San Francisco Events

Products Used in Early Phase IND Studies

Friday

Jan 19, 2018 – 10:00 AM - 11:30 AM

Online Event
San Francisco, CA 94103 Map

More Info

Overview:
How it may be integrated with the recommendations of the guidance

documents on CMC requirements.

Areas Covered in the Session:
Discussion of the elements found in the guidance document for Phase 1

material
What to do at really early stages
What about special IND studies?
What about preclinical studies?

Who Will Benefit:
Regulatory Affairs personnel who coordinate activities for the CMC

sections of submissions
QA/QC personnel who need to plan work on early stage material
R & D personnel who will contribute data to CMC sections
Project managers for product development studies
Quality systems auditors
Consultants

Speaker Profile:
Steven S. Kuwahara , Ph.D. is the founder and Principal of GXP

BioTechnology LLC, a consulting firm that works in the areas covered

by the GLP and GMP of drugs, biologics, and nutraceuticals. Steve has

over 30 years of experience in supervising quality control laboratories,

including an animal testing facility, and in performing GLP and GMP

audits of internal and external testing laboratories .

Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: support@compliance4All.com
One Dial-in One Attendee Price: US$150.00

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