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DTSTART:19700308T020000
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UID:2140535:Event:67100
DTSTAMP:20260411T023358Z
SUMMARY:Seminar on Equipment, Facility, and Process Qualification and 
 Validation - A Simple Top to Bottom Sustainable Approach - St. Petersb
 urg, FL
DESCRIPTION:Course \"Equipment, Facility, and Process Qualification an
 d Validation - A Simple Top to Bottom Sustainable Approach\" has been 
 pre-approved byÂ RAPSÂ as eligible for up toÂ 12Â credits towards a pa
 rticipant's RAC recertification upon full completion.\nOverview:\nComp
 anies face many common issues and confusion when creating or revamping
  their validation programs. Some of these common issues are:\n\nCompan
 y has expertise in its process validation program but can never quite 
 get is arms around the facility and equipment changes that require nev
 er ending equipment qualification (IQ, OQ, PQ),\nCustomer or 483 audit
  findings require the company to deviate from its own validation progr
 am to meet the needs of the FDA or the customer\nFor systems that empl
 oy software and hardware, how does the company manage the validation a
 ctivities (i.e. through the software validation effort or through the 
 equipment qualification program?Â \n\n Well, the answers to these and 
 many, many more typical questions are now available in this simple to 
 understand, yet detailed training session designed to help manufacture
 rs of FDA regulated products build (or rebuild) a sustainable validati
 on program.\nWhy should you attend?\nAttend this FDA validation semina
 r to get deep knowledge about:\n\nHow to define a Sustainable Structur
 e of a Firm's Validation Program\nUnderstand How Change Control and Ot
 her Quality Programs Feed Into the Validation Program\nOffer Usable Pr
 otocol and Other Validation Program Document Templates\nDefine Minimal
  Recommended Tests and Verifications for\nEquipment Qualification\nPro
 cess Validation\nSoftware Validation\n\n\nCommon Pitfalls to Avoid Whe
 n Executing Validation Protocols\nHow to Estimate Costs and Time Assoc
 iated with Validation\nHow to Respond to Customer and Regulatory Audit
  Observations Associated with Validation\n\nAreas Covered in the Sessi
 on:\n\nBasics Of Validation\nThe Components of a Sustainable Validatio
 n Program\nOther Programs that Feed the Validation Program (1 Hour)\nE
 quipment, Utility, and Facility Qualification\nProcess Validation\nSof
 tware Validation\nTime and Costs of Validation\nResponding to Validati
 on and Other Related Audit Findings\n\nLocation:Â St. Petersburg, Flor
 ida Date:Â December 3rd & 4th, 2015 Time:Â 9 AM to 6 PMÂ \nÂ \nVenue:Â
  Courtyard St. Petersburg Downtown\nAddress: 300 4th St N, St Petersbu
 rg, Florida 33701, United States\nÂ \nPrice: $1,295.00 (Seminar for On
 e Delegate)\nRegister now and save $200.\nUntil November 15, Early Bir
 d Price:Â $1,295.00\nÂ \nÂ From November 16 to December 01, Regular Pr
 ice:Â $1,495.00\nÂ \nRegistration Details:\nNetZealous LLC - DBA Globa
 lCompliancePanel\n161 Mission Falls Lane, Suite 216, Fremont, CA 94539
 , USAÂ Â Â Â Â Â Â Â Â \nUSA Phone: 1-800-447-9407\nFax: 302-288-6884\
 nsupport@globalcompliancepanel.com Â \nhttp://www.globalcompliancepane
 l.com\nRegistration Link - http://bit.ly/1PR53NH\nÂ \n\nFor more infor
 mation visit https://medtechiq.ning.com/events/seminar-on-equipment-fa
 cility-and-process-qualification-and
DTSTART;TZID=America/New_York:20151203T090000
DTEND;TZID=America/New_York:20151204T180000
CATEGORIES:seminar
LOCATION:Courtyard St. Petersburg Downtown,300 4th St N, St Petersburg
 , FL 33701, United States
WEBSITE:http://bit.ly/1PR53NH
URL:http://bit.ly/1PR53NH
CONTACT:1-800-447-9407
ORGANIZER:NetZealous LLC - DBA GlobalCompliancePanel
ATTACH;FMTTYPE="image/jpeg":http://storage.ning.com/topology/rest/1.0/
 file/get/2562013385?profile=original
ATTENDEE;ROLE=REQ-PARTICIPANT;PARTSTAT=ACCEPTED;RSVP=TRUE;CN="John Rob
 inson":https://medtechiq.ning.com/profile/JohnRobinson
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