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Curriculum

MCRPD curriculum comprises 66 credits, including 8 compulsory courses and a capstone project.

Core Area I – Clinical Therapeutics

  • CRPD6001 Clinical Therapeutics I   (9 credits)

  • CRPD6002 Clinical Therapeutics II   (6 credits)

  • CRPD6003 Clinical Therapeutics III   (6 credits)

This subject area equips students with an understanding of the therapeutic aspects of diseases commonly investigated in clinical trials, prepares them to tackle challenges with confidence and expertise, fosters their decision-making in healthcare settings, and helps them succeed in clinical research projects and product development.

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Core Area II – Clinical Research Management

  • CRPD6004 Fundamentals of Clinical Research   (6 credits)

  • CRPD6005 Clinical Trial Essentials   (6 credits)

  • CRPD6006 Medicine in the Real World   (6 credits)

This subject area covers fundamental concepts and methods in clinical research and introduces the latest advancements in modern medical technology. By highlighting key aspects of clinical trials, from study design and regulatory approval to data management and quality assurance, students will develop the necessary knowledge and skills to navigate the complexities of clinical trial conduct and ensure the successful execution of research studies.

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Core Area III – Healthcare Product Development

  • CRPD6007 Product Development and Project Management   (6 credits)

  • CRPD6008 Product Commercialization and Marketing   (6 credits)

This subject area introduces cutting-edge clinical and medical product development, biomedical engineering technologies, project management fundamentals, and strategic product commercialization. It enables students to acquire the skills and expertise required to lead successful products in the healthcare industry.

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Capstone

  • CRPD6004 Capstone Project    (15 credits)

This subject area covers fundamental concepts and methods in clinical research and introduces the latest advancements in modern medical technology. By highlighting key aspects of clinical trials, from study design and regulatory approval to data management and quality assurance, students will develop the necessary knowledge and skills to navigate the complexities of clinical trial conduct and ensure the successful execution of research studies.

Programme Leaflet

MCRPD Programme Leaflet

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Capstone Experience

Full-time students will have the opportunities to work with organisations/ companies in clinical research, pharmaceuticals, and medical devices through our internship programme.

These activities may include site visits, talks by invited experts, and practical demonstrations that cover the full spectrum of clinical trail management.

The experiential learning components allow students to enrich their understanding of real-world settings, observe the comprehensive processes  involved in clinical research, inspire their capstone project.

The capstone experience, provide valuable practical experience to help students advance their careers or pursue further studies.

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