View all Part time Masters in Drug Development in Denmark 2019/2020
A master is a graduate degree that is meant to be completed after finishing a bachelor. Although they may take between one and three years of study, most master's programs may be completed in about two years.
The field of drug development gives students the opportunity to work with numerous industry and regulatory organizations. In addition, a foundation in medicinal nutrition, individualized healthcare, and pharmaceutical drug research and development may be established.
Denmark's higher education puts emphasis on a technical higher education through the university learning. Most of the Danish universities also offers quality international students culture due to its relaxed Scandinavian attitude.
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”...