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.
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.