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Stephen Scypinski,Ph.D.

David Guyer, M.D.



Edited by Stephen Scypinski, Ph.D. - Vice President, Analytical Development and Quality Control, Eyetech Pharmaceuticals.

Dr. Scypinski received his B.S., M.S. and Ph.D. degrees in Chemistry from Seton Hall University. Involved in analytical and pharmaceutical chemistry for over 22 years, Dr. Scypinski has held positions at Exxon Research and Engineering Co., Varian Instrument Group, Berlex Laboratories and Hoffmann-La Roche. His most recent position prior to joining Eyetech was Director of the Analytical Chemistry Research & Development Department at The R.W. Johnson Pharmaceutical Research Institute. An accomplished scientist as well as manager, Dr. Scypinski serves on the editorial review board for several analytical chemistry journals and is co-editor of the textbook “Handbook of Pharmaceutical Analysis.” Well-versed in both the scientific and regulatory facets of pharmaceutical analysis, Dr. Scypinski has experience both in US and worldwide regulatory filings as well as the pre-approval inspection process.


Co-authored by David Guyer, M.D., Chief Executive Officer, Eyetech Pharmaceuticals

Author of over 100 publications, Dr. Guyer is an internationally recognized authority on macular diseases, particularly the use of anti-angiogenic drugs for treating AMD and DME. His academic title is Professor and Chairman of the Ophthalmology Department at the New York University School of Medicine. Dr. Guyer was the Study Co-chairman of the Pharmacological Therapy for Macular Degeneration Study Group, a 45-center worldwide group of retinal specialists studying drug therapy for AMD. This Study Group performed the first Phase III study of a drug for AMD.

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