Alicia Luna

-Marketing authorization of medical devices IVD: Immunology, Hematology and Haemostasis for Europe, Asia and America. - Renewals and variations of the of existing registers. - Review and approval of technical documentation. - Knowledge of legislation applicable for each country.

- Editing and managing of new SOP’s or with critical modifications of procedures, researching, proposing and agreeing on the new procedure. - Update on already existing SOP’s. Creation and delivery of Training List. -Distribution of controlled copies of SOPs and management of PDF SOPs. -Personal training (course in GMP for new collaborators, new SOPS version).

- Responsible and coordinator of all activities in the Pharmacy. - Active dispensing -Order Management and purchasing decisions. -Compounding, Cosmetics, Orthopedics, Child line, Phytotherapy.

-Management of bibliographic and documentary resources of the Services. -Study of current European laws on drugs and Medical devices for hospital use -Classification of drugs and stock management. -Detection and notification of adverse reactions, incompatibilities and interactions -Compounding.