This module will be delivered via a one-hour lecture and a three-hour practical per week. . Students may be required to carry out assignments, give presentations and take multiple choice questions. Independent learning will be facilitated during the preparation of assignments, presentations and practicals.
Module Aim:
To understand the procedures in drug production from synthesis to finished product manufacture.
To develop analytical procedures for routine pharmaceutical analysis.
To understand drug registration requirements.
Learning Outcomes
On successful completion of this module the learner should be able to:
LO1
Understand the procedures in drug production from synthesis to finished product manufacture.
LO2
Develop analytical procedures for routine pharmaceutical analysis.
LO3
Understand drug registration requirements.
LO4
Validate existing drug manufacturing plant and instrumentation.
Pre-requisite learning
Module Recommendations
This is prior learning (or a practical skill) that is recommended before enrolment in this module.
No recommendations listed
Incompatible Modules
These are modules which have learning outcomes that are too similar to the learning outcomes of this module.
No incompatible modules listed
Co-requisite Modules
No Co-requisite modules listed
Requirements
This is prior learning (or a practical skill) that is mandatory before enrolment in this module is allowed.
No requirements listed
Module Content & Assessment
Indicative Content
No indicative content
Assessment Breakdown
%
Continuous Assessment
10.00%
Practical
20.00%
End of Module Formal Examination
70.00%
Continuous Assessment
Assessment Type
Assessment Description
Outcome addressed
% of total
Assessment Date
Short Answer Questions
Regular written examinations to evaluate student understanding of course content
1,2,3,4
10.00
n/a
No Project
Practical
Assessment Type
Assessment Description
Outcome addressed
% of total
Assessment Date
Practical/Skills Evaluation
Dissolution studies of rapid release and controlled-release medications. Formulation of simple emulsion and tablets Assessment of physical stability. Assay development. 16. Use of conductivity to determine solubility products of a number of sparingly-soluble drugs. 17. Extraction by Soxhlet apparatus of podophyllin from podophyllum rhizomes.
1,4
20.00
Sem 1 End
End of Module Formal Examination
Assessment Type
Assessment Description
Outcome addressed
% of total
Assessment Date
Formal Exam
Final year evaluation
1,2,3,4
70.00
End-of-Semester
SETU Carlow Campus reserves the right to alter the nature and timings of assessment