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This profile was last updated on 4/6/2017 and contains contributions from the  Zoominfo Community.

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Wrong Jeffrey Roberts?

Jeffrey N. Roberts

Medical Officer

Food and Drug Administration

HQ Phone:  (301) 827-6500

Direct Phone: (301) ***-****direct phone

Email: j***@***.gov

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I agree to the Terms of Service and Privacy Policy. I understand that I will receive a subscription to ZoomInfo Community Edition at no charge in exchange for downloading and installing the ZoomInfo Contact Contributor utility which, among other features, involves sharing my business contacts as well as headers and signature blocks from emails that I receive.

Food and Drug Administration

5600 Fishers Lane

Rockville, Maryland,20852

United States

Company Description

China's Food and Drug Administration (SFDA) is now offering a reward of about 50,000 US dollars for relevant information on counterfeit drug production. The bounty aims to "encourage the public to report illegal activities so as to determine, control and elimi...more

Web References(14 Total References)


Medical Device Consultants Regulatory Services Staff - MDCI

www.mdci.com [cached]

Regulatory Services Staff | Regulatory Services Staff | Vicki Anastasi, Vice President of Regulatory Services and Business Development | Mary McNamara-Cullinane, RAC, Senior Regulatory Consultant | Cynthia J. M. Nolte, Ph.D., RAC, Senior Regulatory Consultant | Gail E. Radcliffe, Ph.D., Affiliate Principal Regulatory Consultant | Jeffrey B. Roberts, Regulatory Consultant | Rosina Robinson, RN, M.Ed., RAC, Principal Consultant | Mark W. Sheehan, Regulatory Associate | Cynthia A. Sinclair, RAC, Principal Consultant | Ronald S. Warren, RAC, CTBS (AATB), Principal Consultant | Randy Veale, Strategic Regulatory Advisor
Jeffrey B. Roberts, Regulatory Consultant Jeffrey B. Roberts, Regulatory Consultant Jeff has over twelve years experience in medical device regulatory affairs and quality management. He works closely with medical device manufacturers and suppliers to address FDA premarket requirements and ongoing quality assurance for a wide range of medical devices and systems. Prior to joining MDCI Jeff was Regulatory Affairs Manager at Candela Corporation, where he was responsible for the development, negotiation, and implementation of U.S. FDA and international regulatory strategies for Candela's medical and aesthetic laser devices with indications for tattoo removal, hair removal and acne scar treatment. At Confluent Surgical, he managed FDA, EU and other international submissions for class II and class III absorbable implant medical devices with abdominal and neurosurgical indications. Jeff also served as a Project Quality Engineer at Mitek Products / Johnson & Johnson, a leading orthopedic product developer and manufacturer, where he was involved in surgical sports medicine and soft tissue repair devices. Jeff holds his B.S. in Mechanical Engineering Technology from Wentworth Institute of Technology in Boston, MA. He is a member of the Regulatory Affairs Professionals Society and is a Regulatory Affairs Certification candidate.


Pregnancy Testing | Clinical Trials Transformation Initiative

www.ctti-clinicaltrials.org [cached]

Jeffrey Roberts (FDA)


News - MDCI Appoints New Regulatory Consultant - MDCI

www.mdci.com [cached]

MDCI Welcomes Jeff Roberts as Regulatory Consultant
Jeff Roberts will provide regulatory and clinical trial guidance to medical device clients Medical Device Consultants, Inc. (MDCI), a leading regulatory consulting firm and CRO for the medical device industry is pleased to welcome Jeffrey Roberts as Regulatory Consultant to its Massachusetts headquarters. "Every day we speak with new and existing clients who are developing novel, exciting and innovative medical technologies. In response the continuing need for experienced and knowledgeable regulatory affairs and quality assurance support, MDCI is please to welcome Jeff to our team, said Vicki Anastasi, Director of Regulatory Services. Jeff has over twelve years experience in medical device regulatory affairs and quality management. He works closely with medical device manufacturers and suppliers to address FDA premarket requirements and ongoing quality assurance for a wide range of medical devices and systems. Prior to joining MDCI Jeff was Regulatory Affairs Manager at Candela Corporation, where he was responsible for the development, negotiation, and implementation of U.S. FDA and international regulatory strategies for Candela's medical and aesthetic laser devices with indications for tattoo removal, hair removal and acne scar treatment. At Confluent Surgical, he managed FDA, EU and other international submissions for class II and class III absorbable implant medical devices with abdominal, cranial and spinal indications. Jeff also served as a Project Quality Engineer at Mitek Products / Johnson & Johnson, a leading developer and manufacturer of surgical sports medicine and soft tissue repair devices. Jeff holds his B.S. in Mechanical Engineering Technology from Wentworth Institute of Technology in Boston, MA. He is a certified Quality Engineer and is a Regulatory Affairs Certification candidate.


CAMI - Symposium Participants

www.cami-health.org [cached]

Jeff Roberts, MD
FDA/CBER


www.aptivsolutions.com

Jeffrey Roberts | Regulatory Consultant
Jeff has been with Aptiv Solutions since 2008, and brings FDA and international regulatory experience with aesthetic laser devices , as well as class II and class III absorbable implant medical devices with abdominal and neurosurgical indications.


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