Parviz Bayegi

About the Author

Parviz Bayegi is a distinguished expert in pharmaceutical engineering and cleanroom design, with over two decades of experience in the biotechnology and medical device industries. Holding advanced degrees in chemical engineering and regulatory compliance, he has consulted for leading global firms, ensuring adherence to stringent GMP, FDA, and PIC/S standards. Bayegi's practical insights stem from hands-on projects in pharmacy, biotech, ATMP, and medical device manufacturing, where he has optimized cleanroom layouts to enhance efficiency and safety. His writing demystifies complex regulatory landscapes, offering actionable strategies for professionals navigating evolving guidelines like the EU-GMP Annex 1-2022. Through his publications, Bayegi empowers engineers and compliance officers to build robust, future-proof facilities that meet international benchmarks.