Robert Bronsing

Robert Bronsing Email and Phone Number

Leadership in Regulatory Strategy and People Management @ Esperante Development
Robert Bronsing's Location
Almere, Flevoland, Netherlands, Netherlands
Robert Bronsing's Contact Details

Robert Bronsing work email

Robert Bronsing personal email

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About Robert Bronsing

Regulatory Affairs professional with almost 20 years of experience in regulatory affairs. My focus is on leading teams to devise innovative and creative regulatory strategies to support patient centric drug development. With the teams, I help devise and refine preclinical and clinical study strategies to ensure the best possible outcomes for patients.

Robert Bronsing's Current Company Details
Esperante Development

Esperante Development

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Leadership in Regulatory Strategy and People Management
Robert Bronsing Work Experience Details
  • Esperante Development
    Director Regulatory Affairs And Member Of The Management Team
    Esperante Development Sep 2023 - Present
    Baarn, Utrecht, Nederland
    Director Regulatory Affairs leading a group of regulatory professionals and member of the Management Team of the organization, Esperante Development. Development of innovative regulatory strategies to help deliver value and trust to patients and development of the team to help deliver trust and value to the team members and organization.
  • Esperante Development
    Director Quality Assurance (Ad Interim)
    Esperante Development Jun 2024 - Oct 2024
    Baarn, Utrecht, Nederland
    Ad interim head of the quality assurance department for Esperante Development. Leading the department and ensuring business continuity and adherence to all quality standards.
  • Sanofi
    Regulatory Strategist @ Sanofi Global Regulatory Affairs
    Sanofi Jul 2023 - Sep 2023
    Amsterdam, Noord-Holland, Nederland
    Regulatory Strategist for innovative drug development in rare diseases. Input into pre-clinical and clinical development plans to help shape the overall development and enhance the probability of success and reduce regulatory risks.
  • Sanofi Genzyme
    Global Regulatory Lead - Rare Diseases And Rare Blood Disorders
    Sanofi Genzyme Jan 2022 - Sep 2023
    Amsterdam, North Holland, Netherlands
    Global Regulatory Team Leader for rare diseases and rare blood disorders. Take the lead in the Global Regulatory development of innovative drugs for several rare diseases, such as Alport, Achondroplasia and Osteogenesis Imperfecta. Ensure Global alignment on strategy in early and late phase development as well as alignment with company goals.
  • Sanofi Genzyme
    Global Regulatory Lead Neurology (Ad Interim)
    Sanofi Genzyme Apr 2021 - Dec 2021
    Amsterdam, Noord-Holland, Nederland
    As an acting Global Regulatory Lead in Neurology, i am responsible for the life cycle management of multiple sclerosis drugs and I am heavily involved in the early development stages of an investigational compound in ALS and MS. Translating global requirements and expectations to concrete recommendations for strategies in early clinical development. Devise strategies and tactics for important post approval studies, risk mitigation and harmonization of regulatory relevant documents. Close cooperation with regional and local regulatory experts, clinical and non-clinical scientists, risk management experts, CMC experts and other functions as needed.
  • Bronsing Life Science Consultancy
    Regulatory Affairs Strategist And Owner
    Bronsing Life Science Consultancy Feb 2020 - Dec 2021
    Almere Stad Area, Netherlands
    Helping companies to navigate the complex Regulatory landscape in Europe. Expertise in life cycle maintenance and development of new compounds for the European common market.
  • Bayer Healthcare Pharmaceuticals
    European Regulatory Affairs Manager
    Bayer Healthcare Pharmaceuticals Mar 2008 - Feb 2020
    Mijdrecht
    In this role I have devised and implemented the European Regulatory Strategy as a member of the Global Regulatory Team. I have obtained marketing approval for several products and have worked on the development strategy for many others. Focus on giving Europe a voice within the development team.
  • Ratiopharm
    Registration Officer
    Ratiopharm Mar 2007 - Feb 2008
    My main areas are legal affairs (license and supply agreements, import licenses, marketing authorisations, etc), project coördination (new launches, switches), medical information.
  • Eurocept
    Manager Pharmaceutical Affairs
    Eurocept Jan 2006 - Jan 2007
    End-responsibility for all pharmaceutical matters, quality assurance, pharmacovigilance, legal affairs.
  • Medicines Evaluation Board
    Registratie Coördinator
    Medicines Evaluation Board Apr 2004 - Dec 2005
    Regulatory affairs management, mainly european.
  • Erasmus Universiteit Rotterdam
    Ph.D. Student
    Erasmus Universiteit Rotterdam 1999 - 2004
  • Lerner Medical Technology
    Researcher
    Lerner Medical Technology 1998 - 1999

Robert Bronsing Skills

Regulatory Affairs European Union Pharmaceutics Pharmaceutical Industry Regulatory Submissions Lifesciences Biotechnology Oncology R&d Quality Assurance Licensing Biopharmaceuticals Regulatory Requirements Drug Development Life Sciences

Robert Bronsing Education Details

Frequently Asked Questions about Robert Bronsing

What company does Robert Bronsing work for?

Robert Bronsing works for Esperante Development

What is Robert Bronsing's role at the current company?

Robert Bronsing's current role is Leadership in Regulatory Strategy and People Management.

What is Robert Bronsing's email address?

Robert Bronsing's email address is ro****@****yer.com

What schools did Robert Bronsing attend?

Robert Bronsing attended Universiteit Leiden, Era Cursus, Willem De Zwijger College, Fontein Mavo.

What skills is Robert Bronsing known for?

Robert Bronsing has skills like Regulatory Affairs, European Union, Pharmaceutics, Pharmaceutical Industry, Regulatory Submissions, Lifesciences, Biotechnology, Oncology, R&d, Quality Assurance, Licensing, Biopharmaceuticals.

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