Kursussøgning, efter- og videreuddannelse – Københavns Universitet

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Kursussøgning, efter- og videreuddannelse

Master's project

Practical information
Study year 2016/2017
Time
Autumn , Spring And Summer
Price

DKK 30,000 The fee covers supervision, evaluation of the master's project, administration, use of library facilities, etc.

Programme level Part Time Master
ECTS 12 ECTS
Course responsible
  • Lene Jørgensen (14-6f687168316d72756a68717668714376787167316e7831676e)
  • Department of Pharmacy
Course number: SMPMA0014E

Course content

The master's project typically comprises a literature study on a selected topic, selection and description of relevant regulations, guidelines literature and scientific based documentation, a discussion of the scientific based documentation related to the relevant literature, regulations and guidelines and a conclusion on the results of the project. The project topic can be an investigation of a particular regulatory case, implementation of a regulatory activity in a company, or a study of a particular regulatory problem. In any event, the selected subject should be put into the context of a broad regulatory perspective.

Project work should preferably be conducted at the student's workplace. If that is not possible, the Study Board will help the student with contacts to a relevant place of study. The written report will be supervised by at least one teacher from The Faculty of Health and Medical Sciences (Faculty supervisor) and preferably also by an employee from the company or institution hosting the master's project (external supervisor).

Before commencing the master's project, the student should sign a master's project agreement. The master's project agreement should be send by email to master@sund.ku.dk.

The company at which the project is conducted may require a declaration of confidentiality by the student, supervisors and potentially also the external examiner. In this event, the master's project is confidential.

Master’s projects can be carried out in groups of no more than two students. Any group work must be approved by the supervisor as a part of the master's project agreement. If a Master’s project is written by a group of students, the oral examination must be individual and the student may only attend the examination of the other students in the group if his or her examination has been held.

Half-way through the project, the student is encouraged to make an oral presentation (approx. 30 min.) on project status, a so-called mid-term assessment, to the supervisors and other relevant persons.

The master's project must be written in English. The final oral examination is usually conducted in English, but may be conducted in Danish, if the examinee, examiner and external examiner agree.

All master’s projects must have an abstract in English (compulsary) and may include an abstract in Danish (optional). The abstract must be maximum one A4 page. The abstract must summarize the research question, the methods used, important findings, a discussion if relevant, and a conclusion. The abstract will be included in the overall assessment of the master's project.

The cover page of the master’s project must include the title in English, and subtitle if relevant, the student’s name, study programme, the year, the name or names of supervisor/s, department but not the student’s civil registration (CPR) number. The master’s project is handed in to the Faculty supervisor in four copies.

Learning outcome

The written master’s report on the work conducted plus the subsequent oral examination must document that the student is able:

  • To plan and carry out a practice-oriented research project that can help strengthens part of pharmaceutical regulatory affairs
  • To formulate a regulatory research question/hypothesis
  • To write a statement of purpose
  • To use relevant regulations, guidelines, theory and scientific documentations when conducting a regulatory research project and to justify the choices made
  • To describe the regulatory research work conducted as well as the results achieved and conclusions in a way that is clear and understandable
  • To make a critical analysis with a balanced discussion of the described regulatory research and results
  • To make an oral presentation and discussion of the completed project.

Mandatory prerequisites

It is recommended for students to have passed compulsory courses equivalent to at least 20 ECTS credits before commencing the master's project. The Faculty supervisor may require documentation (a transcript of the university's Examination Register) showing that the student has passed, or is enrolled in, certain compulsory and elective courses (up to a maximum of 7.5 ECTS credits) before commencing the master's project.

Remarks

The student can choose the credit size of the master project. The credits of the master project must be between 12 ECTS and 20 ECTS.

Sign up

Before commencing the master's project, the student should contact a relevant Faculty supervisor to make a master's project agreement. The student must send a copy of the master's project agreement to master@sund.ku.dk.

Education

Master of Pharmaceutical Regulatory Affairs

Studyboard

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

Course type

Part time Master and Diploma courses

Teacher

The project supervisor is also course administrator and is responsible for ensuring the academic content of the project.

Duration

Schedulegroup

Placement and Schedule is established in the master's project agreement
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Teaching and learning methods

Individually supervised project work.

Language

English

Workload

Category Hours
Project work 330
Guidance 15
Exam 1
English 346

Exam

Type of assessment

Written assignment, Approximately 6 months
Oral defence, Approximately 1 1/2 hour
Written report (25-40 pages). The oral defence (approximately 1 1/2 hours) consists of an oral presentation of approximately 20-30 minutes and subsequent discussion.

Aid

All aids allowed

Marking scale

7-point grading scale

Criteria for exam assessment

Grade 12 is given for an excellent project showing high-level command of all aspects of the project topic, with no or only a few minor weaknesses.

Grade 7 is given for a good project displaying good command of the project topic, with some weaknesses.

Grade 02 is given for a project meeting only the minimum requirements for acceptance

Censorship form

External censorship
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