ComplianceOnline

GMP Expectations for Products Used in Early Phase IND Studies

Instructor: Steven S Kuwahara
Product ID: 701009
  • Duration: 75 Min

recorded version

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Last Recorded Date: Nov-2008

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Read Frequently Asked Questions

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.

Description

This presentation will be aimed at helping Regulatory, Quality Assurance and Quality Control personnel to understand the varying levels of quality activities that accompany early stages of Product development.

FDA has issued a guidance document covering GMP requirements for products that will be used in early stage clinical studies. These guidelines are in addition to those that cover the CMC sections for IND submissions at Phase 1. The nature and extent of the GMP activities 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 seminar:

  • Discussion of the elements to be found in the key 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.
  • Which regulations come into play at different stages of product development.
  • 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 levels of quality 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
  • R & D personnel who will contribute data to CMC sections
  • Project managers for product development studies
  • Quality systems auditors
  • Consultants

Instructor 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 . He has participated in the product development process for small molecule drugs and biologics, and has prepared or reviewed many CMC sections.

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Registrants may cancel up to two working days prior to the course start date and will receive a letter of credit to be used towards a future course up to one year from date of issuance. ComplianceOnline would process/provide refund if the Live Webinar has been cancelled. The attendee could choose between the recorded version of the webinar or refund for any cancelled webinar. Refunds will not be given to participants who do not show up for the webinar. On-Demand Recordings can be requested in exchange.

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