Study-Unit Description

Study-Unit Description


CODE PHR5008

 
TITLE Specialisation in Industrial Pharmacy

 
UM LEVEL 05 - Postgraduate Modular Diploma or Degree Course

 
MQF LEVEL 7

 
ECTS CREDITS 20

 
DEPARTMENT Pharmacy

 
DESCRIPTION - Comprehensive approach to industrial pharmacy
- Understanding of current issues relating to industrial pharmacy
- Integration of skills, concepts and knowledge base to industrial pharmacy
- Pharmaceutical development processes

Study-unit Aims:

- To provide flexibility to allow students to specialise in industrial pharmacy;
- To present science-based principles related to processes and regulations in the pharmaceutical industry.

Learning Outcomes:

1. Knowledge & Understanding
By the end of the study-unit the student will be able to:

- Apply scientific knowledge to processes within the pharmaceutical industry;
- Scientifically assess issues related industrial pharmacy.

2. Skills
By the end of the study-unit the student will be able to:

- Identify processes related to pharmaceutical manufacturing;
- Comprehend issues related to the industrial pharmacy.

Main Text/s and any supplementary readings:

- Beaney AM. Quality Assurance of Aseptic Preparation Services. UK: Pharmaceutical Press, 2005.
- Chamberlain J. Analysis of Drugs in Biological Fluids. UK: CRC, 1995.
- Gibson M. Pharmacy preformulation and formulation. USA: Interpharm Press, 2001.
- Harman RJ. Development and Control of Medicines and Medical Devices. UK: Pharmaceutical Press, 2004.
- Moffat AC, Osselton MD, Widdop B. Clarke’s Analysis of Drugs and Poisons. UK: Pharmaceutical Press, 2003.
- Podczeck F, Jones BE. Pharmaceutical Capsules. UK: Pharmaceutical Press, 2004.
- Rang HP. Drug Discovery and Development. USA: Churchill Livingstone, 2006.
- Rowe RC, Sheskey PJ, Owen SC. Handbook of Pharmaceutical Excipients. UK: Pharmaceutical Press & American Pharmacists Association, 2005.
- Sharp J. Quality in the Manufacture of Medicines and other Healthcare Products. UK: Pharmaceutical Press, 2000.
- Swartz ME, Krall IS. Analytical Regulatory and Validation Compliance. UK: Marcel Dekker, 1997.
- Wachter AH, Nash RA, Swarbrick J. Pharmaceutical Process Validation. UK: Marcel Dekker, 2003.

 
STUDY-UNIT TYPE Lecture and Tutorial

 
METHOD OF ASSESSMENT
Assessment Component/s Assessment Due Sept. Asst Session Weighting
Examination (6 Hours) See note below Yes 100%
Note: Assessment due date will be notified by the Faculty/Institute/Centre/School.

 
LECTURER/S Lilian M. Azzopardi
Nicolette Sammut Bartolo
Anthony Serracino Inglott

 

 
The University makes every effort to ensure that the published Courses Plans, Programmes of Study and Study-Unit information are complete and up-to-date at the time of publication. The University reserves the right to make changes in case errors are detected after publication.
The availability of optional units may be subject to timetabling constraints.
Units not attracting a sufficient number of registrations may be withdrawn without notice.
It should be noted that all the information in the description above applies to study-units available during the academic year 2023/4. It may be subject to change in subsequent years.

https://www.um.edu.mt/course/studyunit