MASTER OF INDUSTRIAL DRUG DEVELOPMENT Get insight into the entire drug development process from molecule to market access Developed in close collaboration between University of Copenhagen and the pharmaceutical industry Courses combine outstanding academic-based research with an extensive contribution from leading experts from the pharmaceutical industry Enroll in the full programme or take individual courses Courses in 2017/2018 Biopharmaceuticals Drug Development Quality by Design (QbD) in Pharmaceutical Development Market Access for Pharmaceutical Products – trends and challenges QA, QC, GXP for Pharmaceutical Production Clinical Pharmacology and Biostatistics Discovery and Development of Medicines Drug Discovery Non-Clinical Safety and Toxicology Read more at mind.ku.dk or e-mail master@sund.ku.dk MASTER OF MEDICINES REGULATORY AFFAIRS Become the expert that can help secure a safe, coherent and successful regulatory process The Master will give you Thorough insight into the regulatory process at all stages during the development of medicines An overview of the differences in regulatory demands globally The competencies to analyse, predict and advise on medicines regulations and directives The Master programme is offered in collaboration with Medicademy – part of Lif Education. Enroll in the full programme or take individual courses Courses in 2017/2018 Regulatory Science – Perspectives on Clinical Development Global Medicines Legislation and Guidelines Regulatory Affairs in the EU Ethics in Regulatory Affairs of Pharmaceutical Products – Dilemmas in Decision-makings Safety of Medicines – From Non-clinical Development to Pharmacovigilance Quality – Active Substance and Medicinal Product Biopharmaceuticals – Quality Development and Documentation Clinical Development – Efficacy of Medicines Regulatory Affairs in the USA Read more at mra.ku.dk or e-mail master@sund.ku.dk
Download PDF fil
Se arkivet med udgivelser af Dansk Kemi her
TechMedias mange andre fagblade kan læses her