Quality by Design (QbD) in Pharmaceutical Development
Course content
Quality by Design (QbD) is at the very heart of modern pharmaceutical development. The implementation of QbD principles provides cost-efficient approach for delivering high quality medicines for patients. Regulatory authorities - both the European Medicines Agency (EMA) and the U.S. Food and Drug Administration (FDA) - are placing great emphasis on the QbD component as a part of regulatory filing. QbD has become a crucial element of a stream-lined drug development process.
This course will provide an insight into the key principles of
QbD covering quality risk management, formal experimental design
and process analytical technology (PAT). Leading QbD experts – from
industry, regulatory and academic side – will introduce the current
knowledge on QbD and provide participants with ideas how this
knowledge can be implemented in your company. The course includes
practical demonstrations.
The course will provide a thorough introduction to the underlying principles and tools required for QbD-based pharmaceutical development and manufacturing:
- Basic risk analysis techniques
- Constructing the quality target product profile (QTPP)
- Identification of critical quality attributes (CQAs) and critical process parameters (CPPs)
- Design of Experiments (DoE): Basic screening designs, expanded designs
- Process Analytical Technologies (PAT): basic principles of chemometrics, purpose of process measurements in pharmaceutical development and manufacturing, examples of process measurement techniques
- Risk based regulatory framework.
Master of Industrial Drug
Development (MIND) - elective
The course is preapproved as an elective in the
Master Medicines Regulatory
Affairs (MRA) programme and open for freelance students
who meet the admission criteria. Students who gain admission
to courses will receive an invoice and an admission letter.
The course is intended as continuing professional development (CPD)
for professionals in the pharmaceutical industry, particularly in
production, regulatory affairs and quality functions. The course
will be an excellent introduction for those less familiar with QbD
and will provide those with more experience on QbD with new ideas
on how to further implement the company’s QbD
programme.
After completing the course the student must have gained the
following knowledge, skills and competencies:
Knowledge
- summarize the principles of the QbD approach in pharmaceutical development and manufacturing
- demonstrate basic knowledge about risk management, design of experiments and PAT
- demonstrate basic knowledge about the relationship of the QbD approach into design space and further, into the regulatory framework
Skills
- apply basic risk analysis and design of experiments techniques into practical cases
-
identify and suggest suitable process analytical tools for a given manufacturing environment
Competencies
- work in a multidisciplinary risk management team
- plan and implement basic design of experiments (DoE) approach
-
suggest a QbD approach for constructing a design space.
The course is organized as an intensive 5-day course and comprises lectures, group discussions, presentations and discussions. In order to emphasize the flow of the process, the course is to a large extent based on the use of cases in both lectures and assignments.
The common course syllabus is a collection of legislation, presentations (hand-outs) and cases, approx. 300 pages.
Applicants must meet the following criteria:
• A relevant bachelor degree or equivalent
• A minimum of 2 years of relevant job experience
• Proficiency in English
- ECTS
- 3 ECTS
- Type of assessment
-
Written assignment
- Type of assessment details
- An essay based on a selected QbD case and the common course syllabus. The essay must be 8-15 pages.
- Exam registration requirements
-
Active participation in the course is a prerequisite for assessment.
- Aid
- All aids allowed
- Marking scale
- passed/not passed
- Censorship form
- No external censorship
- Exam period
-
Deadline for submission of essay to be announced on the homepage of the MIND programme and MRA programme
- Re-exam
-
Announced on the homepage of the MIND programme and MRA programme
Criteria for exam assessment
To pass the exam, the participant must have written a comprehensive and structured report on a selected case in his/hers own words, which is based on relevant literature. This report should clearly demonstrate that the participant has gained:
Knowledge
- at basic level about risk management, design of experiments and PAT
Skills for
- applying basic risk analysis and design of experiments techniques into practical cases
-
identifying realistic process analytical tools for a given manufacturing environment
Competencies
- to work in a multidisciplinary risk management team
- to plan and implement basic design of experiments (DoE) approach
-
to suggest a QbD approach for constructing a design space.
Part time Master and Diploma courses
- Category
- Hours
- Class Instruction
- 40
- Preparation
- 22,5
- Exam
- 20
- English
- 82,5
Kursusinformation
- Language
- English
- Course number
- SMIMA1091U
- ECTS
- 3 ECTS
- Programme level
- Part Time Master
- Duration
-
5 days
- Placement
- Summer
- Price
-
See course fee details at programme webpage
- Schedulegroup
-
August 2023
- Capacity
- 25 participants
- Studyboard
- Study Board for the Professionel Master´s Degree Programmes at The Faculty og Health and Medical Science
Contracting department
- Department of Pharmacy
Contracting faculty
- Faculty of Health and Medical Sciences
Course Coordinator
- Jukka Rantanen (14-6c776d6d633074637076637067704275777066306d7730666d)
Teacher
Wim Oostra, PhD, Technical Manager, Abbott Healthcare, The
Netherlands
Øyvind Holte, PhD, Scientific officer, Norwegian Medicines Agency,
Norway
Erik Skibsted, PhD, Principal Scientist, Novo Nordisk A/S, Denmark
Additional speakers may be included.
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