Mr. Luiz Grasso has over 17 years of experience in the biopharmaceutical, pharmaceutical, chemical, and vegan medicine industries, with just over 4 years of his career at PharmEng. He is a Medical Device lead auditor specialized in Medical Device Single Audit Program (MDSAP), EU Regulations, ISO 13485, and ISO 9001. With a broad range of experience in areas such as Quality Control, Pharmacopeia Compliance, Process Manufacturing, Testing Methods, Technology Transfer, Validation, and more – Luiz is a seasoned specialist in presential and remote consulting needs.