BEGIN:VCALENDAR PRODID:NingEventWidget-v1 VERSION:2.0 METHOD:PUBLISH BEGIN:VTIMEZONE TZID:America/New_York X-LIC-LOCATION:America/New_York BEGIN:DAYLIGHT TZOFFSETFROM:-0500 TZOFFSETTO:-0400 TZNAME:EDT DTSTART:19700308T020000 RRULE:FREQ=YEARLY;BYMONTH=3;BYDAY=2SU END:DAYLIGHT BEGIN:STANDARD TZOFFSETFROM:-0400 TZOFFSETTO:-0500 TZNAME:EST DTSTART:19701101T020000 RRULE:FREQ=YEARLY;BYMONTH=11;BYDAY=1SU END:STANDARD END:VTIMEZONE BEGIN:VEVENT UID:2140535:Event:67835 DTSTAMP:20260411T180230Z SUMMARY:Webinar on Validation Master Planning and Regulatory Expectati ons DESCRIPTION:Overview: Our Speaker will explain the expectations of re gulatory authorities both domestic and international. You should atten d if you are not familiar with the activity or would like to understan d the expectations both foreign and domestic.\nThis presentation will cover the importance of master planning. The FDA and other regulatory bodies expect these to be among the Quality System documentation. Ho w best should it be implemented and maintained? What are the types and how many should there be? This presentation will delve into the detai l of development and presentation. It will also cover some of the do's and don'ts as well as view point of an auditor. Areas Covered in the Session:\n\nHistory and background\nTypes\nOrganization\nRequirements \nRegulatory expectations\nMaintenance\nUse\nUpkeep\nPICs guideline\n2 011 requirements\nDo's and don'ts\n\nWho Will Benefit:\n\nCompliance P ersonnel\nQA Personnel\nvalidation Personnel\n\nSpeaker Profile:\n\nLo uis Angelucci is a pharmaceutical professional and Certified Quality Engineer with over 20 years of experience in Quality Assurance, Qualit y Control, Validation, consent decree remediation as well as cGMP Comp liance in the Medical Device and Pharmaceutical industries. Lou has wo rked for several well know companies inclusive of Johnson & Johnson, B ristol-Meyer Squibb, Pfizer, Schering Plough and Merck. This work expe rience was acquired either as a direct employee or as a contracting co nsultant while employed at Foster Wheeler and Aker Kvaerner. As a cons ultant Lou has worked at various project locations both domestically a nd overseas. Lou is a member of the IVT board of Directors and has bee n a contributing speaker to IVT since the organization’s early begin nings. He has published numerous articles on the subjects of Validatio n and compliance and has been a speaker to industry groups such as ISP E, IDE, PDA and ASQ. \nContact Detail:\nNetZealous - Compliance4All,1 61 Mission Falls Lane, Suite 216,Fremont, CA 94539, USA.Phone: +1-800- 447-9407Email: support@compliance4All.comhttp://www.compliance4all.com /Event Link : http://bit.ly/Validation_Master_Planning\n\n\n\nFor mor e information visit https://medtechiq.ning.com/events/webinar-on-valid ation-master-planning-and-regulatory-expectations DTSTART;TZID=America/New_York:20160303T100000 DTEND;TZID=America/New_York:20160303T110000 CATEGORIES:webinar LOCATION:Online Event WEBSITE: URL: CONTACT:Event Manager ORGANIZER;CN="Adam Fleming":https://medtechiq.ning.com/profile/Complia nce4all ATTACH;FMTTYPE="image/jpeg":http://storage.ning.com/topology/rest/1.0/ file/get/2562012364?profile=original ATTENDEE;ROLE=REQ-PARTICIPANT;PARTSTAT=ACCEPTED;RSVP=TRUE;CN="Adam Fle ming":https://medtechiq.ning.com/profile/Compliance4all END:VEVENT END:VCALENDAR