Kursussøgning, efter- og videreuddannelse – Københavns Universitet

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Kursussøgning, efter- og videreuddannelse

Chemical Process Development and Production of Active Pharmaceutical Ingredients (API)

Practical information
Study year 2016/2017
Time
Autumn
14-18 November 2016
Price

DKK 12,900 (non-EU/EEA citizens DKK 15,051). Fee includes course materials and meals. Prices may be subject to change. Textbook must be purchased by the participants.

Programme level Part Time Master
ECTS 3 ECTS
Course responsible
  • Fredrik Björkling (2-68644275777066306d7730666d)
Course co-director Michael J. Mealy, H. Lundbeck A/S
  • Department of Drug Design and Pharmacology
Course number: SMIMM1141U

Course content

All relevant subjects related to the chemical process development of biologically active compounds used as pharmaceuticals will be discussed. The course will begin with the discovery synthesis and end with the full-scale production process.

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.

Examples of process developments will be given both for small molecular compounds and biopharmaceuticals.

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.

Learning outcome

The development of a safe and efficient manufacturing process of an active pharmaceutical ingredient (API) or bulk drug substance is a substantial undertaking. A successful endeavour requires solving problems within synthetic organic, bioorganic, physical organic, analytical and environmental chemistry, engineering, and economics. An understanding of chemical development and the particular challenges during each phase is the primary focus of this course. A combination of theory and practice using fresh examples from industry and the literature will create the foundation for solid decision-making skills and an understanding of the trade terminology.

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 or biological 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

Recommended prerequisites

It is necessary to understand a basic level of chemistry.

Mandatory prerequisites

Applicants must meet the following criteria:
• A relevant bachelor degree or equivalent
• A minimum of 2 years of relevant job experience
• Proficiency in English

Sign up

Application deadline 1 September 2016

Apply here

Education

Master's Programme in Industrial Drug Development - compulsory

Compulsory for Master of Industrial Drug Development (MIND) students, elective for other part-time master's students at the Faculty of Health and Medical Sciences (subject to study board approval) and open for freelance students who meet the admission criteria.

The course is intended for drug development professionals with contact to chemical process development.

Studyboard

Study Board for Part-time Master’s Programmes of Pharmaceutical Sciences

Course type

Part time Master and Diploma courses

Teacher

List of lecturers may be subject to change.

Michael J. Mealy, H. Lundbeck A/S
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

Duration

Schedulegroup

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Teaching and learning methods

The course is organized as an intensive 5-day course comprising lectures, workshops, plenary discussion and problem solving of real-life examples.

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.

Capacity

32 participants

Language

English

Literature

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.

Workload

Category Hours
Preparation 50
Lectures 20
Theory exercises 10
Exam 2
English 82

Exam (SMIMM1141E)

Type of assessment

Written examination, 2 hours under invigilation
Examination design: The examination consists of a multiple choice test and of 1-2 literate problems based on a case story.

Aid

All aids allowed

Apart from the standard programs and IT tools listed under The Faculty of Health and Medical Sciences at http://pc-exam.ku.dk/it_tools/health/ students will at this exam also have access to use a USB stick (for notes etc.)
 

Marking scale

7-point grading scale

Criteria for exam assessment

The examination will monitor the knowledge, skills and competences of the participants using the following criteria:

Knowledge

  • the understanding of the terms, principles and methods used in developing a chemical or biological process from discovery to routine manufacturing.


Skills

  • the ability 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 competence to identify and explain common risks and problems in process development
  • to compute and critically apply various process metrics

 

Censorship form

External censorship

Exam period

Announced on the MIND programme's webpage

Re-exam

Announced on the MIND programme's webpage

Mere information om kurset
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