国际学生入学条件
A bachelors degree or equivalent from an accredited college or university.
To submit and complete your application you must upload a PDF file of your unofficial transcript directly to your online application Unofficial transcripts must be in English.
Please ensure that the scanned documents are readable and include all courses grades ie marks scores etc and credits completed to date The scanned documents should also include information about the institutions grading scale If admitted you will need to provide your official transcript For a transcript to be official it must be in a sealed envelope from the transferring college or university.
Other Documents -
Statement of purpose - 500 words minimum.
Letters of recommendation 2 or 3 for graduate programs.
Curriculum vitae CV Resume.
TOEFL IBT - 79 and a writing portion of 20
IELTS - 6.5 no band lower than 6
展开 IDP—雅思考试联合主办方
雅思考试总分
6.5
了解更多
雅思考试指南
- 雅思总分:6.5
- 托福网考总分:79
- 托福笔试总分:160
- 其他语言考试:PTE - 53
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
药物,生物制品和医疗器械监管事务理学硕士课程旨在培养具备高素质的毕业生,以管理创新和开发尖端科学和医学产品的公司的监管流程。推动对法规事务专业人员的需求,这些专业人员可以帮助公司有效地将医疗产品推向市场。为了使您能够有效地管理监管活动,东北大学专业研究学院提供了药品,生物制品和医疗器械监管事务理学硕士学位。这个独特的研究生学位旨在加深您对当前法规及其在药物,生物制剂和医疗器械产品的开发和商业化中的实际应用的理解。该计划中的法规事务课程将为您提供所需的综合知识和广泛见解有效地管理法规流程。从发现到商业化,该
The Master of Science in Regulatory Affairs program is designed to produce graduates who are highly qualified to manage the regulatory process for companies innovating and developing cutting edge products in science and medicine.<br>The global convergence of regulatory science, technology-driven business decision making, formation of public policies, and evolving regulations are driving demand for regulatory affairs professionals who can facilitate the processes involved in bringing highly regulated products to market. To prepare you to effectively manage regulatory activities, Northeastern University's College of Professional Studies offers the Master of Science in Regulatory Affairs. This unique graduate degree is STEM-designated, and is designed to deepen your understanding of the global compliance requirements for the development, marketing approval, and utilization of technically complex and highly regulated products, including food, drugs, biologics, and medical devices.<br><br>Potential career paths: Clinical Scientist, Clinical Researcher, Research Scientist (medical),Clinical Research Director<br>Public Health Administrator
展开