Part time Master Degrees in Drug Development 2020 in Europe
Master’s degrees are advanced academic programs that are available in many different study areas. Master programs can typically be completed in about two to three years. Depending on the school, they can even be earned online.
Certification in drug development is typically targeted toward students with a background in pharmacy, biosciences, pharmacology, or chemistry. A variety of topics make up the curriculum, including bio-therapeutics, target identification and validation, and screening platforms.
Master Degree Part time in Drug Development in Europe
Master of Medicines Regulatory Affairs is a continuing education programme targeted at professionals in the pharmaceutical industry. Admission requires a minimum of two y
Learn how to facilitate sound and transparent regulatory decision-making
Master of Medicines Regulatory Affairs is a continuing education programme targeted at professionals in the pharmaceutical industry. Admission requires a minimum of two years of relevant work experience.
Experts within regulatory affairs are essential for companies facing an increasingly complex approval process for bringing new products to market. As a Master of Medicines Regulatory Affairs, you can help secure your company a safe, coherent and successful regulatory process.
The scientific approach of this master’s programme enables you to argue for clinical relevance and scientific legitimacy to ensure a strong, reliable and quality-based storyline....
Master of Industrial Drug Development is designed to meet the need for managers to coordinate the many elements involved in order to accelerate the drug development proce
Understand the entire drug development process from molecule to market access
Master of Industrial Drug Development is designed to meet the need for managers to coordinate the many elements involved in order to accelerate the drug development process and smooth the transition of candidate drugs to market.
Drug development is a long, complex process requiring the interaction of numerous specialist fields. Skilful coordination of all the disciplines involved, from early target identification and validation through safety and efficacy testing to market launch, can streamline the approach to the production of new medicines.
“It is essential that employees in the pharmaceutical industry understand the whole drug development process in order to appreciate their colleagues’ perspectives and objectives, to collaborate optimally and to be capable of making the right project decisions – through MIND they acquire the necessary insights and skills”...