BEGIN:VCALENDAR
VERSION:2.0
PRODID:www.eu-parc.eu
BEGIN:VEVENT
UID:6af0b8fb98062
DTSTART:20261204T100000Z
SEQUENCE:0
TRANSP:OPAQUE
DTEND:20261204T110000Z
SUMMARY:Webinar on data reporting and acceptability in chemical analysis
CLASS:PUBLIC
DESCRIPTION:As part of the webinar series on quality assurance (QA) and qua
 lity control (QC) in chemical analysis and in vitro toxicity testing\, PAR
 C will host a webinar on data reporting and acceptability in chemical anal
 ysis\, which will take place online\, via Microsoft Teams on 4 December 20
 26\, from 11:00 to 12:00 CET. The session will be led by Emmanuelle Bichon
  from Oniris VetAgroBio ↗ (LABERCA\, France) and Françoise Schaefers fr
 om the National Health Laboratory of Luxembourg ↗ (LNS\, Luxembourg).Wha
 t to expect:This webinar will present the reporting requirements and data 
 acceptability approach set out in the PARC guidance document D9.4-1. Parti
 cipants will learn which information should go with analytical results so 
 that data can be interpreted correctly\, traced back to their source and c
 ompared across laboratories\, from sampling through to the final result. T
 he first part of the webinar will provide an overview of the mandatory and
  optional reporting items and explain their requirements. The second part 
 will focus on assessing data acceptability using an indicator-based calcul
 ation.Who should attend:This session is open to researchers\, laboratory a
 nalysts\, quality managers\, project leaders\, data managers and data user
 s (e.g. exposure and risk assessors) working with chemical analysis data\,
  both within and outside PARC. Participants should have a basic understand
 ing of analytical chemistry and QA/QC concepts.Practical details:Participa
 tion in this webinar is free of charge. Places are limited and will be all
 ocated on a first-come\, first-served basis. Registered participants will 
 receive the connection link after registration.Application deadline:The re
 gistration form will remain open until the maximum capacity of 300 partici
 pants is reached or until 1 December 2026\, whichever comes first.How to a
 pply:To participate\, please complete the registration form here ↗.Stay 
 informed about upcoming webinars on QA/QC in chemical analysis and in vitr
 o toxicity testing by following the PARC website and social media channels
 !
X-ALT-DESC;FMTTYPE=text/html:<!doctype html><html><body><p style=\"margin-b
 ottom:20px\;\">As part of the webinar series on quality assurance (QA) and
  quality control (QC) in chemical analysis and <em>in vitro</em> toxicity 
 testing\, PARC will host a webinar on data reporting and acceptability in 
 chemical analysis\, which will take place online\, via Microsoft Teams on 
 4 December 2026\, from 11:00 to 12:00 CET. The session will be led by Emma
 nuelle Bichon from <a href=\"https://www.oniris-nantes.fr/en/\">Oniris Vet
 AgroBio<span class=\"external-link-mark\"> ↗</span></a> (LABERCA\, Franc
 e) and Françoise Schaefers from the <a href=\"https://lns.lu/en/\">Nation
 al Health Laboratory of Luxembourg<span class=\"external-link-mark\"> ↗<
 /span></a> (LNS\, Luxembourg).</p><p style=\"margin-bottom:5px\;\"><strong
 >What to expect:</strong></p><p style=\"margin-bottom:20px\;\">This webina
 r will present the reporting requirements and data acceptability approach 
 set out in the PARC guidance document D9.4-1. Participants will learn whic
 h information should go with analytical results so that data can be interp
 reted correctly\, traced back to their source and compared across laborato
 ries\, from sampling through to the final result. The first part of the we
 binar will provide an overview of the mandatory and optional reporting ite
 ms and explain their requirements. The second part will focus on assessing
  data acceptability using an indicator-based calculation.</p><p style=\"ma
 rgin-bottom:5px\;\"><strong>Who should attend:</strong></p><p style=\"marg
 in-bottom:20px\;\">This session is open to researchers\, laboratory analys
 ts\, quality managers\, project leaders\, data managers and data users (e.
 g. exposure and risk assessors) working with chemical analysis data\, both
  within and outside PARC. Participants should have a basic understanding o
 f analytical chemistry and QA/QC concepts.</p><p style=\"margin-bottom:5px
 \;\"><strong>Practical details:</strong></p><p style=\"margin-bottom:20px\
 ;\">Participation in this webinar is free of charge. Places are limited an
 d will be allocated on a first-come\, first-served basis. Registered parti
 cipants will receive the connection link after registration.</p><p style=\
 "margin-bottom:5px\;\"><strong>Application deadline:</strong></p><p style=
 \"margin-bottom:20px\;\">The registration form will remain open until the 
 maximum capacity of 300 participants is reached or until 1 December 2026\,
  whichever comes first.</p><p style=\"margin-bottom:5px\;\"><strong>How to
  apply:</strong></p><p style=\"margin-bottom:15px\;\">To participate\, ple
 ase complete the registration form <a href=\"https://forms.cloud.microsoft
 /Pages/ResponsePage.aspx?id=CEbIIh3wxUaAJGPMli5fUYwTPje3_CFHuPW5W0P0dA5UQl
 o1MDRETDVEOFpNN1pZRVE5Mk82RUdYUC4u\">here<span class=\"external-link-mark\
 "> ↗</span></a>.</p><p style=\"margin-bottom:20px\;\">Stay informed abou
 t upcoming webinars on QA/QC in chemical analysis and <em>in vitro</em> to
 xicity testing by following the PARC website and social media channels!</p
 ></body></html>
DTSTAMP:20261108T180131Z
END:VEVENT
END:VCALENDAR