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      GMP and Regulatory Expectations for Early IND Products 2017

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      November 13, 2017 - November 14, 2017

      Monday   9:00 AM - Tuesday 6:00 AM (daily until November 14, 2017)

      Taipei, Taiwan

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      GMP and Regulatory Expectations for Early IND Products 2017

      Course "GMP and Regulatory Expectations for Early IND Products" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion.


      This course will present, in one place, the regulations and guidelines that apply to early phase products. In some cases these will not be regulations, but needs that, if met, will increase the efficiency of activities as a product proceeds through the development process. The course will present these items in the order of product development from the point of R & D activities to the completion of Phase 2 clinical trials.

      Why should you attend:

      Any pharmaceutical worker who must deal with products both in early and latter phases of development should attend this course in order to be aware of the regulatory requirements that will affect operations dealing with these products. The modifications to the GMPs for early phase products have modified the GMPs in such a way as to reduce requirements to allow more efficient work. At the same time some of the things that may appear to have changed, have not, and the pharmaceutical worker should be aware of this.

      Who will benefit:

      • Directors, Managers, Supervisors, and lead workers in Regulatory Affairs, Quality Assurance and Quality Control
      • Workers who will prepare GMP documents for early phase products as well as those who will review these documents
      • Regulatory affairs workers who will need to deal with submissions covering early phase products

      Day 1 Schedule

      Lecture 1:
      Very Early Stages
      • The need for documentation of matters that will affect downstream work.
      • The effects of ICH Q8
      o Impact on R & D activities
      o Risk analysis and design control at this stage.
      Lecture 2:
      GLP requirements
      • Animal studies
      o Toxicology and pharmacokinetics.
      • Estimating the Maximum Safe Starting Dose
      o A review of the guidance document.
      Lecture 3:
      Early Pre-IND Studies
      • Understanding exploratory Studies
      o Definitions and the IND that will be withdrawn.
      • Orphan Drugs
      • Drugs studied under the Animal Rule
      o What they are and how to conduct the studies.
      Lecture 4:
      Meetings and Preparing for the IND
      • Information required for the Phase 1 IND
      o The CMC requirements that will be needed.
      • Pre-IND Meetings with FDA

      Day 2 Schedule

      Lecture 1:
      GMPs for Phase 1 IND products
      • The scope of the guidance document
      • The second guidance document covering the GMPs.
      Lecture 2:
      GMPs for Phase 1 continued
      • A presentation covering what GMPs are required at this stage.
      • What has been omitted from the GMPs for Phase 1.
      Lecture 3:
      Requirements for Phase 2 INDs
      • The full GMPs resume, but do they?
      • Phase 2 studies and the transition to full GMPs.
      • CMC requirements.
      Lecture 4:
      Preparing for IND Meetings
      • Phase 1 meetings
      • Pre-phase 2 meetings
      • Phase 2 meetings

      Dr. Steven Kuwahara
      Founder & Principal, GXP Biotechnology, LLC

      Dr. Steven 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.

      Location: Taipei, Taiwan Date: November 13th & 14th, 2017 and Time: 9:00 AM to 6:00 PM
      Venue: WILL BE ANNOUNCED SOON , Taipei, Taiwan

      Price: $895.00 (Seminar Fee for One Delegate)
      Register for 5 attendees Price: $2,685.00 $4,475.00 You Save: $1,790.00 (40%)*
      Register now and save $200. (Early Bird)
      Until October 05, Early Bird Price: $895.00 From October 06 to November 11, Regular Price: $1,095.00
      Register for 10 attendees Price: $4,922.00 $8,950.00 You Save: $4,028.00 (45%)*

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      At this seminar, world-renowned FDA Regulated Industry subject matter experts interact with CXO’s of various designations. Executives who carry vast experience about FDA Regulated Industry and Experts get down to discussing industry-related best practices, regulatory updates, changes in technologies, and much more relating to FDA Regulated Industry.
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      Cost: Payment required - Price: $895.00 (Seminar Fee for One Delegate) Register for 5 attendees Price: $2,685.00 $4,475.00 You Save: $1,790.00 (40%)* Register for 10 attendees Price: $4,922.00 $8,950.00 You Save: $4,028.00 (45%)* Register now and save $200. (Early Bird) ? Enroll

      Categories: Education | Health & Wellness | Technology

      This event repeats daily until November 14, 2017:

      Event details may change at any time, always check with the event organizer when planning to attend this event or purchase tickets.
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