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MSc PG Dip PG Cert Pharmaceutical Quality by Design

  • DeadlineStudy Details:

    MSc/PG Dip/PG Cert One year full-time

Course Description

Quality by Design (QbD) is based on the application of product and process sciences, from early-to-late stages of the product development cycle, to provide accelerated regulatory submission pathways for new drug applications.

  • This is the first MSc dedicated to the new QbD approach to pharmaceutical process and product development
  • Our established reputation of more than 104 years pharmacy teaching ensures we produce graduates of the highest calibre
  • It informs part of a major initiative, being driven and supported by the US, EU and Japanese regulatory authorities, and defined within the Q8, Q9 and Q10 Guidelines from the International Conference on Harmonization (ICH)
  • Our experienced practitioner and research based academic staff have recently received grant funded collaborative research and development to improve industrial process quality and efficiency, with the Technology Strategy Board, and Engineering and Physical Science Research Council
  • Benefit from our extensive funding and investment in our industry standard laboratories and specialist equipment
  • Our strong links, direct input and guest lectures from industrial experts ensure your learning is relevant to current practice and developments within the sector

 

Entry Requirements

A good Honours degree (minimum 2:2 or equivalent) in a chemical, biological or physical science, including (though not exclusive to) chemistry, biology, chemical engineering, engineering, pharmacy, pharmaceutical science, or physics (or equivalent)

Alternatively, we will accept a portfolio of professional and/or academic qualifications of equivalent standing to an Honours degree.

If English is not your first language an IELTS score of 6.5 or equivalent when you start the course is essential. English language tuition, delivered by our British Council accredited Centre for English Language Learning, is available both before and during the course if you need it.

To find out more, please visit dmu.ac.uk/international

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Fees

UK/EU:Full-time £5740. International: Full-time £12,500. Distance Learning 15 Credit module £980, 30 Credit module £1390, 60 Credit dissertation £2000

Module Details

The Pharmaceutical Quality by Design course will provide an understanding of the challenges faced by the pharmaceutical and healthcare industries (as they strive to develop new products) and equip you with modern product development and manufacturing solutions that conform to current industry best practices and modern QbD principles.

The course contains areas of core knowledge and skills with an emphasis on application of QbD principles and continuous improvement activities to the development and manufacture of pharmaceutical products. 180 credits must be completed to achieve a full master’s. The course has been structured to ensure you have a coherent and balanced programme of study in the following areas:

  • Principles and Practices of Quality by Design (15 credits)
    explores a variety of legislation and regulations relating to the quality of pharmaceutical products.


  • Product Design: Pre-formulation and Formulation (30 credits)
    introduces a variety of techniques and methods to formulate and produce safe medicines.

  • Analytical Techniques in Materials Science (15 credits)
    builds on the concept of materials science as a separate discipline.

  • Process Design, Control and Manufacturing (15 credits)
    considers the design, including facility, equipment, material transfer, and manufacturing variables using QbD principles.

  • Advances in Drug Delivery (15 credits)
    focuses on new therapeutic entities and delivery strategies. It is intended to integrate with ideas in other subject areas presented in the course, but also for the appreciation of future developments.

  • Biopharmaceuticals (15 credits)
    covers the use of large molecules, including those derived from biotechnology and especially those that are biologically active to produce therapeutic responses.


  • Process Analytical Technology and Chemometrics (15 credits)
    describes online process monitoring and the use of Process Analytical Technology (PAT) to advance pharmaceutical process identification, simulation and control.

  • Experimental Design and Research Methods (15 credits)
    focuses on research and experiment design methods applying QbD principles. The importance of design space concept will be discussed. Issues are primarily illustrated through examples from industrial cases.

Attendance: Expected to attend university full-time, up to 10 hours per week (please note this is subject to change)

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