Adverse Event Management During Medical Device Clinical Studies 2017 is a seminar dedicated to adverse event reporting during medical device trials across Europe.
Adverse Event Management During Medical Device Clinical Studies 2017 covers topics such as:
- The industry, its drivers and the challenges and opportunities
- Key techniques of an MBA to apply to your work
- Develop your leadership skills
- What strategic thinking is and how to use strategy tools within BioPharma
- Coping wih and managing change in the Bio/Pharma Industry
- Gain confidence when making commercial decisions
- Different lifestyle management and marketing in the Bio/Pharma Industry
- The essentials of managing projects in the Bio/Pharma Industry
- The benefits and costs of doing an MBA
