View all Part time Masters in Pharmaceutical Medicine in Denmark 2019/2020
Pharmacy is an academic field focusing on human biology, anatomy, chemistry, pharmaceutics, and pharmacology. Pharmacists ensure the quality, supply, and type of medicines prescribed to patients are in order. They also advise patients about medicines.
Denmark, officially the Kingdom of Denmark, is a sovereign state in Northern Europe, located southwest of Sweden, south of Norway, and bordered to the south by Germany.
Part time Master Degree in Pharmaceutical Medicine in Denmark
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”...