Dr. Roberto Avila
Microbiologist from UCR with 10 years of experience in the industrial microbiology field. Broad experience in Quality Management Systems implementation based on ISO/IEC 17025 for laboratory, and applied experience in ISO 13485 working for medical devices manufacturing industry. Lead auditor for QMS based in ISO 17025.
Eng. Mauren Monge
Biotechnology Engineer from ITCR, with 11 years of experience in the medical devices industry field. Experience in microbiological quality assurance of medical device manufacturing and sterilization processes (ETO, gamma radiation and e-beam, dry heat). Knowledge in quality system requirements based on ISO 13485 and ISO 17025.