Gisah Bittencourt Sad
Regulatory Affairs professional with over 6 years’ experience in the medical device industry including implantable devices and IVD. Gisah holds a degree in Pharmacy, Biochemistry and Industrial Pharmacy and has Post Graduate Specialization in Project Management. Gisah has been a leader of medical devices submission processes within a number of different regulatory jurisdictions across U.S., European Union, Brazil and more recently in Australia. With a passion for continuous improvement, Gisah’s attention to detail has driven numerous successful medical device regulatory approvals.
- On 21/02/2019