Susan Mcloughlin's Location
Kingston upon Hull, England, GB
Susan Mcloughlin's Work
- Director of Regulatory Affairs @ Medtrade Products Limited
- MDR Clinical Safety and Medical Affairs PMO Lead @ Smith+Nephew
- Director of Regulatory Affairs @ Smith+Nephew
- Regulatory Affairs Manager @ Smith+Nephew
- Principal RA Officer - New Product Development @ Smith+Nephew
- Senior Regulatory Affairs Specialist @ Smith+Nephew
Susan Mcloughlin's Education
- University of Lincolnshire & Humberside1995 - 1998
- Wolfeton, Willerby/Kirkella, East Riding of Yorkshire
Susan Mcloughlin's Skills
- FDA
- Medical Devices
- Regulatory Affairs
- ISO 13485
- Regulatory Submissions
- Regulatory Requirements
- CE marking
- Quality System
- Sop
- Change Control
Susan Mcloughlin's Summary
Susan McLoughlin, based in Kingston upon Hull, England, GB, is currently a Director of Regulatory Affairs at Medtrade Products Limited, bringing experience from previous roles at Smith & Nephew. Susan McLoughlin holds a 1995 - 1998 University of Lincolnshire & Humberside. With a robust skill set that includes FDA, Medical Devices, Regulatory Affairs, ISO 13485, Regulatory Submissions and more, Susan McLoughlin contributes valuable insights to the industry. Susan McLoughlin has 1 email on RocketReach.
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