Our Team

Mr. Cligrow joined Biologics Consulting in June 2021 and has experience working in the drug/medical device industry, including a year working as an electronic publishing specialist. He worked with publishing tools to submit electronic submissions to the FDA via cloud software. Mr. Cligrow also has experience working in a laboratory setting including working in a parasitology lab to examine mammalian samples to determine the existence of parasites or other harmful bacteria.

Nolan previously worked for Hikma Pharmaceuticals as a regulatory affairs publishing specialist to submit original ANDA and NDA applications for approval to the FDA. In addition to original applications, submissions such as annual reports, PADERS, labeling, CBE-0 and CBE-30, as well as amendments were processed and compiled before sending to the FDA.

Prior to Hikma, he worked for IDEXX laboratories as an assistant lab technician in order to analyze and process samples from veterinarian clinics for the existence of parasites and harmful bacteria.

Mr. Cligrow has experience in reviewing eCTD-formatted applications as well as electronic publishing requirements and can compile various types of applications to be sent to the FDA for approval.

Education
Mr. Cligrow received his B.S. in Biochemistry from The Ohio State university in 2017 and obtained his M.S. degree in Bioinformatics from Jonhs Hopkins in 2019 where he studied genomic databases and how to process and parse them using various software and command-line tools such as Python, Java, and SQL.