Netzealous LLC DBA - Compliance4All, Online
2018-01-19
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
Event Fee: One Dial-in One Attendee Price: US$150.00
Contact Detail: Compliance4All DBA NetZealous, Phone: +1-800-447-9407 Email: support@compliance4All.com
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