THE QUALITY AND EQUIVALENCE OF TOPICAL
PRODUCTS AND CHALLENGES Of NANOTECHNOLOGY
Specialized in the field of preclinical studies Labhnn is organizing its first hybrid workshop with the contribution of four international experts
See you in Geneva on April 06 2021
Workshop
EMA’s proposed guideline on quality and equivalence of topical products - future advances and challenges
On 6 April 2021
SPEAKERs
PROF. YOGESHVAR KALIA
Professor Kalia has worked in biopharmaceutics (speciality: transdermal drug delivery), first at the University of California – San Francisco since 1994
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PROF. RICHARD GUY
Richard Guy received an M.A. in Chemistry from Oxford University, and his Ph.D. in Pharmaceutical Chemistry from the UCL School of Pharmacy.
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DR. VINOD SHAH
Dr. Shah is a Pharmaceutical Consultant. He worked at US Food and Drug Administration (FDA) for over 30 years and developed several Regulatory Guidances
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PROF. STEFAN MUHLEBACH
Professor Mühlebach is a trained hospital pharmacist and pharmacologist. He worked for 25 years as head pharmacy in the hospital of Biel/Bienne
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Dr. Maria Lapteva
Dr. Maria Lapteva is currently occupying senior scientist in Prof. Kalia’s group. She has over 10 years of experience in preclinical drug development
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PROF. Christian Surber
Christian Surber, Ph.D., is Professor of Dermatopharmacology and Hospital Pharmacy at the University of Basel and visiting Professor at the Departments of Dermatology
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VENUE
For your venue we propose to book a room at Hotel Le Cenacle at 17, promenade Charles-Martin, 1208 Geneva .
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Challenges of new nanotechnology medical products
I’m Stefan Mühlebach, Prof. em. in Pharmacology and Hospital Pharmacy at the University of Basel in Switzerland. Due to my activity in nanopharmaceutical and regulatory science, I was a founding member of the Non-Biological Complex Drugs working party in the Netherland more the 10 years ago.
Quality and equivalence of topical products
My name is Richard Guy. I am Professor of Pharmaceutical Science at the University of Bath in the UK. Since 2013, my research has been funded by the FDA’s Office of Generic Drugs to develop and validate methods to assess the bioequivalence of topical drug products.
February 2021 -Teaser of Dr Vinod Shah – 30 years at the FDA
Dr. Vinod Shah, one of the hybrid workshop speakers about the Quality and Equivalence of Topical Products and Nanotechnology Challenges, is introducing his talk. This event will be held on 6 April 2021 in Geneva.
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