国际学生入学条件
Acceptance to this Master's programme requires a first degree with Honours or equivalent (2: 2) in a relevant area such as Biological Sciences, Chemistry, Integrated Science, Chemical Engineering, Pharmacy, Pharmacology or Pharmaceutical Sciences.
For North American students a GPA of normally 2.5 and above on a scale of 4.0 is required, or equivalent.
Candidates with certain two year's work experience and a degree below the 2:2 will also be considered.
You will need to achieve an overall score of at least 6.0, with at least 5.5 in each of the four sub-tests (speaking, listening, reading, writing). Testing facilities are available at most British Council overseas offices. When you take the test, you should ask for a copy of your Test Report Form to be sent to the University.
TOEFL, for which you will need to score at least 80 on the internet-based test, with sub-tests not less than Speaking 20, Listening 17, Reading 18, Writing 17
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雅思考试总分
6.0
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雅思考试指南
- 雅思总分:6
- 托福网考总分:80
- 托福笔试总分:160
- 其他语言考试:The Pearson Test of English Academic (PTE-A), for which you will need to achieve an overall score of at least 55, with at least 51 in each of the four sub-tests
CRICOS代码:
申请截止日期: 请与IDP顾问联系以获取详细信息。
课程简介
该计划是独一无二的,因为它结合了包括制药科学和药物控制在内的制药技术研究。它旨在为您提供与药物科学学科相关的高级科学理论知识,并为您提供该领域实验室工作所需的技能。这些学科包括药物制剂的开发,尤其侧重于制药过程中使用的技术以及药物的开发和生产。这种重点导致对许可和监管所需的临床试验的过程和程序的重视。药物管制是该计划的重要组成部分。它包括药品法规,药品许可,药品测试和安全性。您将通过应用质量保证来了解结构化实施和检查标准中涉及的关键流程。您还将获得与药物供应链和药物警戒有关的知识并开发技能,包括安全和正确
This programme is unique as it combines the study of pharmaceutical technology, including pharmaceutical sciences, and medicines control. It has been designed to provide you with an advanced theoretical knowledge of sciences that are related to disciplines in pharmaceutical sciences, and give you the skills you need for laboratory work in this area. These disciplines include the development of pharmaceutical formulation, with particular emphasis on the technology used in the pharmaceutical process and the development and production of medicines. This focus leads to an emphasis on the processes and procedures for clinical trials that are needed for licensing and regulation. Medicines control is an important element of this programme. It encompasses drug regulations, drug licensing, drug testing, and safety. You will learn about the key processes involved in structured enforcement and inspection standards through the application of quality assurance. You will also gain knowledge and develop skills related to pharmaceutical supply chains and pharmacovigilance, including the safe and proper use of medicines. You'll also have opportunities for hands-on experience in applying analytical and characterisation techniques such as liquid chromatography (LC) and gas chromatography (GC) combined with tandem mass spectrometric (MS/MS) detection, X-ray diffraction, scanning electron microscopy and near-infrared (NIR), nuclear magnetic resonance (NMR) and Raman spectroscopy.
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