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Thomas Walton is listed as RA Consultant: Pharma and Medical Devices at CompassPointe South LLC: Regulatory and Quality Advisors, based in Sarasota, Florida, United States. AeroLeads shows a work email signal at msn.com and a matched LinkedIn profile for Thomas Walton.
Thomas Walton previously worked as Regulatory Affairs Specialist at Smith & Nephew and Manager, Regulatory Affairs, Biologics at Allergan. Thomas Walton holds B.S., Health Science from California State University, Long Beach.
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Thomas Walton is a RA Consultant: Pharma and Medical Devices at CompassPointe South LLC: Regulatory and Quality Advisors. He possess expertise in regulatory submissions, iso 13485, regulatory affairs, fda, medical devices and 12 more skills.
Listed skills include Regulatory Submissions, Iso 13485, Regulatory Affairs, Fda, and 13 others.
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Tampa/St. Petersburg, Florida Area
Currently assisting with IND submission for a dermatology start-up
Tampa/St. Petersburg, Florida Area
Regulatory Affairs Specialist for OTC Dermatology products and Class I and II Wound Care Medical Devices: US and CE markets
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Thomas Walton works for CompassPointe South LLC: Regulatory and Quality Advisors.
Thomas Walton is listed as RA Consultant: Pharma and Medical Devices at CompassPointe South LLC: Regulatory and Quality Advisors.
AeroLeads has found 1 work email signal at @msn.com for Thomas Walton at CompassPointe South LLC: Regulatory and Quality Advisors.
Thomas Walton is based in Sarasota, Florida, United States while working with CompassPointe South LLC: Regulatory and Quality Advisors.
Thomas Walton has worked for Compasspointe South Llc: Regulatory And Quality Advisors, Smith & Nephew, and Allergan.
You can use AeroLeads to view verified contact signals for Thomas Walton at CompassPointe South LLC: Regulatory and Quality Advisors, including work email, phone, and LinkedIn data when available.
Thomas Walton holds B.S., Health Science from California State University, Long Beach.
Thomas Walton is listed with skills including Regulatory Submissions, Iso 13485, Regulatory Affairs, Fda, Medical Devices, Pharmaceutical Industry, Dermatology, and Oncology.
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