Pharmaceutical Technology and Medicines Control

Study mode:On campus Study type:Full-time Languages: English
Local:$ 11.1 k / Year(s) Foreign:$ 25.7 k / Year(s)  
601–800 place StudyQA ranking:13682 Duration:1 year

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The MSc in Pharmaceutical Technology and Medicines Control at the University of Bradford is a comprehensive postgraduate program designed to equip students with the advanced knowledge and practical skills necessary to excel in the pharmaceutical industry. This course provides an in-depth understanding of the principles and practices involved in the development, manufacturing, and regulation of medicines, ensuring graduates are well-prepared to meet the demands of this highly regulated sector. Throughout the programme, students will explore key areas such as pharmaceutical formulation, quality assurance, validation processes, and regulatory compliance, gaining both theoretical insights and practical experience. The curriculum integrates modern techniques in drug development, including formulation science, analytical methods, and manufacturing processes, aligned with current industry standards and guidelines. Special emphasis is placed on medicines control, covering aspects such as safety, efficacy, and post-marketing surveillance, enabling students to understand the full lifecycle of medicinal products. The course also offers opportunities for industry placements and project work, fostering real-world experience and professional networking. Students are encouraged to develop critical thinking, problem-solving skills, and a thorough understanding of Good Manufacturing Practice (GMP) and other regulatory frameworks essential for ensuring the quality and safety of medicines. The programme is suitable for recent science graduates, professionals already working in the pharmaceutical sector seeking to advance their careers, or individuals interested in entering this vital industry. Upon successful completion, graduates will possess the expertise to work in pharmaceutical manufacturing, quality assurance, regulatory affairs, or research and development. The University of Bradford’s state-of-the-art facilities, experienced faculty, and strong industry links provide an excellent environment for learning and professional growth. Join the MSc in Pharmaceutical Technology and Medicines Control to develop your expertise and contribute to the development of safe, effective, and innovative medicines that improve lives worldwide.

The programme structure is modular and the taught components run over two semesters (September to January then late-January to May), with the research project taking place between May and August.

All module information is for 2019 entry, and is subject to change. 

Please visit our website for a full list on course modules. 

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.

Fees for 2019 entry listed below.

Home/EU: £8,160 per year

International: £18,940 per year

The MSc Pharmaceutical Technology and Medicines Control at the University of Bradford is a comprehensive postgraduate programme designed to equip students with advanced knowledge and practical skills in the development, manufacturing, and regulation of pharmaceutical products. The course focuses on the science behind the formulation of medicines, quality assurance, and the regulatory frameworks that ensure medicines' safety and efficacy. Students will explore topics such as pharmaceutical formulation, drug delivery systems, quality control processes, and the legal and ethical considerations involved in medicines regulation.

The programme emphasizes a combination of theoretical learning and practical laboratory work, preparing graduates for careers in pharmaceutical industries, regulatory agencies, or further research roles. Core modules include Pharmaceutical Formulation and Product Development, Quality Control and Assurance, Medicines Regulation and Policy, and Good Manufacturing Practice (GMP). Students will also undertake a research project, allowing them to apply their knowledge to real-world challenges in pharmaceutical technology and regulation.

The course is suitable for science graduates seeking to expand their careers into pharmaceutical development and regulation, as well as professionals already working in the field who aim to update their knowledge base. The programme benefits from the university’s strong links with industry partners, providing networking opportunities and potential for placements. With a focus on innovation, compliance, and safety, graduates will be well-equipped to contribute to the development of new medicines and ensure existing medicines meet regulatory standards.

The academic staff involved in this programme are experts in pharmaceutical sciences, with backgrounds spanning formulation science, pharmacology, and regulatory affairs. Students will have access to state-of-the-art laboratories and industry-standard equipment for their research and projects. The programme also emphasizes critical thinking, problem-solving, and effective communication skills, all essential for successful careers in the highly regulated pharmaceutical sector. Upon completion, graduates will gain a recognized qualification enabling them to pursue roles such as pharmaceutical scientist, quality assurance manager, regulatory affairs specialist, or research scientist.

The MSc Pharmaceutical Technology and Medicines Control is typically completed over one year of full-time study or part-time options over two years. The programme is delivered through a combination of lectures, tutorials, case studies, and practical sessions, ensuring an engaging and comprehensive learning experience. Graduates will be well-prepared to contribute significantly to the development, production, and regulation of medicines, supporting public health and industry standards worldwide.

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