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Master of Science Clinical Research in Regulatory Affairs

Master of Science Clinical Research in Regulatory Affairs

at University of Petroleum and Energy Studies India

Overview

Clinical Research enables health care professionals to develop new therapies and diagnostic procedures and medical devices to ensure better patient care. M.Sc. in Clinical Research is a 2-year postgraduate course aimed at providing experiential learning with comprehensive curriculum.

Regulatory Affairs is a domain with a broad overview and the responsibility for collecting all kinds of data from the development processes and sending it to regulatory authorities. The courses will provide broad perspectives and integrated knowledge to the students from Innovation →Discovery → Approval→ Commercialization which implies regulatory affairs are essential to bring the product to the market globally. This course specialization provides a comprehensive education in the important aspects of Regulatory and Quality compliance in pharmaceutical industry. Students gets updated with the current regulatory and compliance issues and explore careers in these exciting times. Nowadays regulations and ever changing laws are driving demand for pharmaceutical regulatory affair professionals who can help companies successfully bring medical products to the market.

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30

Application Processing Days

Under Graduate

Program Level

Fact & Figures

Full Time On Campus

Study Mode

24

Duration

University of Petroleum and Energy Studies

Location

Master of Science Clinical Research in Regulatory Affairs Assistant Fee

$128000

Tuition Fee

$NA

Average Cost of Living

$1300

Application Fee

Master of Science Clinical Research in Regulatory Affairs Admissions Requirements

  • X and XII With 50% and Graduation in any stream such as Life Sciences (Biochemistry, Pharmacology, Toxicology, Biotechnology, Microbiology, Botany or Zoology), M.B.B.S. / B.D.S. / B.A.M.S. / B.H.M.S./B.U.M.S. / BVSc. / B.S.S.M.), Bachelors in Physiotherapy, B. Pharmacy, Nursing with min 50%.
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Detailed Program and Facts

30

Application Processing Days

Full Time On Campus

Program Intensity

Under Graduate

Program Level

24

Duration

Study Visa

Clinical Research enables health care professionals to develop new therapies and diagnostic procedures and medical devices to ensure better patient care. M.Sc. in Clinical Research is a 2-year postgraduate course aimed at providing experiential learning with comprehensive curriculum.

Regulatory Affairs is a domain with a broad overview and the responsibility for collecting all kinds of data from the development processes and sending it to regulatory authorities. The courses will provide broad perspectives and integrated knowledge to the students from Innovation →Discovery → Approval→ Commercialization which implies regulatory affairs are essential to bring the product to the market globally. This course specialization provides a comprehensive education in the important aspects of Regulatory and Quality compliance in pharmaceutical industry. Students gets updated with the current regulatory and compliance issues and explore careers in these exciting times. Nowadays regulations and ever changing laws are driving demand for pharmaceutical regulatory affair professionals who can help companies successfully bring medical products to the market.

Other Courses by University of Petroleum and Energy Studies,India

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24 month

Duration

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24 month

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Tuition

Health Sciences, Nursing and Emergency Services

Master of Science Clinical Research in Regulatory Affairs

Clinical Research enables health care professionals to develop new therapies and diagnostic procedures and medical devices to ensure better patient care. M.Sc. in Clinical Research is a 2-year postgraduate course aimed at providing experiential learning with comprehensive curriculum.

Regulatory Affairs is a domain with a broad overview and the responsibility for collecting all kinds of data from the development processes and sending it to regulatory authorities. The courses will provide broad perspectives and integrated knowledge to the students from Innovation →Discovery → Approval→ Commercialization which implies regulatory affairs are essential to bring the product to the market globally. This course specialization provides a comprehensive education in the important aspects of Regulatory and Quality compliance in pharmaceutical industry. Students gets updated with the current regulatory and compliance issues and explore careers in these exciting times. Nowadays regulations and ever changing laws are driving demand for pharmaceutical regulatory affair professionals who can help companies successfully bring medical products to the market.

24 month

Duration

$ 128000

Tuition

Health Sciences, Nursing and Emergency Services

Bachelor of Technology in (Biotechnology)- Biosimilars

Biosimilar is that branch of study which deals with study of drugs that are very similar to original product, but not identical. They are not generic drugs and do not possess the same active pharmaceutical ingredient, yet comparable to original reference drug in terms of quality, safety and efficacy. Biosimilar are alternative potential therapeutics but not generics. For biosimilar products, the manufacturing process requires a high level of monitoring and testing.  

At UPES, B.Tech. Biotechnology students with a specialization in Biosimilar will be made familiar with existing regulations, manufacturing sciences and distribution practices of Biosimilar products in India and all across the globe. Students will learn about controversies associated with Generic drugs and need for development of Biosimilar products. Students will also learn how a drug is discovered in a lab, followed by testing in clinical trials and then launched in market for commercialization.

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Duration

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Duration

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View All Courses by University of Petroleum and Energy Studies, India

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