This module will be delivered via two one-hour lectures for twelve weeks and one two-hour practical for ten weeks. Students may be required to access the material via College networks in advance of the class and practicals to encourage active learning. To consolidate lectures and practicals, students will normally be required to carry out assignments, give presentations and answer multiple choice questions. Group and peer learning will be facilitated during the preparation of assignments, presentations and practicals. Any course-related issue or questions that may arise will be discussed at lectures.
Online demonstrations will illustrate the key concepts of the course and will be available throughout the year. Digital resources such as Youtube, Reusable learning objects and the National Digital Learning Repository will be used as practicable.
Module Aim:
To give the student an insight into the requirements of formulation and compounding in the modern pharmacy.
Learning Outcomes
On successful completion of this module the learner should be able to:
LO1
Discuss the procedures in drug production from synthesis to finished product manufacture.
LO2
Develop and test a range of products containing pharmaceutical actives.
LO3
Evaluate and discuss processes involved in drug manufacture and basic quality assurance
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.
Successful completion of year 1 or equivalent
Module Content & Assessment
Indicative Content
Oral dosage route
Comminution, mixing, compression, granulation
Insulins
Formulation, storage and labelling
Sterile dosage forms
Formulation, manufacture and quality control. Clean rooms.
Clinical trials
Clinical trials. Blind and double-blind trials, placebo effect
Pulmonary medications
Formulation and manufacture
Oral liquids
Composition, manufacture, stability evaluation
Stability & shelf-life
Aims, product specification, assay
Modified drug release
Coatings and films, matrices and ion-exchangers
Quality control
Evaluation of tablets, capsules, suppositories
Other dosage forms
Ophthalmic preparations. Enemas
Practical
Practicals will allow students to develop the required technical competencies, attitudes and behaviours as well as problem-solving abilities and group skills promote deep learning via investigation of a problem, application of prior knowledge and analysis of results thus generating new knowledge.
Assessment Breakdown
%
Continuous Assessment
10.00%
Practical
40.00%
End of Module Formal Examination
50.00%
Special Regulation
Students must achieve a minimum grade (35%) in both practical/CA and final exam.
Continuous Assessment
Assessment Type
Assessment Description
Outcome addressed
% of total
Assessment Date
Other
MCQ, assignments and practical work
1,2
10.00
n/a
No Project
Practical
Assessment Type
Assessment Description
Outcome addressed
% of total
Assessment Date
Practical/Skills Evaluation
Continuous assessment will take the form of practical reports, and specific assignments
1,2
40.00
n/a
End of Module Formal Examination
Assessment Type
Assessment Description
Outcome addressed
% of total
Assessment Date
Formal Exam
2 hour exam
1,3
50.00
End-of-Semester
SETU Carlow Campus reserves the right to alter the nature and timings of assessment