Pharmaceutical Regulatory Sciences MS Postgraduate Programme By Temple University |TopUniversities
Subject Ranking

# 351-400QS Subject Rankings

Main Subject Area

Pharmacy and PharmacologyMain Subject Area

Programme overview

Main Subject

Pharmacy and Pharmacology

Degree

MSc

Study Level

Masters

Study Mode

On Campus

The Master of Science in Pharmaceutical Regulatory Sciences in the School of Pharmacy at Temple University addresses the immediate need for professionals well versed in regulatory science. The curriculum offers courses from pharmaceutical science and regulatory affairs (RA) and quality assurance (QA), bridging the gaps in knowledge that often exist between these areas. This master of science degree is part of the RA and QA graduate program.


What is regulatory science?


The Food and Drug Administration (FDA) defines regulatory science as the “science of developing new tools, standards and approaches to assess the safety, efficacy, quality and performance of FDA-related products.” Both regulated industry and regulatory agencies need professionals who understand the complex integration of regulations, quality practices and scientific knowledge required to bring regulated healthcare products to market. 


Pharmaceutical science courses focus on the core science principles involved in the development and manufacturing of therapeutic products. RA and QA courses provide a strong framework of regulations and quality practices, addressing scientific methods needed to assure safety, efficacy, quality and consistent performance. 


The curriculum draws upon the school’s world-renowned MS program in RA and QA. Courses are taught by pharmaceutical scientists actively engaged in research as well as industry experts currently working in research and development, drug development, regulatory affairs, manufacturing, and validation. 


Individuals pursuing this master’s in regulatory science graduate program must have strong science backgrounds, which include an undergraduate or graduate degree in the hard sciences. 


Regulatory Affairs and Quality Assurance at the School of Pharmacy 


The first university to develop a graduate program in quality assurance and regulatory affairs, Temple’s School of Pharmacy continues to set the gold standard in this dynamic professional discipline. Since 1968, the school has remained in the forefront of industry education, offering more courses in RA and QA than any other similar graduate program. Each year we continue to add and refine the curriculum to incorporate the latest trends in regulatory sciences.  


RA and QA courses expose students to real-world developments in the pharmaceutical industry, from current quality practices to the latest trends in domestic and global regulation. Throughout their course of study, RA and QA students gain a greater appreciation for benefit-risk assessment, regulatory intelligence, data mining and statistical relevance, and the complexities of blending pharmaceutical and regulatory science on a global scale.  


Careers and Networking


Most students work in industry, representing the world’s foremost pharmaceutical, device and biotechnology companies. Their experience and knowledge vary considerably: Some are just starting their careers, while others have been involved in industry for thirty years or more.   


With students and faculty drawn from more than 300 companies, the networking opportunities are tremendous. Each classroom experience coalesces the experiences of individuals from multiple aspects of the industry, including quality assurance and control, regulatory science, R&D, manufacturing and validation, clinical research and trials, medical affairs and pharmacovigilance, biotechnology and generic drugs, medical devices and combination products, and marketing and sales.   


Students from the cosmetic, chemical, healthcare and food industries also participate to gain a deeper understanding of quality practices and regulatory compliance.

Programme overview

Main Subject

Pharmacy and Pharmacology

Degree

MSc

Study Level

Masters

Study Mode

On Campus

The Master of Science in Pharmaceutical Regulatory Sciences in the School of Pharmacy at Temple University addresses the immediate need for professionals well versed in regulatory science. The curriculum offers courses from pharmaceutical science and regulatory affairs (RA) and quality assurance (QA), bridging the gaps in knowledge that often exist between these areas. This master of science degree is part of the RA and QA graduate program.


What is regulatory science?


The Food and Drug Administration (FDA) defines regulatory science as the “science of developing new tools, standards and approaches to assess the safety, efficacy, quality and performance of FDA-related products.” Both regulated industry and regulatory agencies need professionals who understand the complex integration of regulations, quality practices and scientific knowledge required to bring regulated healthcare products to market. 


Pharmaceutical science courses focus on the core science principles involved in the development and manufacturing of therapeutic products. RA and QA courses provide a strong framework of regulations and quality practices, addressing scientific methods needed to assure safety, efficacy, quality and consistent performance. 


The curriculum draws upon the school’s world-renowned MS program in RA and QA. Courses are taught by pharmaceutical scientists actively engaged in research as well as industry experts currently working in research and development, drug development, regulatory affairs, manufacturing, and validation. 


Individuals pursuing this master’s in regulatory science graduate program must have strong science backgrounds, which include an undergraduate or graduate degree in the hard sciences. 


Regulatory Affairs and Quality Assurance at the School of Pharmacy 


The first university to develop a graduate program in quality assurance and regulatory affairs, Temple’s School of Pharmacy continues to set the gold standard in this dynamic professional discipline. Since 1968, the school has remained in the forefront of industry education, offering more courses in RA and QA than any other similar graduate program. Each year we continue to add and refine the curriculum to incorporate the latest trends in regulatory sciences.  


RA and QA courses expose students to real-world developments in the pharmaceutical industry, from current quality practices to the latest trends in domestic and global regulation. Throughout their course of study, RA and QA students gain a greater appreciation for benefit-risk assessment, regulatory intelligence, data mining and statistical relevance, and the complexities of blending pharmaceutical and regulatory science on a global scale.  


Careers and Networking


Most students work in industry, representing the world’s foremost pharmaceutical, device and biotechnology companies. Their experience and knowledge vary considerably: Some are just starting their careers, while others have been involved in industry for thirty years or more.   


With students and faculty drawn from more than 300 companies, the networking opportunities are tremendous. Each classroom experience coalesces the experiences of individuals from multiple aspects of the industry, including quality assurance and control, regulatory science, R&D, manufacturing and validation, clinical research and trials, medical affairs and pharmacovigilance, biotechnology and generic drugs, medical devices and combination products, and marketing and sales.   


Students from the cosmetic, chemical, healthcare and food industries also participate to gain a deeper understanding of quality practices and regulatory compliance.

Admission Requirements

58+
3+
7+
85+
Bachelor's Degree in Discipline/Related Discipline: A baccalaureate degree in Pharmacy, Biochemistry, Biology, Chemistry, Chemical Engineering or Mechanical Engineering is required.

Jan
Jun

  • Candidates are required to submit references or letter(s) of recommendation for acceptance

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