well. Due to the business nature of CROs, programmers at CROs are often assigned to projects from different sponsors during the same time period. The sponsors need to understand that, when not managed properly, communicating directly to CRO s individual programmers could cause interruption of their work and ultimately delay delivery. Spontaneous communication (phone conversations or even e-mails) also makes it difficult for tracking the decisions/changes made at the project level and would lead to confusion and miscommunication. Designating the key contact person would help to streamline the communication between sponsors and CROs. Some sponsors have few, or only one, strategic CRO partners. For those outsourcing models, there are liaisons from each function at both sides and their responsibilities are to help set up and improve business processes at CROs site and to ensure overall quality of CROs deliveries. Different from the liaisons, the key contact for a specific project should be those who are responsible for leading statistical analyses and programming for the specific project and are also involved in day-to-day works related to the project. The key contacts would be responsible to setup routine joint project meetings to discuss timelines, milestones, and any major issues that arise during the project. Though communications between individuals at both sites are encouraged for detail questions/issues, the key contacts should always be copied or informed on such communications. Lesson learned #2: Have a version control document to track the changes and updates After verifying analyses results or reviewing delivered specification documents, it is a good practice that sponsor s key contact consolidates all the comments before sending them out to the CRO. The documents used for tracking the sponsor s comments could also be used by the CRO to summarize the responses and resolutions. Table 1 shows an example of a tabulated document for this purpose in MS Word format. For large or/and complicated projects with more than two scheduled deliveries, many people use Excel files for such documents because it provides the benefits of keeping all comments/resolutions in one file. Protocol Number Study Number 101 Milestone DRUGXXX 100% Blinded Delivery Date 01/31/2015 Table 1 Verification/QC Issue Log 1. General Comments: Deliverable Name Commented by Comments CRO s Response/Resolution ADSL Smith K 1. xxxxxxxx 2. xxxxxxxx 1. xxxxx 2. xxxxx Table 1.1 Smith K 1. xxxxx 2. xxxxx 1. xxxx 2. xxxx WELL DOCUMENTED SPECIFICATION Lesson learned #3: Improve the clarity of data and TLF specification documents For insourcing models, sometimes programmers would be able to generate derived datasets and TLFs by directly referring to the SDTM specification (SPEC) and statistical analysis plan (SAP). This is especially common for sponsors who have a very well documented SOP, or for small organizations where statisticians and programmers share a lot of responsibilities. It seems like everyone knows what he/she is doing. Or if not, the person who knows is 2

very likely sitting in the next cube. In outsourcing models with statisticians and programmers in different office locations and different companies, programmers from CROs may have little knowledge of the project background. Therefore sponsors should make every effort to improve information sharing. Specification like data SPEC, SAP, and TLF shells are crucial documents. Before production of datasets and TLF is started, statisticians and programmers at the sponsor s site should work closely with internal team members from other functions to make sure these specification documents have been thoroughly reviewed and finalized before they are submitted to the CRO. No matter who would be responsible for generating these documents, statisticians and programmers from both sides should carefully discuss and review these documents and resolve any major issues. Sometimes it would be even beneficial to annotate TLF shells. Below is an example: This practice would be beneficial for handling complicated TLFs and o help CRO programmers have a clear understanding on the relationship between data SPECs and TLF shells. Lesson learned #4: Sponsors to provide consistency on analysis standard Sponsor statisticians and programmers should be consistently compliant to their analysis standards. Whenever a deviation must be made, it should be documented and shared with CROs. Below lists a few commonly discussed analysis standards: 1. Data handling rules such as missing values, missing or incomplete dates collected, and definition of baseline or post dose measurements. 2. Titles and footnotes used across many TLFs, such as footnotes related to baseline, treatment emergent adverse events (TEAE), etc. 3. Statistical reporting standards such as rules for rounding, decimal points displaying for analysis results 4. Derivation standard used in ADaM SPEC It is not uncommon that the SAP or TLF shells need to be modified or new variables or TLFs added. These specification documents should be updated and reviewed by both sites periodically and in a timely manner. The changes and updates should also be documented for a better tracking. BUILDING A COLLABORATIVE AND TRUSTING RELATIONSHIP Lesson learned #5: Share and understand partner s quality control process and standards. One of the main objectives for outsourcing model could be cost reduction. However, poor QC process management causes multiple changes/updates of datasets and outputs, and leads to timeline delays and increasing budgets. CROs and sponsors should discuss and understand their partner s quality control processes and standards. It is important that programmers at CROs are trained to understand and follow sponsor s quality control standards. For sponsors and CROs that have established a long-term partnership, this should be done on an ongoing basis and liaisons at both sites are responsible to monitor this process. If the contract is signed on a project basis, CROs should make sure any employees assigned to the projects are trained before the start of the project. Sponsors want to ensure there is a well documented QC process at CROs before actual production work starts. 3

Quality control relies on risk-based management. Errors or mistakes always live within our lives and works. Understanding the CRO s QC process and providing better training to the CRO s team members would help to boost the sponsor s confidence level on the products received from CROs. Therefore, the amount of verification/review works would be reduced at sponsor s site. Lesson learned #6: Delivering and finalizing unique sets of important output first When planning milestone delivery from CROs, sponsors may request CROs deliver the unique sets of important TLFs first. For example, in a project in which analyses are done for different subject populations, it would be more efficient to deliver all output only after major verification/review findings of output are resolved from the first selected population. This strategy could also be applied to a situation when there is a large quantity of TLFs that shared similar formats, such as summary tables for TEAE, related TEAE, Serious TEAE, etc. Lesson learned #7: CROs to provide sponsor the transparency of their analysis processes We understand that using well-developed and validated macros for production work can greatly improve the efficiency, quality, and consistency of the statistical analysis outputs and data sets. Programmers from CROs should help sponsors better understand global macro systems implemented for the project. If the current project is very similar to a previous one that CRO had worked on, programmers from both sites should discuss the possibility of carrying works and experience from previous project to the new project. CROs are encouraged to discuss and share the QC plan with sponsors during the planning stage. The QC plan usually provides detail information such as QC methods (independent programming, code review, visual checks, and cross checks) and QC coverage (full or partial QC). A QC check list from CROs could also be used to helps sponsors gain clear pictures of QC work conducted at the CRO site. In dealing with large and complicated data, programmers from both sites may need to exchange SAS codes and log files to resolve QC issues. CONCLUSION In outsourcing models, building a cooperative and trusting team work environment is always a critical factor to the success of project. Both sponsors and CROs should strive hard to cooperate with each other by establishing an efficient and flexible communication channel, understanding and implementing standards and processes at both sites, and providing each other a clear and organized documentation system. REFERENCES Satyavarapu, R.Mouly (2012): A Comparison of Two Commonly Used CRO Resourcing Models for SAS/Statistical Programmers. Proceeding of PharmaSUG 2012 Conference Benze, Keith C (2005): Risk-Based Approach to SAS Program Validation. Proceeding of PharmaSUG 2005 Conference Tyson Gary and Dietlin (June 2004): Working with CROs. Pharmaceutical Executive ACKNOWLEDGMENTS I would like to thank Wei Qian, Fima Gershteyn, Lorraine Spencer for reviewing this paper and for providing useful feedback. CONTACT INFORMATION Your comments and questions are valued and encouraged. Contact the author at: Name: Faye Yeh Enterprise: Takeda Development Centers Americas, Inc Address: 1 Takeda Pkwy City, State ZIP: Deerfield, IL 60015 Work Phone: 224-554-2733 E-mail: faye.yeh@takeda.com Web: www.takeda.com 4

SAS and all other SAS Institute Inc. product or service names are registered trademarks or trademarks of SAS Institute Inc. in the USA and other countries. indicates USA registration. Other brand and product names are trademarks of their respective companies. 5