Turning QbD into a Practical Reality (T43)

Level: Fundamental
ISPE CEUs: 1.5
Type: Classroom Training Course
Primer Webinar

Description

Substantial business benefits are emerging from industry when Quality by Design (QbD) principles are used for new and existing drug products yielding reduced operating costs, enabling significantly more efficient manufacturing processes and better positioning companies to meet increasing regulatory expectations.

For example, the completion of ICH Guidelines, Q8 (R2): Pharmaceutical Development, Q9: Quality Risk Management and Q10: Pharmaceutical Quality System and the recent USFDA guidance on Process Validation contain recommendations for building and capturing process knowledge and understanding and establishing a strategy for process control during Stage 1, process design. There is evidence from 483s and warning letters that FDA is citing unacceptable levels of process understanding, like an unidentified and lack of control of factors that cause variability in process. Additionally, FDA appears to be accelerating the QbD push, suggesting that ANDAs for generic drugs should have QbD elements from 2013 onward. Regulatory expectations are increasing.

This interactive training course utilizes the ISPE PQLI Guide Series: Part 1 - Product Realization using Quality by Design, Concepts and Principles and Part 2 - Product Realization using Quality by Design, Illustrative Example as the basis for explaining and providing examples of how products and processes can be developed, using QbD with special emphasis on the considerations for implementing these processes in manufacturing.

Through group exercises the course will delve into implementation and operation of an effective and efficient control strategy in manufacturing which is a key element of process performance and product quality monitoring and continual improvement. The link to control of attributes and parameters to relevant critical quality attributes of the product and application and implementation of enhanced, QbD approaches and USFDA Process Validation Guidance will also be explored.

Note: This course will not cover the regulatory submission processes or detailed engineering designs.

Note: This course will not cover the regulatory submission processes or detailed engineering designs

Webinar 

We recommend participants complete the primer course webinar, PQLI 101 that provides the background for the origins of the ICH guidelines, Q8 (R2), Q9, Q10 and Q11: Development and manufacture of drug substances (chemical entities and biotechnological/biological entities) and understand the link between these and other relevant regulatory guidelines and the ISPE PQLI Guides. You will receive information via email on how to access the webinar one week prior to the start of the training event.

Course Modules

Day 1

1. Regulatory background and benefits of QbD
2. QbD roadmap – ICH Q8R2
   • Breakout - Understanding QbD process
3. Quality Risk Management (QRM) (process and tools e.g. FMEA, risk ranking)
   • Breakout - Learning about FMEA
4. Control Strategy 1 - Options, selection, elements.
   • Breakout - Application of FMEA to Control Strategy selection
5. PQS & GMP and link to CS
   • Breakout - PQS/GMP and relationship to Control Strategy

Day 2

1. Review of Day 1
2. Control Strategy 2 - Application in manufacturing including process controls, PAT
   • Break out - application of FMEA to Control Strategy implementation
3. Process Validation – US FDA, Stages 1, 2 and 3 including equipment qualification, use of ASTM E2500 & ISPE C&Q science-and risk-based approach and the European approach to Process Validation
   • Breakout - Process Validation
4. Continual Improvement (CI) – an introduction to statistical process monitoring, importance of understanding analytical variability
   • Breakout on CI
5. How to apply the QbD principles in your own organisation

Take Back to Your Job

Within the manufacturing environment:

• understand and apply QbD terminology including the principles of a science- and risk-based approach, the importance of product and process understanding and patient requirements
• use tools and techniques provided to understand the application of Quality Risk Management (QRM)
• understand the implications of relevant ICH, EMA, and FDA Guidelines
• learn about the QbD process
• review some QRM tools (FMEA, risk ranking) and apply FMEA to Control Strategy selection
• know the relationship between PQS and GMP and how they link to Control Strategy
• understand the considerations when implementing a control strategy derived from enhanced, QbD approaches
• review the scope of the US FDA Process Validation including equipment qualification, ASTM E2500 and the ISPE Commissioning and Qualification and the links to science- and risk-based approaches
• examine opportunities for continual improvement arising from application of statistical techniques

Attendance Suggested For

Manufacturing, engineering, quality and validation professionals with intermediate level experience in manufacturing, engineering, validation, quality control and assurance, technology transfer and those that are new to Quality by Design principles.

CPIP™ Technical Knowledge and Competency Elements

This course contains knowledge related to the CPIP™ technical knowledge competency elements Product Development, Process and Product Development, Facilities and Equipment, Production Systems, Regulatory Compliance and Quality Systems. For complete information concerning the knowledge elements or the CPIP Credential, please visit www.ISPE-PCC.org.

Community of Practice (COP)

This training course is of particular interest to existing and future members of the ISPE API, C&Q, CU, OSD, PAT, PPD, Sterile Communities of Practice (COPs).

Continuing Education Units  

ISPE will provide continuing education units (ISPE CEUs) for all North American seminars and courses, including educational programming at the ISPE Annual Meeting. CEUs are nationally recognized units of achievement designed for those individuals continuing their education in their chosen field or profession.

Delegates attending European seminars and courses will receive a Certificate of Attendance, as ISPE CEUs are currently not offered at European events. Verification of CEUs is based on attendance as well as satisfactory completion of all evaluation materials. Statements of credit will be sent via email within four weeks of evaluation materials. One hour of education programming equals 0.1 ISPE CEU credits.