Seminar on The DHF, Technical File and Design Dossier - Similarities, Differences and the Future at Las Vegas, NV

Overview:

We will consider the following:

The Design Control requirements of the CGMPs, 21 CFR 820.30

The Design History File - documenting Product Design Control and its nine elements

The Device Master Record and the Device History Record

The EU's Medical Device Directive

The "Essential Requirements"; and their documentation

The remaining elements of a Technical File / Design Dossier

Trends

Two attendee projects

Location: Las Vegas, NV

Venue: Embassy Suites Convention Center Las Vegas, 3600 Paradise Road, Las Vegas, Nevada, 89169, USA

Date: January 14th & 15th, 2016 and Time: 9:00 AM to 6:00 PM

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

Register now and save $200. (Early Bird)

Until November 10, Early Bird Price: $1,295.00 from November 11 to January 12, Regular Price: $1,495.00

Quick Contact:

NetZealous BDA as GlobalCompliancePanel

161 Mission Falls Lane, Suite 216, Fremont, CA 94539, USA.

Phone: 1-800-447-9407

Fax: 302-288-6884

support@globalcompliancepanel.com  

http://www.globalcompliancepanel.com

Registration Link - http://bit.ly/The-DHF-Technical-File-and-Design-Dossier