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  • Anke Maaßen

    "The compliance to the IVD regulation (EU) 2017/746 is challenging – we can support you."

    Anke Maaßen

    In Vitro Diagnostics

  • Birger Kintzel

    "Regulatory Affairs services from early drug development to life-cycle management for mature products - that is what I am offering to my clients."

    Birger Kintzel

    Regulatory Affairs

  • Michael Zimmermann

    "Our competence are medical devices – we support you to meet the challenging European clinical and regulatory requirements for your medical devices."

    Michael Zimmermann

    MD Clinical Evaluations, MD Quality Management, MD Regulatory Affairs

  • Wolf-Stefan Richter

    "Generating clean and clinically relevant data from imaging needs a considered integration of the disciplines of drug development, diagnostics and clinical imaging."

    Wolf-Stefan Richter

    Clinical Development, R&D Strategies

  • Frank Zollmann

    "Integrated discovery and development approaches ensure rigorous optimization of therapeutic concepts and of the subsequent preclinical and clinical development program, reducing late stage attrition and maximizing the probability of success."

    Frank Zollmann

    Clinical Development, Preclinical Development, R&D Strategies