Yechiel Goldman, Ph.D.
Scientific Writer, Consultant
For over 20 years, Dr. Goldman has been working as a regulatory affairs professional in the biotech/pharma sector in Israel. During this period, he has prepared a wide variety of CMC, preclinical, clinical and regulatory documentation for submission to the FDA, EMA and Israeli MoH. He has extensive hands-on experience supporting US/EU/IL product development in oncology, neurology, cellular therapeutics and regenerative medicine.