Temporary vacancies for Quality Leadership roles can happen anywhere and anytime, but must never adversely affect daily operations of the quality assurance function and its manifold responsibilities and accountabilities, in order to sustain full GxP compliance at all times. We at RQM GxP Consulting help you bridge such temporary gaps successfully and sustainably, and tailored to your specific needs and requirements. This allows for a customized, yet resource conscious approach to maintain and continually improve your company’s compliance status.
Likewise, RQM experts can readily support your company in the role of an external qualified person (“Fachtechnisch verantwortliche Person”, FvP) or responsible person in the area of pharmacovigilance (PV). The availability of an FvP is one of the central prerequisites for obtaining a manufacturing and/or distribution license in Switzerland. The FvP directly oversees manufacturing operations, logistics and distribution, and ensures appropriate handling of medicinal products. The ultimate responsibility for product quality lies with the FvP, who ensures all product meets specifications, and is manufactured and distributed according to applicable GxP regulations. Sound technical knowledge and profound experience of the incumbent are vital for any company and its products. The same requirements apply for the responsible person in the area of PV. We at RQM offer our support as an external FvP or PV responsible person on a contract basis, providing expert resources tailored to your needs and set-up, and helping you build and maintain a robust quality system for your company.