Chemistry, Manufacturing, and Controls (CMC) outsourcing/ Contract Development and Manufacturing Organization (CDMO) management

Meet a panel of experts Chemistry, Manufacturing, and Controls (CMC) outsourcing/ Contract Development and Manufacturing Organization (CDMO) management.

Speakers



Sukhon Likitlersuang

is currently leading a CMC & Technical Operation
department including formulation/process
development/technical operation and
analytical/QC team. Extensive experience in
evaluating potential and managing outsourcing
vendors including consultants, CDMOs, CTO, and
CPOs etc. to align with company business clinical
and commercial launch strategies.

YiBin Lin

is the associate director of analytical development
in Landos Biopharma and is a certified
pharmaceutical GMP professional (CPGP), quality
engineer (CQE), quality manager and organization
excellence (CQM/OE), and US regulatory affairs
professional (RAC). Yibin has more than 10 years
of working experience managing CRO and CDMO
worldwide.

Dana Copenhaver

has over 15 years’ experience in CMC drug
substance development in the pharmaceutical
industry. She has broad regulatory CMC
experience focusing on phase appropriate and fit
for intended purpose regulatory strategies. She is
currently Principal Consultant at Cope Pharma
Consulting, LLC. Cope Pharma Consulting provides
quality strategies and technical solutions for
successful drug development.

When

9 March 2024 (Saturday)

5:00-7:00 PM (PST) onsite

5:00-7:00 PM (PST) Zoom

Where

Zoom meeting and

Irvine water district conference room, 15600 Sand Canyon Ave, Irvine, CA 92618

Free Registration

registration link for onsite
registration link for Zoom

Questions

Website: http://www.sabpa-ocla.org

Email: Sabpa.ocla@gmail.com