BEGIN:VCALENDAR
VERSION:2.0
PRODID:icalendar-ruby
CALSCALE:GREGORIAN
BEGIN:VEVENT
DTSTAMP:20240329T154528Z
UID:8f47245c-1269-4c44-adf3-7e276daf830c
DTSTART:20211021T070000
DTEND:20211022T070000
CLASS:PRIVATE
DESCRIPTION:\n
\n
The 2020 Endpoint Adjudication Forum is an advanced conference on endpoi
nt adjudication. Over the course of this beyond-the-basics forum\, attende
es will 1) analyze strategies to craft a charter\; 2) discuss principles f
or \;instituting a Clinical Endpoint Committee (CEC)\; 3) scrutinize p
rocedures for capturing\, managing and monitoring data\; and 4) look at gu
idance documents for adjudication.
\n\n
Through networking\, case studies and panel discussions\, professional
s from biotech\, pharmaceutical and medical device companies will return t
o work with the necessary tools and acumen to enhance and streamline endpo
int adjudication. This conference will feature an embedded master class on
the first morning of the conference\, which will clarify the fundamentals
of endpoint adjudication.
\n\n
With
two days of educational content and ample networking time\, the 2020 
\;Endpoint Adjudication Forum is a must-attend event for professionals aim
ing to adapt and otherwise improve upon endpoint adjudication best practic
es.
\n\n
Top Five Reasons to Attend
\n\n
\n - L
earn to balance the FDA&rsquo\;s regulatory requests and demands with the
practicality of performing a CEC for a trial
\n - Establish guidance documents for adjudication
\n - Enhance trial integrity
and prepare data for adjudication submission and approval
\n <
li style="outline: 0px\; margin: 10px 0px 10px 35px\; padding: 0px 0px 0px
15px\; border: 0px\; font-style: inherit\; font-variant: inherit\; font-w
eight: inherit\; font-stretch: inherit\; font-size: inherit\; line-height:
inherit\; font-family: inherit\; vertical-align: baseline\; list-style: c
ircle\;">Analyze inconsistencies in adjudica
tion data sets while learning to construct an effective database\n - Comply with regulations throu
gh standard submissions
\n
\n\n
Who Should Attend
\n\n
This conference is designed for professionals in b
iotech\, pharmaceutical and medical device companies with responsibilities
in the following areas:
\n\n
\n
- Medical/Clinical Safety
\n - Medical/Scientific Affairs
\n - Clinical Operations
\n - Event Adjudication
\n - Biostatistics
\n - Pharmacovigilance
\
n - Protocol Management
\
n - Clinical Monitoring
\
n - Data Management
\n Electronic Data Capture\
n - Clinical Development
\n - Project/Trial Management
\n - Regulatory
\n <
li style="outline: 0px\; margin: 10px 0px 10px 35px\; padding: 0px 0px 0px
15px\; border: 0px\; font-style: inherit\; font-variant: inherit\; font-w
eight: inherit\; font-stretch: inherit\; font-size: inherit\; line-height:
inherit\; font-family: inherit\; vertical-align: baseline\; list-style: c
ircle\;">Study Design\n - Informatics
\n - Safety \;Operations
\n Medical Products \;Safety \n\n
\n