Final Business Plan Q10: Pharmaceutical Quality Systems dated 14 October 2005 Endorsed by the ICH SC on 10 November 2005



Similar documents
ICH Public Meeting. Joseph C. Famulare. October 2, Acting Deputy Director Office of Compliance CDER / FDA Office of Compliance

Introduction to Q10 Pharmaceutical Quality System

ICH Q10 Pharmaceutical Quality System (PQS)

Guidance for Industry. Q10 Pharmaceutical Quality System

PHARMACEUTICAL QUALITY SYSTEM Q10

INTERNATIONAL CONFERENCE ON HARMONISATION OF TECHNICAL REQUIREMENTS FOR REGISTRATION OF PHARMACEUTICALS FOR HUMAN USE Q4B ANNEX 12

Industry Implications of Pharmaceutical Quality ICH Guidelines

EXPERT REVIEW PANEL PROCEDURE: ADDITIONAL SUPPORT TO PROCUREMENT AGENCIES UNDER EXCEPTIONAL CIRCUMSTANCES

Guidance for Industry

ASSESSMENT OF QUALITY RISK MANAGEMENT IMPLEMENTATION

EVALUATION AND RECOMMENDATION OF PHARMACOPOEIAL TEXTS FOR USE IN THE ICH REGIONS ON TABLET FRIABILITY GENERAL CHAPTER Q4B ANNEX 9(R1)

Aligning Quality Management Processes to Compliance Goals

Managing the Cost of Compliance in Pharmaceutical Operations 1

EU Change Control Process for Change Requests in the Entire Area of Electronic Submissions for Human Medicinal Products Version 2.

Regulation and Risk Management of Combination Products

Comparative analysis between the possible regulatory approaches to GMP compliance TITOLO PRESENTAZIONE

How companies leverage quality and quality certifications to achieve competitive advantage

Common Student Information System for Schools and School Boards. Project Summary

The Clinical Trials Directive in the EU: Present and Future Elisabethann Wright, Partner Maurits Lugard, Partner. May 2010

Optimizing Quality Control / Quality Assurance Agents of a Global Sourcing / Procurement Strategy

Guideline for Industry

Clinical trials regulation

Pharmaceutical Distribution Security Alliance (PDSA)

Drug Development Models in China and the Impact on Multinational Pharmaceutical Companies

PROJECT INFORMATION DOCUMENT (PID) ADDITIONAL FINANCING Report No.: PIDA Project Name Parent Project Name. Region Country

Taking a Leap Toward Global Supply Chain Efficiency

COMPLIANCE FRAMEWORK AND REPORTING GUIDELINES

Effective Model Risk Management for Financial Institutions: The Six Critical Components

Clinical Research in Mauritius

ICH Q9 Quality Risk Management - an industry view. Peter H. Gough, Eli Lilly and Company

Overview. Health Science Authority. Implementation of ICH guideline in Singapore. Singapore s experience

INTERNATIONAL CONFERENCE ON HARMONISATION OF TECHNICAL REQUIREMENTS FOR REGISTRATION OF PHARMACEUTICALS FOR HUMAN USE. Current Step 4 version

ICH guideline Q10 on pharmaceutical quality system

Quality Management Subcontractor QM Guide-Section Two

EU DIRECTIVE ON GOOD CLINICAL PRACTICE IN CLINICAL TRIALS DH & MHRA BRIEFING NOTE

Working Party on Control of Medicines and Inspections. Final Version of Annex 16 to the EU Guide to Good Manufacturing Practice

How CMOs are Turning Their Training Programs into Market Differentiators

INTRODUCTION. This book offers a systematic, ten-step approach, from the decision to validate to

Quality Risk Management The Pharmaceutical Experience Ann O Mahony Quality Assurance Specialist Pfizer Biotech Grange Castle

Identification of Medicinal Products (IDMP) What is necessary in order to be compliant in 2016 and beyond?

Review of the Implementation of IOSCO's Principles for Financial Benchmarks

A Stability Program for the Distribution of Drug Products

Patient Centric Monitoring Methodology

Managing Paper at Its Roots: Extending Beyond Document Management to Enterprise Content Compliance

Improved Utilization of Self-Inspection Programs within the GMP Environment A Quality Risk Management Approach

Medical Product Development Certificate Program

GUIDELINE NO. 22 REGULATORY AUDITS OF ENERGY BUSINESSES

Private Certification to Inform Regulatory Risk-Based Oversight: Discussion Document

Guidance for Industry and FDA Staff FDA Acceptance of Foreign Clinical Studies Not Conducted Under an IND Frequently Asked Questions

PROJECT MANAGEMENT FRAMEWORK

Recent Updates on European Requirements and what QPs are expected to do

New Energy Jobs Fund. Application Guidelines

ICH Q10 - Pharmaceutical Quality System

The purpose of this Supplier Quality Standard is to communicate the expectations and requirements of Baxter Healthcare Corporation to its suppliers.

Standardizing Best Industry Practices

Conducting a Gap Analysis on your Change Control System. Presented By Miguel Montalvo, President, Expert Validation Consulting, Inc.

Shared Assessments Program Case Study

Product Lifecycle Management for the Pharmaceutical Industry

Auditing as a Component of a Pharmaceutical Quality System

Michael Kickuth and Thomas Friedli

Welcome to the training on the TransCelerate approach to Risk-Based Monitoring. This course will take you through five modules of information to

Plumbing and Drainage Regulation 2012

Lifecycle CMC Management: ICH Q12 Progress to date

The European Clinical Trials Framework Update on the Draft Clinical Trials Regulation

Unedited version adopted by the 45th WHO Expert Committee on specifications for pharmaceutical preparations. World Health Organization 2010

Session 6: WHO Prequalification Programme. Key Process Steps WHO: Medicines UNFPA: Condoms and IUDs

Health Canada s GCP Compliance Program. GCP Information Sessions November 2010

Richard T. Clark Chief Executive Officer and President. Executing on Our Strategy

Emptoris Contract Management Solution for Healthcare Providers

Annex 10 Procedure for prequalification of pharmaceutical products

This interpretation of the revised Annex

Cost of Poor Quality:

Quality Risk Management

Specific Conditions for the Assessment of Management Systems and Product Certifications

Serious about safety. Seriously strategic about labeling. If you are serious about safety, you have to be seriously strategic about your labels.

Office of Inspector General Evaluation of the Consumer Financial Protection Bureau s Consumer Response Unit

Making Ontario a Preferred Location for Global Clinical Trials

Official Journal of the European Union. (Acts whose publication is obligatory)

Master Data Management For Life Sciences Manufacturers

Adventist HealthCare, Inc.

Data Quality Assessment. Approach

Section 6. Governance & Investment Roadmap. Executive Governance

ISPE Quality Metrics Project

End of consultation (deadline for comments) 14 October Adoption by Committee for advanced therapies 15 October 2010

Global regulatory affairs role in the biopharmaceutical industry

CSR / Sustainability Governance and Management Assessment By Coro Strandberg Principal, Strandberg Consulting

Transcription:

INTERNATIONAL CONFERENCE ON HARMONISATION OF TECHNICAL REQUIREMENTS FOR REGISTRATION OF PHARMACEUTICALS FOR HUMAN USE Final Business Plan Q10: Pharmaceutical Quality Systems dated 14 October 2005 Endorsed by the ICH SC on 10 November 2005 The issue and its costs: Currently, there are differences between industry and regulatory agencies in the different regions in the definition and interpretation of quality system terms, principles, application and expectations. Therefore, while the three regions are using various aspects of quality systems and concepts, a strong potential exists for further divergence. This divergence can occur in expectations and interpretations as the quality systems evolve, especially when implementing quality by design, continual improvement and quality risk management. This divergence is not in line with the need for an efficient and effective industry and regulatory processes. The absence of an internationally harmonized pharmaceutical quality systems guideline that manufacturers can use in assessing their process, products and systems can have the following impact on the patient, regulator and/or industry: Fragmented or fundamentally divergent approaches to quality systems are likely. Suboptimal deployment of limited resources to identify, enact or support effective elements of a quality system and continual improvement by both industry and regulatory agencies. Delays may occur in the availability of medicines to patients around the world. Delays in the implementation of innovation and continual improvement for existing products may occur due to different expectations in the three regions. Delays in the launch of new products. Different approaches between the three regions to compliance inspections. Impediments to moving within pharmaceutical manufacturing and associated regulatory processes towards implementing a culture of quality by design, right first time and continual improvement, as practiced within other industries. - 1 -

Planning: Because of the broadness and complexity of the guideline and as this guideline will be applicable over the life cycle of the product, it is important that EWG members have expertise in quality systems, compliance, pharmaceutical development, and manufacturing. In order to have the appropriate expertise and to keep the size of the EWG manageable, it is suggested that each ICH partner have the flexibility to nominate up to three experts to allow for a broad range of subject expertise to be adequately represented. The core group would be comprised of these nominees from each of the ICH parties and one representative from each observer (including EFTA, IGPA, WSMI, WHO, and Canada). It is anticipated that such a harmonised guideline (to step 2) could be developed within an 18 month period, assuming input of 18 man days per expert working group member for essential meetings over this period and 24 man days of input from an appointed Rapporteur. Additional input would be expected from observers. Progression to step 4 is anticipated to be less resource intensive. Timeline Adoption of topic by Approval of ICH Steering Committee to develop concept paper May, 2005 Approval of Concept Paper by Steering Committee November 2005 First EWG Chicago, USA November 5-10, 2005 Second EWG Yokohama, Japan June, 2006 Adoption of Step 2 Document Spring 2007 Risk Analysis The main risks associated with this project are the possibility of significant disagreement between the experts who might prevent or protract the development of a harmonised guideline. Several examples exist for multi-national harmonisation of documents that define quality systems. Therefore the risk of not achieving harmonization is low. In addition, it is expected that the guideline can be modelled after the FDA s recently issued draft guideline entitled Quality Systems Approach to Pharmaceutical Current Good Manufacturing Practice Regulations which serves as a bridge between existing GMP regulations and current understanding of quality systems. These risks should be mitigated by oversight of the process by the Steering Committee and review against the timelines proposed. - 2 -

Impact of the project: Potential Benefit There are areas where substantial cost benefits are envisaged as a result of the implementation of a quality systems guideline in parallel with it enabling the use of Q8, Q9 and potential future changes to regulations. Improved process performance. A reduction in the costs of internal failures (rejects, reworks, reprocessing and investigations) as the quality systems guideline drives improvement. A reduction in the costs of holding duplicate stock and operating multiple processes as improvements and changes are made more effectively across all regions. A reduction in the costs of preparing / reviewing certain regulatory submissions. Enhanced assurance of consistent availability of medicines to the patient. If only a small percentage of these costs could be avoided, then substantial saving of resources by industry and regulators will be realised and the benefits of this project will greatly exceed the costs. Achieving these savings is possible if industry can fully realize the benefits of ICH Q8 and Q9, and a harmonized ICH quality systems guideline. In a report entitled The Metamorphosis of Manufacturing, from Art to Science, published by IBM Business Consulting in May 2005, the authors indicated that their analysis showed that improving the performance of a process from 2.5 sigma (their current estimate of pharmaceutical manufacturing) to 4.5 sigma (their benchmark for good pharmaceutical manufacturing) yields a 1,000-fold greater decrease in defect rates when compared to improving the performance of the quality control system (i.e. inspection) from 5 to 5.5 sigma. Furthermore, they estimate that that a resulting decrease in internal failures could reduce the cost of goods by up to 3% and increase process performance significantly. For the top 30 pharmaceutical companies, IBM estimates the annual savings to be in excess of 8 billion. Estimated Implementation Costs The proposed quality systems guideline is focused on industry practice and will not itself define a new regulatory framework. The broad implementation of Q8, Q9 and a quality systems guideline may facilitate the initiation of changes in regional regulations; however, the nature of those changes is not within the scope of this guideline. Therefore, there will be no significant implementation costs for regulatory agencies aside from participation in the guideline - 3 -

development, education and publication processes. This cost will be mainly related to training of inspectors. The estimated cost to industry will vary across a very broad range based on a number of factors. The guideline is intended to be voluntary, and a firm may choose not to implement because they consider their current quality system a suitable alternative to that defined in the quality systems guideline, or because they choose to maintain the status quo. In this case, the cost to a firm could be zero. By maintaining the status quo, the firm chooses to operate within the current regulatory processes and may not benefit from any flexibility that may be associated with implementation of the guideline. If a firm decides to implement the quality systems guideline, the factors that will drive implementation cost include: Current state of the firm s quality system and extent of internal harmonization across sites Complexity of operations Number of operating sites The cost to implement a modern robust quality system should be viewed as an investment in efficient, high quality operations. Therefore, there will be a return on investment in cost savings resulting from efficiency improvements and lower internal reworks and rejects. In general, it can be assumed that the greater the opportunity to improve, the higher the cost savings resulting from the implementation. The costs of implementing a new or enhanced quality system are associated with 4 discrete steps: Assessment of existing corporate quality system versus ICH QS Guideline Design, redesign or enhancement of existing corporate quality system Assessment of required changes at operating sites to comply with updated corporate quality system Implementation of changes required at operating sites The range of man-days for these activities can be very roughly estimated. The estimates below are based on input from an independent quality system/gmp consulting firm. These estimates assume that a firm is compliant with existing GMPs and has at least a basic internal quality system. - 4 -

Assessment of existing corporate quality system versus ICH QS Guidance It is estimated that it would require between 10 and 20 man-days to complete an assessment and gap analysis of the current quality system versus a new ICH Guideline. The range is dependent on the size and complexity of the firm and the current state of the quality system. Design, redesign or enhancement of existing corporate quality system Enhancement of an existing quality system would be addressed through normal continuous improvement processes in accordance with a plan and timeline defined by the company. The cost for an enhancement is estimated to be nominal. If a partial redesign is needed, up to 160 man-days could be required to complete. The development of a totally new quality system could require up to 320 man-days for a larger, complex firm. Assessment of required changes at manufacturing sites to comply with updated corporate quality system For smaller firms with one or two manufacturing sites, the site assessment can be incorporated into the assessment of the corporate quality system and there will be minimal incremental costs. For larger firms, a separate site assessment may be warranted. It is estimated that it will require 20 40 man-days to conduct a comprehensive assessment against a newly designed or significantly redesigned corporate quality system. For enhancement to the corporate quality system, site assessments will be handled through the normal continuous improvement process at nominal cost. Implementation of changes required at manufacturing sites This number will vary greatly based on the current state of the corporate quality system, the extent of global implementation, the size of the firm, and the complexity of operations. An accurate estimate can only be established with a finalized quality system guideline and an assessment of the firm s current quality system versus the guideline. We can roughly estimate the time requirement to develop a comprehensive site quality system for firms with limited quality systems. For smaller and less complex sites, up to 200 man-days could be required to develop and implement all elements of a robust quality system at a site. For larger more complex sites, up to 800 man-days or more could be required. Firms will likely leverage the site development and implementation activities and each site will not have to incur this level of investment. - 5 -

The table below illustrates the estimated range of costs (measured in man-days that can be expected for each phase. Small Company Large Company Limited QS Robust QS Limited QS Robust QS Assess Corp 10 10 20 20 Design 160 nominal 320 nominal Assess Site 20 nominal 40 nominal Implement 200 nominal 800 + nominal Total 390 10+ 1180+ 20+ The actual monetary cost will depend on the region and whether internal resources or external consultants are used to complete the work. Under any situation, the implementation costs within a company are greatly exceeded by the potential benefits highlighted in the IBM report referenced above. Post-hoc evaluation: The results of implementing a harmonized quality system guideline can be measured in at least two areas; (1) improved process performance (sigma) resulting in lower rejects and (2) regulatory inspection findings that verify the robustness of a manufacturing site s quality system. October 14, 2005-6 -