Adoption of International Conference on Harmonisation of Technical Requirements for the Registration of Pharmaceuticals for Human Use (ICH) Guidance: Q10: Pharmaceutical Quality System
Date Adopted: 2016/02/15
Effective Date: 2016/02/15
Our file number: 16-101419-273
Health Canada is pleased to announce the adoption of the ICH guidance Q10: Pharmaceutical Quality System.
This guidance has been developed by the appropriate ICH Expert Working Group and has been subject to consultation by the regulatory parties, in accordance with the ICH Process. The ICH Steering Committee has endorsed the final draft and recommended its adoption by the regulatory bodies of the European Union, Japan and USA.
In adopting this ICH guidance, Health Canada endorses the principles and practices described therein. This document should be read in conjunction with this accompanying notice and with the relevant sections of other applicable Health Canada guidances.
It is recognized that the scope and subject matter of current Health Canada guidances may not be entirely consistent with those of the ICH guidances that are being introduced as part of our commitment to international harmonization and the ICH Process. In such circumstances, Health Canada adopted ICH guidances take precedence.
Health Canada is committed to eliminating such discrepancies through the implementation of a phased-in work plan that will examine the impact associated with the adoption of ICH guidances. This will result in the amendment or, depending on the extent of revisions required, withdrawal of some Health Canada guidances.
Should you have any questions or comments regarding the content of the guidance, please contact:
BPS Enquiries - Bureau of Pharmaceutical Sciences
This guidance has been developed by the appropriate ICH Expert Working Group and has been subject to consultation by the regulatory parties, in accordance with the ICH Process. The ICH Steering Committee has endorsed the final draft and recommended its adoption by the regulatory bodies of the European Union, Japan and the United States of America.
In adopting this ICH guidance, Health Canada endorses the principles and practices described therein. This document should be read in conjunction with the accompanying notice and the relevant sections of other applicable guidances.
Guidance documents are meant to provide assistance to industry and health care professionals on how to comply with the policies and governing statutes and regulations. They also serve to provide review and compliance guidance to staff, thereby ensuring that mandates are implemented in a fair, consistent and effective manner.
Guidance documents are administrative instruments not having force of law and, as such, allow for flexibility in approach. Alternate approaches to the principles and practices described in this document may be acceptable provided they are supported by adequate scientific justification. Alternate approaches should be discussed in advance with the relevant program area to avoid the possible finding that applicable statutory or regulatory requirements have not been met.
As a corollary to the above, it is equally important to note that Health Canada reserves the right to request information or material, or define conditions not specifically described in this guidance, in order to allow the Department to adequately assess the safety, efficacy or quality of a therapeutic product. Health Canada is committed to ensuring that such requests are justifiable and that decisions are clearly documented.
|Q10||Approval by the Steering Committee under Step 2 and release for public consultation.||9 May 2007|
|Q10||Approval by the Steering Committee under Step 4 and recommendation for adoption to the three ICH regulatory bodies.||4 June 2008|
Table of Contents
- 1. Pharmaceutical Quality System
- 1.1 Introduction
- 1.2 Scope
- 1.3 Relationship of ICH Q10 to Regional GMP Requirements, ISO Standards and ICH Q7
- 1.4 Relationship of ICH Q10 to Regulatory Approaches
- 1.5 ICH Q10 Objectives
- 1.6 Enablers: Knowledge Management and Quality Risk Management
- 1.7 Design and Content Considerations
- 1.8 Quality Manual
- 2. Management Responsibility
- 3. Continual Improvement of Process Performance and Product Quality
- 3.1 Lifecycle Stage Goals
- 3.2 Pharmaceutical Quality System Elements
- 4. Continual Improvement of the Pharmaceutical Quality System
- 5. Glossary
1. Pharmaceutical Quality System
This document establishes a new ICH tripartite guideline describing a model for an effective quality management system for the pharmaceutical industry, referred to as the Pharmaceutical Quality System. Throughout this guideline, the term "pharmaceutical quality system" refers to the ICH Q10 model.
ICH Q10 describes one comprehensive model for an effective pharmaceutical quality system that is based on International Standards Organisation (ISO) quality concepts, includes applicable Good Manufacturing Practice (GMP) regulations and complements ICH Q8 "Pharmaceutical Development" and ICH Q9 "Quality Risk Management". ICH Q10 is a model for a pharmaceutical quality system that can be implemented throughout the different stages of a product lifecycle. Much of the content of ICH Q10 applicable to manufacturing sites is currently specified by regional GMP requirements. ICH Q10 is not intended to create any new expectations beyond current regulatory requirements. Consequently, the content of ICH Q10 that is additional to current regional GMP requirements is optional.
ICH Q10 demonstrates industry and regulatory authorities' support of an effective pharmaceutical quality system to enhance the quality and availability of medicines around the world in the interest of public health. Implementation of ICH Q10 throughout the product lifecycle should facilitate innovation and continual improvement and strengthen the link between pharmaceutical development and manufacturing activities.
This guideline applies to the systems supporting the development and manufacture of pharmaceutical drug substances [ that is (i.e.), API ] and drug products, including biotechnology and biological products, throughout the product lifecycle.
The elements of ICH Q10 should be applied in a manner that is appropriate and proportionate to each of the product lifecycle stages, recognising the differences among, and the different goals of each stage (see Section 3).
For the purposes of this guideline, the product lifecycle includes the following technical activities for new and existing products:
- Pharmaceutical Development:
- Drug substance development;
- Formulation development (including container/closure system);
- Manufacture of investigational products;
- Delivery system development (where relevant);
- Manufacturing process development and scale-up;
- Analytical method development.
- Technology Transfer:
- New product transfers during Development through Manufacturing;
- Transfers within or between manufacturing and testing sites for marketed products.
- Commercial Manufacturing:
- Acquisition and control of materials;
- Provision of facilities, utilities, and equipment;
- Production (including packaging and labelling);
- Quality control and assurance;
- Distribution (excluding wholesaler activities).
- Product Discontinuation:
- Retention of documentation;
- Sample retention;
- Continued product assessment and reporting.
1.3 Relationship of ICH Q10 to Regional GMP Requirements, ISO Standards and ICH Q7
Regional GMP requirements, the ICH Q7 Guideline, "Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients", and ISO quality management system guidelines form the foundation for ICH Q10. To meet the objectives described below, ICH Q10 augments GMPs by describing specific quality system elements and management responsibilities. ICH Q10 provides a harmonised model for a pharmaceutical quality system throughout the lifecycle of a product and is intended to be used together with regional GMP requirements.
The regional GMPs do not explicitly address all stages of the product lifecycle [ for example (e.g.), Development ]. The quality system elements and management responsibilities described in this guideline are intended to encourage the use of science and risk based approaches at each lifecycle stage, thereby promoting continual improvement across the entire product lifecycle.
1.4 Relationship of ICH Q10 to Regulatory Approaches
Regulatory approaches for a specific product or manufacturing facility should be commensurate with the level of product and process understanding, the results of quality risk management, and the effectiveness of the pharmaceutical quality system. When implemented, the effectiveness of the pharmaceutical quality system can normally be evaluated during a regulatory inspection at the manufacturing site. Potential opportunities to enhance science and risk based regulatory approaches are identified in Annex 1. Regulatory processes will be determined by region.
1.5 ICH Q10 Objectives
Implementation of the Q10 model should result in achievement of three main objectives which complement or enhance regional GMP requirements.
1.5.1 Achieve Product Realisation
To establish, implement and maintain a system that allows the delivery of products with the quality attributes appropriate to meet the needs of patients, health care professionals, regulatory authorities (including compliance with approved regulatory filings) and other internal and external customers.
1.5.2 Establish and Maintain a State of Control
To develop and use effective monitoring and control systems for process performance and product quality, thereby providing assurance of continued suitability and capability of processes. Quality risk management can be useful in identifying the monitoring and control systems.
1.5.3 Facilitate Continual Improvement
To identify and implement appropriate product quality improvements, process improvements, variability reduction, innovations and pharmaceutical quality system enhancements, thereby increasing the ability to fulfil quality needs consistently. Quality risk management can be useful for identifying and prioritising areas for continual improvement.
1.6 Enablers: Knowledge Management and Quality Risk Management
Use of knowledge management and quality risk management will enable a company to implement ICH Q10 effectively and successfully. These enablers will facilitate achievement of the objectives described in Section 1.5 above by providing the means for science and risk based decisions related to product quality.
1.6.1 Knowledge Management
Product and process knowledge should be managed from development through the commercial life of the product up to and including product discontinuation. For example, development activities using scientific approaches provide knowledge for product and process understanding. Knowledge management is a systematic approach to acquiring, analysing, storing and disseminating information related to products, manufacturing processes and components. Sources of knowledge include, but are not limited to prior knowledge (public domain or internally documented); pharmaceutical development studies; technology transfer activities; process validation studies over the product lifecycle; manufacturing experience; innovation; continual improvement; and change management activities.
1.6.2 Quality Risk Management
Quality risk management is integral to an effective pharmaceutical quality system. It can provide a proactive approach to identifying, scientifically evaluating and controlling potential risks to quality. It facilitates continual improvement of process performance and product quality throughout the product lifecycle. ICH Q9 provides principles and examples of tools for quality risk management that can be applied to different aspects of pharmaceutical quality.
1.7 Design and Content Considerations
- The design, organisation and documentation of the pharmaceutical quality system should be well structured and clear to facilitate common understanding and consistent application.
- The elements of ICH Q10 should be applied in a manner that is appropriate and proportionate to each of the product lifecycle stages, recognising the different goals and knowledge available for each stage.
- The size and complexity of the company's activities should be taken into consideration when developing a new pharmaceutical quality system or modifying an existing one. The design of the pharmaceutical quality system should incorporate appropriate risk management principles. While some aspects of the pharmaceutical quality system can be company-wide and others site-specific, the effectiveness of the pharmaceutical quality system is normally demonstrated at the site level.
- The pharmaceutical quality system should include appropriate processes, resources and responsibilities to provide assurance of the quality of outsourced activities and purchased materials as described in Section 2.7.
- Management responsibilities, as described in Section 2, should be identified within the pharmaceutical quality system.
- The pharmaceutical quality system should include the following elements, as described in Section 3: process performance and product quality monitoring, corrective and preventive action, change management and management review.
- Performance indicators, as described in Section 4, should be identified and used to monitor the effectiveness of processes within the pharmaceutical quality system.
1.8 Quality Manual
A Quality Manual or equivalent documentation approach should be established and should contain the description of the pharmaceutical quality system. The description should include:
- The quality policy (see Section 2);
- The scope of the pharmaceutical quality system;
- Identification of the pharmaceutical quality system processes, as well as their sequences, linkages and interdependencies. Process maps and flow charts can be useful tools to facilitate depicting pharmaceutical quality system processes in a visual manner;
- Management responsibilities within the pharmaceutical quality system (see Section 2).
2. MANAGEMENT RESPONSIBILITY
Leadership is essential to establish and maintain a company-wide commitment to quality and for the performance of the pharmaceutical quality system.
2.1 Management Commitment
- Senior management has the ultimate responsibility to ensure an effective pharmaceutical quality system is in place to achieve the quality objectives, and that roles, responsibilities, and authorities are defined, communicated and implemented throughout the company.
- Management should:
- Participate in the design, implementation, monitoring and maintenance of an effective pharmaceutical quality system;
- Demonstrate strong and visible support for the pharmaceutical quality system and ensure its implementation throughout their organisation;
- Ensure a timely and effective communication and escalation process exists to raise quality issues to the appropriate levels of management;
- Define individual and collective roles, responsibilities, authorities and inter-relationships of all organisational units related to the pharmaceutical quality system. Ensure these interactions are communicated and understood at all levels of the organisation. An independent quality unit/structure with authority to fulfil certain pharmaceutical quality system responsibilities is required by regional regulations;
- Conduct management reviews of process performance and product quality and of the pharmaceutical quality system;
- Advocate continual improvement;
- Commit appropriate resources.
2.2 Quality Policy
- Senior management should establish a quality policy that describes the overall intentions and direction of the company related to quality.
- The quality policy should include an expectation to comply with applicable regulatory requirements and should facilitate continual improvement of the pharmaceutical quality system.
- The quality policy should be communicated to and understood by personnel at all levels in the company.
- The quality policy should be reviewed periodically for continuing effectiveness.
2.3 Quality Planning
- Senior management should ensure the quality objectives needed to implement the quality policy are defined and communicated.
- Quality objectives should be supported by all relevant levels of the company.
- Quality objectives should align with the company's strategies and be consistent with the quality policy.
- Management should provide the appropriate resources and training to achieve the quality objectives.
- Performance indicators that measure progress against quality objectives should be established, monitored, communicated regularly and acted upon as appropriate as described in Section 4.1 of this document.
2.4 Resource Management
- Management should determine and provide adequate and appropriate resources (human, financial, materials, facilities and equipment) to implement and maintain the pharmaceutical quality system and continually improve its effectiveness.
- Management should ensure that resources are appropriately applied to a specific product, process or site.
2.5 Internal Communication
- Management should ensure appropriate communication processes are established and implemented within the organisation.
- Communications processes should ensure the flow of appropriate information between all levels of the company.
- Communication processes should ensure the appropriate and timely escalation of certain product quality and pharmaceutical quality system issues.
2.6 Management Review
- Senior management should be responsible for pharmaceutical quality system governance through management review to ensure its continuing suitability and effectiveness.
- Management should assess the conclusions of periodic reviews of process performance and product quality and of the pharmaceutical quality system, as described in Sections 3 and 4.
2.7 Management of Outsourced Activities and Purchased Materials
The pharmaceutical quality system, including the management responsibilities described in this section, extends to the control and review of any outsourced activities and quality of purchased materials. The pharmaceutical company is ultimately responsible to ensure processes are in place to assure the control of outsourced activities and quality of purchased materials. These processes should incorporate quality risk management and include:
- Assessing prior to outsourcing operations or selecting material suppliers, the suitability and competence of the other party to carry out the activity or provide the material using a defined supply chain (e.g., audits, material evaluations, qualification);
- Defining the responsibilities and communication processes for quality-related activities of the involved parties. For outsourced activities, this should be included in a written agreement between the contract giver and contract acceptor;
- Monitoring and review of the performance of the contract acceptor or the quality of the material from the provider, and the identification and implementation of any needed improvements;
- Monitoring incoming ingredients and materials to ensure they are from approved sources using the agreed supply chain.
2.8 Management of Change in Product Ownership
When product ownership changes, (e.g., through acquisitions) management should consider the complexity of this and ensure:
- The ongoing responsibilities are defined for each company involved;
- The necessary information is transferred.
3. Continual Improvement of Process Performance and Product Quality
This section describes the lifecycle stage goals and the four specific pharmaceutical quality system elements that augment regional requirements to achieve the ICH Q10 objectives, as defined in Section 1.5. It does not restate all regional GMP requirements.
3.1 Lifecycle Stage Goals
The goals of each product lifecycle stage are described below.
3.1.1 Pharmaceutical Development
The goal of pharmaceutical development activities is to design a product and its manufacturing process to consistently deliver the intended performance and meet the needs of patients and healthcare professionals, and regulatory authorities and internal customers' requirements. Approaches to pharmaceutical development are described in ICH Q8. The results of exploratory and clinical development studies, while outside the scope of this guidance, are inputs to pharmaceutical development.
3.1.2 Technology Transfer
The goal of technology transfer activities is to transfer product and process knowledge between development and manufacturing, and within or between manufacturing sites to achieve product realisation. This knowledge forms the basis for the manufacturing process, control strategy, process validation approach and ongoing continual improvement.
3.1.3 Commercial Manufacturing
The goals of manufacturing activities include achieving product realisation, establishing and maintaining a state of control and facilitating continual improvement. The pharmaceutical quality system should assure that the desired product quality is routinely met, suitable process performance is achieved, the set of controls are appropriate, improvement opportunities are identified and evaluated, and the body of knowledge is continually expanded.
3.1.4 Product Discontinuation
The goal of product discontinuation activities is to manage the terminal stage of the product lifecycle effectively. For product discontinuation, a pre-defined approach should be used to manage activities such as retention of documentation and samples and continued product assessment (e.g., complaint handling and stability) and reporting in accordance with regulatory requirements.
3.2 Pharmaceutical Quality System Elements
The elements described below might be, required in part under regional GMP regulations. However, the Q10 model's intent is to enhance these elements in order to promote the lifecycle approach to product quality. These four elements are:
- Process performance and product quality monitoring system;
- Corrective action and preventive action (CAPA) system;
- Change management system;
- Management review of process performance and product quality.
These elements should be applied in a manner that is appropriate and proportionate to each of the product lifecycle stages, recognising the differences among, and the different goals of, each stage. Throughout the product lifecycle, companies are encouraged to evaluate opportunities for innovative approaches to improve product quality.
Each element is followed by a table of example applications of the element to the stages of the pharmaceutical lifecycle.
3.2.1 Process Performance and Product Quality Monitoring System
Pharmaceutical companies should plan and execute a system for the monitoring of process performance and product quality to ensure a state of control is maintained. An effective monitoring system provides assurance of the continued capability of processes and controls to produce a product of desired quality and to identify areas for continual improvement. The process performance and product quality monitoring system should:
- Use quality risk management to establish the control strategy. This can include parameters and attributes related to drug substance and drug product materials and components, facility and equipment operating conditions, in-process controls, finished product specifications, and the associated methods and frequency of monitoring and control. The control strategy should facilitate timely feedback / feedforward and appropriate corrective action and preventive action;
- Provide the tools for measurement and analysis of parameters and attributes identified in the control strategy (e.g., data management and statistical tools);
- Analyse parameters and attributes identified in the control strategy to verify continued operation within a state of control;
- Identify sources of variation affecting process performance and product quality for potential continual improvement activities to reduce or control variation;
- Include feedback on product quality from both internal and external sources, e.g., complaints, product rejections, non-conformances, recalls, deviations, audits and regulatory inspections and findings;
- Provide knowledge to enhance process understanding, enrich the design space (where established), and enable innovative approaches to process validation.
|Pharmaceutical Development||Technology Transfer||Commercial Manufacturing||Product Discontinuation|
|Process and product knowledge generated and process and product monitoring conducted throughout development can be used to establish a control strategy for manufacturing.||Monitoring during scale-up activities can provide a preliminary indication of process performance and the successful integration into manufacturing. Knowledge obtained during transfer and scale up activities can be useful in further developing the control strategy.||A well-defined system for process performance and product quality monitoring should be applied to assure performance within a state of control and to identify improvement areas.||Once manufacturing ceases, monitoring such as stability testing should continue to completion of the studies. Appropriate action on marketed product should continue to be executed according to regional regulations.|
3.2.2 Corrective Action and Preventive Action (CAPA) System
The pharmaceutical company should have a system for implementing corrective actions and preventive actions resulting from the investigation of complaints, product rejections, non-conformances, recalls, deviations, audits, regulatory inspections and findings, and trends from process performance and product quality monitoring. A structured approach to the investigation process should be used with the objective of determining the root cause. The level of effort, formality, and documentation of the investigation should be commensurate with the level of risk, in line with ICH Q9. CAPA methodology should result in product and process improvements and enhanced product and process understanding.
|Pharmaceutical Development||Technology Transfer||Commercial Manufacturing||Product Discontinuation|
|Product or process variability is explored. CAPA methodology is useful where corrective actions and preventive actions are incorporated into the iterative design and development process.||CAPA can be used as an effective system for feedback, feedforward and continual improvement.||CAPA should be used and the effectiveness of the actions should be evaluated.||CAPA should continue after the product is discontinued. The impact on product remaining on the market should be considered as well as other products which might be impacted.|
3.2.3 Change Management System
Innovation, continual improvement, the outputs of process performance and product quality monitoring and CAPA drive change. In order to evaluate, approve and implement these changes properly, a company should have an effective change management system. There is generally a difference in formality of change management processes prior to the initial regulatory submission and after submission, where changes to the regulatory filing might be required under regional requirements.
The change management system ensures continual improvement is undertaken in a timely and effective manner. It should provide a high degree of assurance there are no unintended consequences of the change.
The change management system should include the following, as appropriate for the stage of the lifecycle:
- Quality risk management should be utilised to evaluate proposed changes. The level of effort and formality of the evaluation should be commensurate with the level of risk;
- Proposed changes should be evaluated relative to the marketing authorisation, including design space, where established, and/or current product and process understanding. There should be an assessment to determine whether a change to the regulatory filing is required under regional requirements. As stated in ICH Q8, working within the design space is not considered a change (from a regulatory filing perspective). However, from a pharmaceutical quality system standpoint, all changes should be evaluated by a company's change management system;
- Proposed changes should be evaluated by expert teams contributing the appropriate expertise and knowledge from relevant areas (e.g., Pharmaceutical Development, Manufacturing, Quality, Regulatory Affairs and Medical), to ensure the change is technically justified. Prospective evaluation criteria for a proposed change should be set;
- After implementation, an evaluation of the change should be undertaken to confirm the change objectives were achieved and that there was no deleterious impact on product quality.
|Pharmaceutical Development||Technology Transfer||Commercial Manufacturing||Product Discontinuation|
|Change is an inherent part of the development process and should be documented; the formality of the change management process should be consistent with the stage of pharmaceutical development.||The change management system should provide management and documentation of adjustments made to the process during technology transfer activities.||A formal change management system should be in place for commercial manufacturing. Oversight by the quality unit should provide assurance of appropriate science and risk based assessments.||Any changes after product discontinuation should go through an appropriate change management system.|
3.2.4 Management Review of Process Performance and Product Quality
Management review should provide assurance that process performance and product quality are managed over the lifecycle. Depending on the size and complexity of the company, management review can be a series of reviews at various levels of management and should include a timely and effective communication and escalation process to raise appropriate quality issues to senior levels of management for review.
- a. The management review system should include:
- 1. The results of regulatory inspections and findings, audits and other assessments, and commitments made to regulatory authorities;
- 2. Periodic quality reviews, that can include:
- Measures of customer satisfaction such as product quality complaints and recalls;
- Conclusions of process performance and product quality monitoring;
- The effectiveness of process and product changes including those arising from corrective action and preventive actions.
- 3. Any follow-up actions from previous management reviews.
- b. The management review system should identify appropriate actions, such as:
- Improvements to manufacturing processes and products;
- Provision, training and/or realignment of resources;
- Capture and dissemination of knowledge.
|Pharmaceutical Development||Technology Transfer||Commercial Manufacturing||Product Discontinuation|
|Aspects of management review can be performed to ensure adequacy of the product and process design.||Aspects of management review should be performed to ensure the developed product and process can be manufactured at commercial scale.||Management review should be a structured system, as described above, and should support continual improvement.||Management review should include such items as product stability and product quality complaints.|
4 Continual Improvement of the Pharmaceutical Quality System
This section describes activities that should be conducted to manage and continually improve the pharmaceutical quality system.
4.1 Management Review of the Pharmaceutical Quality System
Management should have a formal process for reviewing the pharmaceutical quality system on a periodic basis. The review should include:
- Measurement of achievement of pharmaceutical quality system objectives;
- Assessment of performance indicators that can be used to monitor the effectiveness of processes within the pharmaceutical quality system, such as:
- Complaint, deviation, CAPA and change management processes;
- Feedback on outsourced activities;
- Self-assessment processes including risk assessments, trending, and audits;
- External assessments such as regulatory inspections and findings and customer audits.
4.2 Monitoring of Internal and External Factors Impacting the Pharmaceutical Quality System
Factors monitored by management can include:
- a. Emerging regulations, guidance and quality issues that can impact the Pharmaceutical Quality System;
- b. Innovations that might enhance the pharmaceutical quality system;
- c. Changes in business environment and objectives;
- d. Changes in product ownership.
4.3 Outcomes of Management Review and Monitoring
The outcome of management review of the pharmaceutical quality system and monitoring of internal and external factors can include:
- e. Improvements to the pharmaceutical quality system and related processes;
- f. Allocation or reallocation of resources and/or personnel training;
- g. Revisions to quality policy and quality objectives;
- h. Documentation and timely and effective communication of the results of the management review and actions, including escalation of appropriate issues to senior management.
ICH and ISO definitions are used in ICH Q10 where they exist. For the purpose of ICH Q10, where the words "requirement", "requirements" or "necessary" appear in an ISO definition, they do not necessarily reflect a regulatory requirement. The source of the definition is identified in parentheses after the definition. Where no appropriate ICH or ISO definition was available, an ICH Q10 definition was developed.
Potential Opportunities to Enhance Science and Risk Based Regulatory ApproachesFootnote 1
|1. Comply with GMPs||Compliance - status quo|
|2. Demonstrate effective pharmaceutical quality system, including effective use of quality risk management principles (e.g., ICH Q9 and ICH Q10).||Opportunity to:
|3. Demonstrate product and process understanding, including effective use of quality risk management principles (e.g., ICH Q8 and ICH Q9).||Opportunity to:
|4. Demonstrate effective pharmaceutical quality system and product and process understanding, including the use of quality risk management principles (e.g., ICH Q8, ICH Q9 and ICH Q10).||Opportunity to:
Figure 1: Diagram of the ICH Q10 Pharmaceutical Quality System Model
Arrow diagram from left to right indicating "Pharmaceutical Development" to "Technology Transfer" to "Commercial Manufacturing" to "Product Discontinuation".
There is a grey shading around "Technology Transfer" to "Product Discontinuation" with a right arrow underneath indicating "Investigational Products" pointing into "GMP".
Under this there is a grey shaded rectangle indicating "Management Responsibilities".
Under this there is a grey shaded box indicating PQS Elements which are: "Process Performance & Product Quality Monitoring System, Corrective Action/Preventive Action (CAPA) System, Change Management System, Management Review."
Under this are two grey shaded boxes indicating Enablers which are "Knowledge Management, Quality Risk Management".
This diagram illustrates the major features of the ICH Q10 Pharmaceutical Quality System (PQS) model. The PQS covers the entire lifecycle of a product including pharmaceutical development, technology transfer, commercial manufacturing, and product discontinuation as illustrated by the upper portion of the diagram. The PQS augments regional GMPs as illustrated in the diagram. The diagram also illustrates that regional GMPs apply to the manufacture of investigational products.
The next horizontal bar illustrates the importance of management responsibilities explained in Section 2 to all stages of the product lifecycle. The following horizontal bar lists the PQS elements which serve as the major pillars under the PQS model. These elements should be applied appropriately and proportionally to each lifecycle stage recognising opportunities to identify areas for continual improvement.
The bottom set of horizontal bars illustrates the enablers: knowledge management and quality risk management, which are applicable throughout the lifecycle stages. These enablers support the PQS goals of achieving product realisation, establishing and maintaining a state of control, and facilitating continual improvement.
- Date modified: