Products Used in Early Phase IND Studies
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Website http://www.compliance4all.com/control/w_product/~product_id=501658LIVE?channel=ourglocal_Jan_2018_SE |
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Category Good Manufacturing Practises, gmp compliance courses, gmp good manufacturing practice trainings, 2018 Online Webinars, advanced trainings in USA
Deadline: January 18, 2018 | Date: January 19, 2018
Venue/Country: Online, U.S.A
Updated: 2017-11-29 15:28:41 (GMT+9)
Call For Papers - CFP
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 materialWhat to do at really early stagesWhat about special IND studies?What about preclinical studies?Who Will Benefit:Regulatory Affairs personnel who coordinate activities for the CMC sections of submissionsQA/QC personnel who need to plan work on early stage materialR & D personnel who will contribute data to CMC sectionsProject managers for product development studiesQuality systems auditorsConsultantsSpeaker 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 .Event Fee: One Dial-in One Attendee Price: US$150.00Contact Detail:Compliance4All DBA NetZealous,Phone: +1-800-447-9407Email: supportcompliance4All.com
Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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