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GlobalCompliancePanel, USA
2010-11-16
These guidelines remove some of the problems that are encountered with early phase products and are in addition to those that cover the CMC sections for IND submissions at Phase 1. Although the guidance appears to remove the need to follow GMPs for Phase 1 products, the need to follow GMPs is still present in the Food, Drug, and Cosmetic Act. Thus the nature and extent of GMP-related activities will depend upon the nature of the investigational drug and the extent of the study that is planned. This presentation will review the GMP guidance document and discuss 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?
- Varying GMP activities that depend upon the nature of the IND product.
- What are the requirements for the GMP found in the Food, Drug, and Cosmetic Act?
- What to do about QC activities such as instrument qualification, method validation, and process validation.
Who Will Benefit: This presentation will be aimed at helping Regulatory, Quality Assurance and Quality Control personnel to understand the varying types of GMP activities that accompany early stages of Product development. - 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
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Organized by:
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GlobalCompliancePanel |
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Invited Speakers:
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Steven S Kuwahara: - 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 . Steve has participated in the development of drugs and biologicals through all phases of clinical research and final product production.
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Deadline for Abstracts:
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2010-12-09
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Registration:
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Tuesday, November 16, 2010
10:00 AM PDT | 01:00 PM EDT | | | Live live online training only for one participant | | |
| | | | | | Corporate Live 4 to 10 participants from a single location (For multiple locations contact Customer Care) | | |
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E-mail:
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webinars@GlobalCompliancePanel.com
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