valerio duranti

High-level Training in Clinical Research ( 40h ); - Methodology and normative of clinical trial; - Good Clinical Practice (GCP); - Good Manufacturing Practices (GMP); - Pharmacovigilance; - Quality systems and quality assurance; - Monitor tasks referred to in paragraph 5.18 of Annex 1 to the Ministerial Decree of 15 July 1997 - Ensure that the laboratories comply with the cleaning and safety standards; - Develop and qualify new verification methods; - Work in staff with other analysts to perform laboratory and test procedures; - Perform visual inspections of finished products; and more over