Successfully reported this slideshow.
We use your LinkedIn profile and activity data to personalize ads and to show you more relevant ads. You can change your ad preferences anytime.

ePRO: Objective Patient Data Collection

406 views

Published on

This issue includes an article entitled PHT Auditing, featuring Rod Thorell, Director of Quality Management & Compliance at PHT Corporation; an interview entitled Why Auditing is Critical to Sponsors with Laura Araujo, a Senior Consultant of Quality Management at Halloran Consulting Group; and a brief Question/Answer segment with Rod that reviews the contemporary issues of auditing, and explains what sponsors commonly ask of PHT’s auditing processes and procedures.

Published in: Technology, Business
  • Be the first to comment

  • Be the first to like this

ePRO: Objective Patient Data Collection

  1. 1. PHT Insights — Third Quarter 2009 PHT Auditing Quality & ComplianceObjective Evidence that Data Collection ProcessesOperate Within Established Policies and Procedures This issue includes an article entitled PHT Auditing, written by Rod Thorell who Last quarter’s Insights Issue focused is Director of Quality Management & Compliance at PHT Corporation; an interview on data quality, security and privacy entitled Why Auditing is Critical to Sponsors with Laura Araujo who is a Senior matters, describing ‘How PHT Safeguards Consultant of Quality Management at Halloran Consulting Group; and a brief Electronic Patient Reported Outcome Question/Answer segment with Rod Thorell that reviews the contemporary (ePRO) Data Collected from Global issues of auditing, and explains what sponsors commonly ask of PHT’s Clinical Trials’. auditing processes and procedures. Similar to data security, PHT’s product suite is compliant with all archival requirements of Regulations and Guidance in the US, Japan and the Trust, but Verify–Russian Proverb European Union, as described in this Issue. PHT Auditing by Rod Thorell Director, Quality Management & Compliance Core to the founding principles of PHT, PHT Corporation September 2009 data quality, has been under the mandate of the company’s Chief Executive Recently, I was teaching one of my children how to responsible for the scientific integrity make a cake from scratch. As we put together all the of PHT’s product suite–Steve Raymond, ingredients, he grabbed a large container of what he Ph.D., Founder, Chief Scientific and thought was sugar. “Before you put it in,” I told him, “make sure you know what you have.” It was a simple Quality Officer. Our thanks to Steve for test to put a few of the little white granules on the tip of a finger then touch them his continuing contributions to PHT to the tongue. Instantly, it became obvious to him that it was salt, not sugar. Insights, his insistence that technology They look a lot alike, but have very, very different properties. I dare say that serve science, cake would not have been very palatable with a half cup of salt. Even though he and for his thought he was doing the right thing and everything appeared to be in order, a lasting gifts second person checking his process averted a certain disaster. and direction In any business, there are hundreds of processes that occur every day; some as to the clinical simple as baking a cake, some very complex involving people inside and outside and scientific the organization, crossing departmental functions and utilizing software or tools. industry The role of auditing is to at large. Contents provide objective evidence PHT Auditing p.1 that all those processes are Steve Raymond, Ph.D. running according to the PHT Founder, Chief Scientific and Quality Officer Interview with Rod Thorell p.3 policies and procedures PHT Corporation Interview with Laura Araujo p.4 put in place. Objective evidence gained about a
  2. 2. 2 PHT Insights – Third Quarter 2009 PHT Auditing and Quality Compliance participate in a full day of auditor training, led by a certified lead auditor. At the conclu- sion of the day, each new auditor is assigned an area or process to audit alongside an experienced auditor. When the audit report is completed, a second audit is planned with support from the Director of Quality and Compliance. After this second audit is com- pleted and reviewed, the training certificate is issued and they are considered to be an official internal auditor. External Audits Confirm ISO9001:2000 Certification The PHT internal audit program is reviewed during the annual surveillance audit from the ISO9001:2000 registrar. This third party inspection peers into our processes, including the processes we use to manage our internal audits. Every three process allows you to make informed decisions about quality years, we undergo a more rigorous re-certification audit that of the final output. By proactive examination, we can identify involves multiple auditors at our operation for several days. potential weaknesses and address them before they cause PHT has passed this re-certification audit of our quality systems nonconformity (also known as Preventive Action). Proactively and processes twice, maintaining continual ISO9001:2000 cer- strengthening processes are a key part of continual improvement tification since December, 2002. PHT’s continual certification of the PHT Quality Management System. is important, because we are required to pass the inspection PHT Internal Audits provide PHT of our quality system and demonstrate continual improvement managers with information on “The role of from year to year. We must demonstrate with concrete evidence the following three aspects of that we have a good system that is always getting even better. auditing is to their systems: provide objective PHT Audits Every Clinical Trial An audit is performed against • Adequacy: Do PHT’s systems, evidence that all every clinical trial PHT executes. This allows us to ensure as they are designed, have the those processes consistency in our practices, including project management, potential to succeed? software development and document handling. The final are running archive for each trial is audited to ensure our customers will • Implementation: Are PHT’s according to have all the necessary evidence to allow evaluation of the conduct systems being implemented as the policies and and data of the trial so that regulatory authorities can easily deem designed? procedures put the trial records to be trustworthy. • Effectiveness: Are PHT’s systems in place.” Corrective and Preventative Action Process While proactively achieving their intended results? monitoring processes strengthen PHT systems, from time to PHT Auditor Training & Certification PHT utilizes people time non-conformances occur that require corrective action. within the quality department as the primary auditing resource. PHT’s Corrective and Preventive Action process includes follow- Additionally, there is a team of trained internal auditors from up audits that are used to ensure the corrections remain in across the organization. The use of trained internal auditors place and continue to be effective after the completion of the from different backgrounds and disciplines ensures fresh corrective action plan. These corrective action plans and follow-up perspectives. Like the processes they are auditing, specific audits are also readily available for reference before conducting SOPs, training and experience are necessary to perform internal future audits within these process and business areas. audits. Volunteers that come from management and staff
  3. 3. 3PHT Vendor Audits In addition to internal Interview with Rod Thorellauditing, PHT audits key suppliers of prod- Director, PHT Quality Management & Complianceucts and services. This gives us evidencethat key suppliers are following applicable What is your role at PHT?regulations, are maintaining effective As the Director of Quality Management and Compliance, I have the responsibility,internal policies and procedures and have accountability, and authority to plan, direct, and administer PHT’s qualityadopted appropriate industry best practice system. On any given day, that can mean duties as diverse as ensuring we arefor delivery of their products and services. prepared for pandemic illness that could immobilize many of our staff, reviewingFeedback from our audits allows our suppli- regulatory compliance of StudyWorks™ software requirements or welcoming oneers to strengthen their own quality systems, of the many customer auditors that visit us each year.creating stronger partners in business. What are the contemporary issues of auditing?Sponsor Audits of PHT As a supplierourselves, PHT is audited many times each Truthfulness! Coast IRB went from being a growing organization with revenuesyear by current and prospective customers of $9.3m to shutting its doors in under a month, with the US Government Accountability Office (GAO) probe and FDA warning letter scaring off existingand partners. These audits and evalua- and potential clients. In a recent undercover operation by the GAO, it has beentions, which have ranged from one person alleged that Coast IRB approved a fictitious protocol for research in humans,on site for a day to eight people over three claiming that the device was FDA-approved. These falsehoods led to calls fordays, are an excellent source of feedback institutional review board (IRB) reform and a warning letter for Coast.to strengthen our Quality ManagementSystem. Observations from these audits aretreated the same way we would any internal “Auditing is like pulling a thread-even the best garments have a few looseaudit by being entered into a tracking system threads. A good auditor knows the difference between a random loose thread andto ensure there is proper closure by the one that will unravel the entire sweater.”responsible functional area. We encourage Rod Thorell, Director, PHT Quality Management & Complianceany of our customers to take the time to visitour facilities. These audits can be coordinatedthrough PHT’s local account executive. What do PHT customers commonly ask of our auditing processes and procedures?PHT strives to maintain a comprehensive People want to be sure that our audit program is structured and audits areaudit program. The internal audits include performed by trained personnel that have some independence from the areaa broad range of processes from our core they are auditing. Audits also need to have follow-up on the findings andsoftware development practices to Study should be analyzed for trends that can then be reported to senior management.Support Center operations, even Senior There should be a ‘closed-loop’ system to ensure that audit observations areManagement. These business processes resolved. All of these are part of PHT’s internal audit program.must conform to all of PHT’s policies,procedures and ISO9001:2000 standards. How are FDA submissions affected by clinical data auditing processesFurthermore, as a manufacturer and service and procedures?provider to global clinical trials, PHT has At its best, auditing is about ensuring that sound processes and proceduresa commitment to ensure our processes exist and they were properly followed during the execution of an eClinical trial.conform to regulatory requirements in over By proactively analyzing ourselves, the products and services we provide have65 countries where we are engaged in clinical consistently proven to meet or exceed expectations of the regulatory inspectorstrials. Auditing allows us to ensure we are who review them.compliant with an ever-changing globalregulatory landscape and deliver products Rod is Quality Management Systems professional with over twenty years ofand services that reliably meet customer experience in the Pharmaceutical industry. He joined the Quality departmentrequirements. at PHT in March 2007. Prior to joining PHT, Rod worked with several large organizations, leading teams in the assessment, development and validation of computerized systems for GxP applications.
  4. 4. 4Why Auditing is Critical to Sponsors By Laura Araujo storage of data over time. The Quality System must identify Sr. Consultant, Quality Management critical processes and define them up front. An Audit can Halloran Consulting Group help identify if there are issues related to process or require- August, 2009 ments, and enable the company to take corrective action as soon as possible. As an independent Auditor, Laura Have you ever worked with the FDA on recreating a study? Araujo interfaces with a wide range No, but I have hosted many FDA inspections where the focus of biopharmaceutical organizations, has been completely on the audit trails: walking through them, guiding executives through trial explaining them, and ultimately showing control of studiespreparations and FDA inspections. Following are excerpts taken over time. Many people are mistaken in believing that technologyfrom a recent interview with Laura. companies like PHT provide software or devices as theirHow do you explain the auditing deliverable. The software and devicesfunction to your clients? are merely tools to assist in gathering “One of the most impressive things from aThe best way to think about audit- the data for a trial. The real deliverable for sponsor perspective of PHT is the Archive,ing is an activity of assurance and PHT is actually the Archive—including which enables every sponsor to completely all specifications, data, deliverables,continuous improvement—assuringyou are following your processes, recreate a trial with data and context, without and change control over the courseassuring you are collecting the any time limit. The Archive doesn’t require any of the trial. PHT’s responsibilities docorrect deliverables, assuring you additional funding (such as server support). not end at successful distribution ofcan recreate a study—and then The PHT Archive is the best example of devices. It ends when the Archiveevaluating results and output to is complete. complete trial validation and recreation I’vecontinually improve over time. Laura joined Halloran Consulting Group ever seen in my 25 years of process auditing.”What is your fundamental recom- in 2008, and assists biopharmaceuticalmendation to biopharmaceutical Laura Araujo companies with their quality manage-companies preparing for a clinical Certified Auditor and Corporate Trainer ment system implementation, softwaretrial? development, validation and training.The most important thing a company Laura brings over 25 years experiencecan do in preparation for running a clinical trial is to have clear in quality assurance, technology management and softwareand well defined processes up front. If you do, even the most development with a focus on the biotechnology and pharma-complex study is simple to audit. If you don’t have your processes ceutical industries. Prior to Halloran Consulting, Laura was Vicewell defined, including deliverables and responsibilities, even the President of Quality at Perceptive Informatics, a subsidiary ofsimplest Audit will be difficult, and the study may be unable to PAREXEL International, where she managed quality assurancebe recreated. and computer systems validation as well as corporate quality systems including validation, supplier management, internalCan an audit ‘fix’ data quality? audit program, regulatory, patient confidentiality and training.No, you cannot “audit in” data quality. The key to data quality Prior Perceptive, Laura was the Vice President of Quality,is ensuring that you have sufficiently defined and addressed Information Technology, Customer Support and Hostingall issues up front related to collection, security, integrity, and Services at Clinsoft.PHT Corporation info@phtcorp.com InsightsQ32009500 Rutherford Avenue www.phtcorp.comBoston, MA 02129 USA Copyright © 2009 PHT CorporationToll-Free: 877-360-2901

×