Luiz is based in Barcelona, Spain, and has over 17 years of experience in the biopharmaceutical, pharmaceutical, chemical, and Vegan medicine industries. He is a Medical Device lead auditor, specialized in Medical Device Single Audit Program (MDSAP), Regulations (EU) 2017/745 & (EU) 2017/746, ISO 13485, and ISO 9001. He has a broad range of experience in areas such as Quality Control, Quality Assurance, Pharmacopeia Compliance, Process Manufacturing, Testing Methods, Technology Transfer, Stability Studies, Project Leadership and Validation. Mr. Grasso is a specialist in PRESENTIAL and REMOTE consulting needs, MDSAP & European directives full AUDIT compliance.
Luiz Grasso
