Dr Roberto Liddi

Vice President Regulatory & Compliance at NuraLogix Corporation
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Contact Information
us****@****om
(386) 825-5501
Location
Oxford, England, United Kingdom, UK
Languages
  • English Native or bilingual proficiency
  • Italian Native or bilingual proficiency
  • Spanish Professional working proficiency
Skills

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Jason Richards

I had the pleasure of working with Roberto Liddi during my time at Sword Health and I highly recommend him for any leadership role in the medical device manufacturing industry. Roberto possesses a breadth of knowledge around compliance and regulatory affairs that is truly impressive. He is a results-oriented leader with a strong executive presence and excellent people skills. Roberto's ability to manage complex projects and drive organizational change is truly outstanding. He is a true professional and an asset to any team.

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Credentials

  • MTOPRA
    TOPRA

Experience

  • NuraLogix Corporation
    • Canada
    • Wellness and Fitness Services
    • 1 - 100 Employee
    • Vice President Regulatory & Compliance
      • Jun 2023 - Present

  • Sword Health
    • United States
    • Wellness and Fitness Services
    • 500 - 600 Employee
    • Vice President
      • May 2022 - Jun 2023

      Global Quality and Regulatory strategies Global Quality and Regulatory strategies

  • Sensyne Health
    • United Kingdom
    • Biotechnology Research
    • 1 - 100 Employee
    • Chief Regulatory Quality & IG Officer
      • May 2021 - May 2022

    • Senior Vice President Quality Regulatory & IG
      • Dec 2019 - Apr 2021

    • Vice President Quality and Regulatory
      • 2018 - Dec 2019

  • STS Medical Group
    • Medical Equipment Manufacturing
    • 1 - 100 Employee
    • Corporate Director QARA
      • Jan 2018 - May 2018

  • Renishaw plc
    • UK
    • Head of Corporate QARA Medical Divisions
      • May 2013 - Dec 2017

      Neurosurgical devices - Dental - Diagnostics Neurosurgical devices - Dental - Diagnostics

  • KCI Europe Holdings
    • Senior Director Regulatory Affairs and Regulatory Compliance EMEA
      • Apr 2009 - May 2013

  • KCI
    • Senior Director Regulatory Affairs and Regulatory Compliance EMEA
      • Apr 2009 - May 2013

  • Zimmer Biomet
    • United States
    • Medical Equipment Manufacturing
    • 700 & Above Employee
    • Associate Director
      • Apr 2007 - Mar 2009

  • Cozart plc
    • Biotechnology Research
    • 1 - 100 Employee
    • Head of QA
      • Mar 2001 - Aug 2005

      Manufacturer of on-site drug testing equipment using alternative biological matrix Manufacturer of on-site drug testing equipment using alternative biological matrix

  • UCLH, Middlesex Hospital
    • Lecturer
      • Mar 2000 - Mar 2001

      Research in diabetic nephropaties Research in diabetic nephropaties

Education

  • Università degli Studi di Bari
    Doctor in Biological Sciences, Human Biology
    1986 - 1991
  • Politecnico di Bari
    Master's degree, Immunology
    1991 - 1993
  • Di Cagno Abbrescia Bari

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