At first sight, utilizing biologically active macromolecules as drugs appears to be fairly straightforward since the biology of endogenous compounds such as peptides and proteins is something of a given (e.g. hormones, coagulation factors). Further, due to the recent tremendous advances in our genetic understanding and increased knowledge of protein functions in the biology of diseases, there has been a dramatic increase in the number of new opportunities for novel and improved biopharmaceuticals. In addition, new insight into formulation design and delivery approaches is continuously emerging. However, the complexity of pharmaceutical formulation design, development and safety assessment still poses huge challenges in the overall development of novel biopharmaceuticals.
This course provides you with an overview of the stages in the drug development process and highlights aspects of crucial importance for our ability to develop biologically active macromolecules. To further understand these aspects, the course has invited several leading experts in the field as guest lecturers. The course’s case-based approach will also introduce you to some of the latest advances in the development of effective biopharmaceuticals.
What you will learn:
- Understand and address major issues in the development of biopharmaceuticals including pharmaceutical formulation development, safety and efficacy testing
- Identify key challenges and suggest solutions for addressing critical issues in the development and testing of biopharmaceuticals
- Design and develop novel interdisciplinary approaches, thereby improving current practice in the development of biopharmaceuticals
- Communicate field-specific issues and solutions in the development of biopharmaceuticals to other specialists and project stakeholders
- Cooperate within a multi-disciplinary development project team
The course will address and highlight characteristics and procedures of relevance for the design and development of biopharmaceuticals. Experts from relevant fields will lecture on and discuss both fundamental concepts and specific selected issues related to biopharmaceutical drug development. Key topics requiring special attention will be selected from the discovery phase through development and assessment, and will include: Peptide and protein engineering, pharmaceutical drug design and formulation, experimental models, efficacy and safety assessment, and regulatory aspects. Case studies will form the basis for discussion sessions.
The University of Copenhagen has preapproved the course as an elective in the Master of Industrial Drug Development (MIND) programme and the Master of Medicines Regulatory Affairs (MRA) programme.
The course is for professionals in the pharmaceutical industry who need an interdisciplinary overview of the specific requirements for the development of biopharmaceuticals.
- Hold a relevant bachelor degree or equivalent
- Have a minimum 2 years of relevant job experience in drug development
- Be proficient at English
Registration deadline is 31 May, 2018
Read more about the course and register HERE