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Integrated Bachelor of Science- Master of Science Clinical Research in Clinical Pharmacokinetics

Integrated Bachelor of Science- Master of Science Clinical Research in Clinical Pharmacokinetics

at University of Petroleum and Energy Studies India

Overview

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.

In addition this program also offers Artificial Intelligence and Machine Learning (AIML) applications in Clinical Research to upgrade Medical and Health Science. Machine Learning Techniques like pre-trained deep learning models and convolutional neural networks (CNN) provides excellent opportunities for drug-development processes and makes clinical trial more intelligent.

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30

Application Processing Days

Under Graduate

Program Level

Fact & Figures

Full Time On Campus

Study Mode

48

Duration

University of Petroleum and Energy Studies

Location

Integrated Bachelor of Science- Master of Science Clinical Research in Clinical Pharmacokinetics Assistant Fee

$92000

Tuition Fee

$NA

Average Cost of Living

$1300

Application Fee

Integrated Bachelor of Science- Master of Science Clinical Research in Clinical Pharmacokinetics Admissions Requirements

  • Minimum 50% Marks at Higher and Senior Secondary level (10th and 12th) with Physics, Chemistry, Biology/ Math’s and English as a Major Subject.
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Detailed Program and Facts

30

Application Processing Days

Full Time On Campus

Program Intensity

Under Graduate

Program Level

48

Duration

Study Visa

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.

In addition this program also offers Artificial Intelligence and Machine Learning (AIML) applications in Clinical Research to upgrade Medical and Health Science. Machine Learning Techniques like pre-trained deep learning models and convolutional neural networks (CNN) provides excellent opportunities for drug-development processes and makes clinical trial more intelligent.

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This program specialization encourages students to explore the key principles of pharmacokinetics (PK) including factors that affect the absorption, distribution, metabolism, excretion, and binding of drugs and integrate these principles into the process of monitoring, evaluating and adjusting dosing for patients. It provides students with the ability to interpret drug concentration measurements in the context of the therapeutic window, along with the derivation of dosage adjustments to maintain therapeutic concentrations. Upon completion of the course, the student will contribute at planning, design and analysis of clinical studies from pharmacokinetic and pharmacodynamic (PD) perspective. They will apply this information in the clinical drug development process. It will also provide hands on experience with pharmacokinetic data analysis, advanced PK/PD modeling research with emphasis on disease progression modeling and implementation of mechanism-based approaches.

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