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Greenlight Guru Medical Device Blog

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Erica Loring

Erica Loring
Erica Loring is Medical Device Guru at Greenlight Guru who has 15 years of experience in medical device and IVD as a Senior Manager of Quality and Regulatory. She comes to Greenlight Guru from MasterControl where she implemented eQMS platforms for dozens of global enterprise biotech companies. She specializes in ISO 13485 QMS Systems and Regulatory support. Erica enjoys working with a wide range of companies, learning about the variety of products and helping those companies reach their goals with a robust Quality System!

Author's Posts

Developing Pediatric Medical Devices: An Innovative Approach - Featured Image

Developing Pediatric Medical Devices: An Innovative Approach

The design and development of pediatric medical devices continue to be a challenging field.
Medical Device Biocompatibility 101 - Featured Image

Medical Device Biocompatibility 101

Medical device biocompatibility can be confusing, challenging, even frustrating for device professio...
The Ultimate Internal Audit Checklist Every Medical Device Company Needs - Featured Image

The Ultimate Internal Audit Checklist Every Medical Device Company Needs

It was nothing more than a checklist that saved $175 million and 1,500 lives.

The Greenlight Guru Medical Device Blog

Providing you actionable tips, best practices and insights for better medical device quality, compliance and product development.

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