Clinical Trials Toxicology
Undergraduate
Undergraduate
MEDI 4016
Undergraduate
No
171338
4.5
No
UniSA Clinical & Health Sciences
To provide an in-depth knowledge of the toxicities associated with drug development, including processes of discovery, design, development, preclinical testing and clinical trials of novel drugs.
Overview the need, procedures and processes involved in drug design and development for clinical trials; provide specific examples of where toxicology issues can arise; developing compounds to act on a target and identifying potential off-target interactions of compounds and the specific toxic effects that may arise; regulated manufacturing of compounds; pre-clinical studies (including high-throughput screening and animal models) focussing on safety; research ethics (animal and human) and the importance of monitoring and reporting; moving from pre-clinical to clinical trials and safety approvals required; importance of capturing toxicity data from clinical trials.
Nil
Common to all relevant programs | |
---|---|
Subject Area & Catalogue Number | Course Name |
BIOL 2035 | Physiology |
Nil
Component | Duration | ||
---|---|---|---|
INTERNAL, CITY WEST (INTENSIVE) | |||
Online | - x 13 weeks | ||
Workshop | 2 hours x 13 weeks | ||
Practical | 3 hours x 6 weeks | ||
Seminar | 4 hours x 2 weeks | ||
INTERNAL, CITY EAST (INTENSIVE) | |||
Online | - x 13 weeks | ||
Workshop | 2 hours x 13 weeks | ||
Practical | 3 hours x 6 weeks | ||
Seminar | 4 hours x 2 weeks |
Note: These components may or may not be scheduled in every study period. Please refer to the timetable for further details.
Presentation, Report, Test/Quiz
EFTSL*: 0.125
Commonwealth Supported program (Band 2)
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Fee-paying program for domestic and international students
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Non-award enrolment
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* Equivalent Full Time Study Load. Please note: all EFTSL values are published and calculated at ten decimal places. Values are displayed to three decimal places for ease of interpretation.