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Seminar on 21 CFR Part 11 compliance for software validation and SaaS/Cloud

Sao Paulo, Brazil

Thursday, June 22, 2017

 

 

Overview: • This interactive two-day course explores proven techniques for reducing costs associated with implementing, using, and maintaining computer systems in regulated environments. • Many companies are outsourcing IT resources and getting involved with Software as a Service (SaaS) and cloud computing. These vendors are not regulated and therefore regulated companies must ensure compliance for both infrastructure qualification and computer system validation. It is the regulated company that wants to avoid FDA form 483s and warning letters. The seminar is intended for regulated companies, software vendors, and SaaS/Cloud providers. • The instructor addresses the latest computer system industry standards for data security, data transfer, audit trails, electronic records and signatures, software validation, and computer system validation. • Today the FDA performs both GxP and Part 11 inspections, the Europeans have released an updated Annex 11 regulation that expands Part 11 requirements and companies must update their systems and processes to maintain compliance. Location: Sao Paulo, Brazil Date: June 22nd, 23rd, 2017 and Time: 8:30 AM to 5:00 PM Venue: WILL BE ANNOUNCED SOON Price: Price: $1,095.00 (Seminar Fee for One Delegate) Register for 5 attendees Price: $3,285.00 $5,475.00 You Save: $2,190.00 (40%)* Until May 10, Early Bird Price: $1,095.00 From May 11 to June 20, Regular Price: $1,295.00 Quick Contact: NetZealous DBA as GlobalCompliancePanel Phone: 1-800-447-9407 Fax: 302-288-6884 Email: support@globalcompliancepanel.com Website: http://www.globalcompliancepanel.com Registration Link -http://www.globalcompliancepanel.com/control/globalseminars/~product_id=900948SEMINAR?channel=mailer&camp=seminar&AdGroup=wooeb_June_2017_SEO Follow on LinkedIn: https://www.linkedin.com/company/globalcompliancepanel

 

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