Medwork is ideally situated in a geographical area with an increasing need for pharmaceutical quality services. Clinical trials and pharmacovigilance systems in Southeast Europe and the Middle East are required to be audited against the same quality standards as those in Northwest Europe. Cooperation with a reliable regional partner can contribute to reducing travel and frustration for your staff as well as lowering expenses for your organization.

Medwork can assist you with
  • Building a corporate quality-oriented mind-set

    by improving your personnel's understanding of quality requirements at all levels and functions throughout your organization

  • Integrating quality into your daily working environment

    and processes while maintaining flexibility appropriate to the size, needs and particularities of your organisation

  • Ensuring compliance and minimising regulatory risk

    by improving your responsiveness to a demanding and fast-changing environment

  • GVP audits/ inspections preparation and follow-up.