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:80419
DTSTAMP:20260416T203747Z
SUMMARY:Record Keeping Best Practices [FDA and EMA] Documentation
DESCRIPTION:Overview:Good documentation Practices (GDP) is an essentia
 l factor that needs to be closely followed by the personnel in any reg
 ulated environment as a process for a successful project completion in
 cluding observations of unanticipated responses that are required to b
 e accurately recorded and verified.\nWhy should you Attend:If you are 
 involved in any product manufacturing, knowing GDP regulations is a mu
 st for you. It prevents a lot of errors and minimizes the chance of be
 ing spotted by the regulatory bodies in their audits.\nAreas Covered i
 n the Session:Definition, Purpose, and ImportanceGeneral Rules and Pri
 nciples of GDPRequirements of RecordsGeneral Tips in GDPSignature / in
 itial and the meaningCopying recordsDocument maintenance\nWho Will Ben
 efit:Laboratory Personnel / ManagersValidation SpecialistsClinical Tri
 al PersonnelProject Managers\nSpeaker Profile:Dr. Afsaneh Motamed Khor
 asani PhD is a Medical and scientific Affairs expert and a Senior Scie
 ntist with a strong background in biomedical science and clinical tria
 l/research. She has a tenured and diverse range of experience in medic
 al affairs, basic and industrial clinical research and development, cl
 inical trials, Medical and regulatory writing and intellectual propert
 y.\nEvent Fee: One Dial-in One Attendee Price: US $150.00\nContact Det
 ail:Compliance4All DBA NetZealous,Phone: +1-800-447-9407Email: support
 @compliance4All.com\n\nFor more information visit https://medtechiq.ni
 ng.com/events/record-keeping-best-practices-fda-and-ema-documentation
DTSTART;TZID=America/New_York:20181109T100000
DTEND;TZID=America/New_York:20181109T110000
CATEGORIES:webinar
LOCATION:Online
WEBSITE:https://www.compliance4all.com/control/w_product/~product_id=5
 02168LIVE?channel=medtechiq_Nov_2018_SEO
URL:https://www.compliance4all.com/control/w_product/~product_id=50216
 8LIVE?channel=medtechiq_Nov_2018_SEO
CONTACT:8004479407
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/2562018686?profile=original
ATTENDEE;ROLE=REQ-PARTICIPANT;PARTSTAT=ACCEPTED;RSVP=TRUE;CN="Adam Fle
 ming":https://medtechiq.ning.com/profile/Compliance4all
END:VEVENT
END:VCALENDAR