SMIMM1141U Chemical Process Development and Production of Active Pharmaceutical Ingredients (API)
The course is intended for drug development professionals with contact to chemical process development.
Basic conventions terms and definitions will be discussed. Focus will be placed on scale-up, process optimization, yield considerations, purification, validation, registration, and regulatory approval for new processes.
Various strategies to achieve a safe, more economical, and defensible process will be covered. Other topics to be covered include: Design of Experiments, route scouting, telescoping, 2nd generation processes, process monitoring, selection of appropriate in-process controls, process analytical technology (PAT), thermogravimetric analysis, reaction calorimetry, and differential scanning calorimetry.
Special topics are catalysis and stereochemistry
Further subjects are quality assurance, GLP and GMP considerations, Quality-by-Design (QbD), environmental considerations, life cycle management, emission limits and monitoring, resource consumption and CO2-emission, safety, hazard and operability, risk assessment and handling excessive reaction conditions.
Upon successful completion of the course, participants are expected to:
Knowledge
- The course will make the participants familiar with the terms, principles and methods used in developing a chemical process from discovery to routine manufacturing.
Skills
- The participants will be able to discuss different aspects and solutions to problems in a broad range covering scale-up, organization, planning, process monitoring, validation, life cycle management, registration, resource consumption, environmental and safety issues.
Competencies
The course provides a solid introduction to working in
process development. The successful participant will have the
necessary knowledge in the area to
- Closely interact with specialists and work as project leader where process development is a part of the project
- Identify and explain common risks and problems in process development
- Compute and critically apply various process metrics
The syllabus corresponds to about 200 pages in the textbook Practical Process Research and Development by Neal G. Anderson, Academic Press Inc., U.S., 2000. (ISBN 0-12-059475-7). In addition, 2-3 case studies reported in current journal articles will be subject to analysis. Lecture materials will be provided as handouts. Purchase of the textbook is optional; however, process chemists will find the text highly useful in their daily work.
• A relevant bachelor degree or equivalent
• A minimum of 2 years of relevant job experience
• Proficiency in English
Lectures are based upon a combination of selected material from the textbook, scientific papers and the lecturers' own work and experiences. The workshops encourage the participants to actively propose solutions to challenges that often occur during process development, based on relevant examples found in the current literature.
- Category
- Hours
- Exam
- 2
- Lectures
- 20
- Preparation
- 50
- Theory exercises
- 10
- Total
- 82
1 August 2013. Closed for applications.
- Credit
- 3 ECTS
- Type of assessment
- Written examination, 2 hours under invigilationExamination design: The examination consists of a multiple choice test and of 1-2 literate problems based on a case story.
- Aid
- All aids allowed
Certain pocket calculators are allowed.
- Marking scale
- 7-point grading scale
- Censorship form
- External censorship
- Exam period
- 21 October 2013 at 2-4 pm
Criteria for exam assesment
The grade 12 is given when the examinee
- gives a well structured presentation with a clear outline
providing exact and correct answers
- demonstrates aplomb comprehensive view and combines convincingly
the learned elements
- demonstrates with few unimportant deficits: Aplomb mastering of
relevant terms, principles and methods used for developing a
process from discovery to production.
The grade 7 is given when the examinee
- gives a coherent presentation providing understandable
unambiguous answers, the great majority of which should be correct
- documents a certain overview over the learned elements and with
minor deficits demonstrates a firm knowledge of relevant terms,
principles and methods used for developing a process from discovery
to production.
The grade 02 is given when the examinee
- gives a less structured presentation with less precise answers.
The overview is limited and the ability to combine learned elements
is limited
- only to a limited extent and with a number of deficits
demonstrates capability to handle relevant terms, principles and
methods used for developing a process from discovery to
production.
Course information
- Language
- English
- Course code
- SMIMM1141U
- Credit
- 3 ECTS
- Level
- Part Time Master
- Duration
- Placement
- Autumn
7-11 October 2013. Examination 21 October 2013 at 2-4 pm
- Schedule
- .
- Course capacity
- 32 participants
- Continuing and further education
- Price
- Part-time master’s students at Faculty of Health and Medical Sciences DKK 9,470, freelance students DKK 11,220, freelance students from non-EU/EEA countries DKK 13,500. An additional fee of DKK 600 for course materials and DKK 750 for lunch, coffee, etc. will be charged. Prices may be subject to change. The textbook must be purchased by the student (approx. DKK 500).
- Study board
- Study Board for Part-time Master’s Programmes of Pharmaceutical Sciences
Contracting department
- Department of Drug Design and Pharmacology
Course responsibles
- Fredrik Björkling (fb@sund.ku.dk)
Lecturers
List of lecturers may be subject to change.
Claus Ulrich Jessen, Novo Nordisk A/S
Lisbeth Kværnø, H. Lundbeck A/S
Michael J. Mealy, H. Lundbeck A/S
Hans Petersen, H. Lundbeck A/S
Michael Bech Sommer, Zacco A/S
Niels Østergaard, Cheminova A/S