Time: November 9, 2017 at 9am to November 10, 2017 at 6pm
Location: Seoul, South Korea
Street: Seoul, South Korea
City/Town: Seoul, South Korea
Website or Map: http://www.globalcompliancepa…
Event Type: online, healthcare, training, courses
Organized By: NetZealous DBA as GlobalCompliancePanel
Latest Activity: Sep 14, 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.
Location: Seoul, South Korea Date: November 9th & 10th, 2017 and Time: 9:00 AM to 6:00 PM
Venue: WILL BE ANNOUNCED SOON, Seoul, South Korea
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 07, 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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NetZealous LLC DBA GlobalCompliancePanel
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