Kim Huynh-Ba
PHARMALYTIK C.S.
32 Forest Ridge
Newark, DE 19711
Phone:
(302) 731-9959
Fax:
(302) 598-4297
E-mail: kim.huynhba@pharmalytik.com
Web Page: www.pharmalytik.com
Specialties:
- Pharmaceutical
- Quality
- Technology Transfer
- Analytical
- Project Management
- Outsourcing
- Expert Witness
Services:
Kim Huynh-Ba has over 24 years of experience in various analytical areas of pharmaceutical development and a primary focus in stability sciences. She specializes in analytical development, stability, outsourcing and technology transfer management. She has been involved with several projects harmonizing and optimizing analytical best practices in several companies, including those under Consent Decree.
Prior to Pharmalytik, she worked at Astra Zeneca, DuPont Pharmaceuticals, Bristol Myers Squibb and Wyeth Vaccines.
Kim has authored numerous technical publications and is invited frequently to present at national and international conferences. She is the editor of the "Handbook of Stability Testing in Pharmaceutical Development: Regulations, Methodologies and Best Practices" (published Nov. 2008), and also "Current Trends of Stability Testing to Support Global Markets" (expected 2009).
Since 2001, she has conducted training activities on cGMP compliance and quality issues for global organizations such as ACS, AAPS, Pittsburgh Conference, IIR, SWE, IVT, CBI and Benastrum. She is the founder and past-chair of the AAPS Stability Focus Group, and served on the Steering Committee of the CMC Focus Group. She is an active member of AAPS, PSDG, as well as serving on the Governing Board of Eastern Analytical Symposium (EAS). She currently is Chair of the EAS Short Course Program and the AAPS APQ Distance Learning Committee. She is a member of USP's P/NP stakeholder's forum and also USP Reference Standard Project Team.
Kim is a recipient of the 2008 APQ Service Award and 2008 Recognition Award of AAPS Regulatory Section. She also received the 2001 DPCAA Leadership Award.
