Automation Infrastructure GMP Industry 4.0
on 10/24/2019 at 14 pm
Meet the key challenges of meeting Good Manufacturing Practices within the automated environment.
- Regulatory Bases
- Automation environments (what are they?)
- Future Systems – Industry 4.0
- How to meet the minimum requirements
Graduated in Electrical and Mechatronics Engineering, and an MBA from FGV. He has 20 years of experience in automation projects in pharmaceutical and biotechnology industries. Specialized in development of automation projects for GAMP, CFR21Part11 and Validation oriented BPx environments. Has developed automation systems for process control, filling machines, inspection, washing and sterilization, CIP / SIP, packaging, BMS, FMS, MES, SCADA, in projects of Novo Nordisk, Libbs, Bionovis, Orygen, Fresenius, Biochimico, Butantan. During last years, leading the digital transformation in the pharmaceutical industry. Participated on the elaboration of Data Integrity – Manufacturing Records RDI Good Practice Guide from ISPE. He is the GAMP Brazil Committee Leader and member of the ISPE SIG Pharma 4.0