Wayland Rushing
Biochemistry and Molecular Genetics, Pharmacy and Medicine
Columbia, Missouri, United States of America
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Dr. Wayland Rushing is a technical expert in Chemistry Manufacturing and Controls (CMC) program design, analytical development and regulatory submissions. Over his career, he has led CMC development programs for a wide array of pharmaceutical products, including parenterals, inhalation drugs, drug/device combinations and other therapies with complex delivery systems.
Dr. Rushing is a subject matter expert in HPLC and GC method development and validation, extractables and leachables program design and regulatory submission requirements; has drafted multiple IND and NDA submissions; and assists ABC clients in responding to FDA deficiency letters. Dr. Rushing currently serves on Parenteral Drug Association (PDA) advisory committees for Technology Transfer and Elastomeric Closures and Seals Defects.
Dr. Rushing is a subject matter expert in HPLC and GC method development and validation, extractables and leachables program design and regulatory submission requirements; has drafted multiple IND and NDA submissions; and assists ABC clients in responding to FDA deficiency letters. Dr. Rushing currently serves on Parenteral Drug Association (PDA) advisory committees for Technology Transfer and Elastomeric Closures and Seals Defects.
EVENTS & ACTIVITIES (Speaking, Spoken, and Authored)
6th Annual Venous Symposium New York
In-Person Event
Vascular Disease ...
Apr 16 - 18, 2015
New York, New York, USA
10th Annual Conference on Stability Program for Pharmaceutical and Biopharmaceutical Manufacturers 2014
- In-Person Event
- Pharmacy and Medicine
- May 14 - 15, 2014
- Somerset, New Jersey, USA
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