Phase I Investigational Drug Products | USA Seminar 2018

Overview:

In January 2006, FDA issued a final rule which specified that most pharmaceutical products (including biologics) produced for use in Phase I clinical trial studies were exempted from complying with GMP requirements, as defined in 21 CFR Part 211 under 21 CFR 210.2(c). Section 501(a)(2)(B) of the FD&C Act requires drugs, including IND products, to comply with cGMPs or if they are not manufactured in compliance with cGMPs, they are deemed adulterated. Based on this statutory requirement for manufacturers to follow GMPs, FDA issued cGMP regulations for drug and biological products in the Code of Federal Regulations (in 21 CFR parts 210 and 211).

Location:  Salt Lake City, UT Date: May 10th & 11th, 2018  and Time: 9:00 AM to 6:00 PM

Venue:  Hilton Garden Inn Salt Lake City Airport   4975 Wiley Post Way, Salt Lake City, Utah, 84116, USA

Price:

Price: $1,295.00 (Seminar Fee for One Delegate)

Register for 5 attendees Price: $3,885.00 $6,475.00 You Save: $2,590.00 (40%)*

Register for 10 attendees Price: $7,122.00 $12,950.00 You Save: $5,828.00 (45%)*

Register now and save $200. (Early Bird)

Until March 31, Early Bird Price: $1,295.00 From April 01 to May 7, Regular Price: $1,495.00

Sponsorship Program benefits for “Phase I Investigational Drug Products | USA Seminar 2018” seminar

For More Information- https://www.globalcompliancepanel.com/control/sponsorship 

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