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DTSTART;VALUE=DATE:20250101
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DESCRIPTION:Date:&nbsp\;Tuesday 14th &amp\; Wednesday 15th November 2023\nT
 ime:&nbsp\;09:00-17:00 each day\nLocation:&nbsp\;This Course will be taugh
 t in person\, at De Morgan House\, 57-58 Russell Square\,&nbsp\;London WC1
 B 4HS\nSpeaker:&nbsp\;Professor Steven A Julious&nbsp\;(Section Director a
 nd NIHR Senior Investigator at The University of Sheffield.)\n\nWho is thi
 s event intended for?&nbsp\;Statisticians working in clinical trials looki
 ng to learn about sample size calculations for different types of trial ou
 tcomes and study objectives.\nWhat is the benefit of attending?&nbsp\;The 
 study is a practical course based on real world calculations where partici
 pants will be able to come away understanding how to calculate their own s
 ample sizes depending on the type of clinical trial design. Participants w
 ill also be introduced to how some estimates used in the calculations are 
 obtained. There will be an opportunity for attendees also to meet and netw
 ork with other attendees across the industry.\nCost\n PSI Members&nbsp\;= 
 &pound\;320+VAT\nNon-Members&nbsp\;= &pound\;430*+VAT\n*Please note:&nbsp\
 ;Non-Member rates include PSI membership until 31 Dec. 2024.\n\nRegistrati
 on\nTo book your place\, please&nbsp\;click here.&nbsp\;\nPlease note:\n- 
 There are a limited number of places for this in-person event. Due to its 
 popularity\, we do kindly ask you to consider both the timings and locatio
 n before committing to attend.\n-&nbsp\;Registration does not include hote
 l accommodation.&nbsp\;If a hotel is required (as this Course runs over tw
 o consecutive days)\, delegates will need to book their own accommodation 
 separately. Some hotels local to the venue are:&nbsp\;President Hotel\, Be
 auchamp Hotel\, Mercure and Imperial Hotels.\n\nOverview\nThe three most i
 mportant aspects of a clinical trial are: design\, design and design. A sa
 mple size estimate is just one aspect of a clinical study design. The cour
 se describes calculations for sample size estimation in the design of clin
 ical trials. It will highlight how the objectives of a clinical trial will
  impact on sample size calculations. The course is a practical course and 
 all methods will be illustrated with examples and case studies.\nAgenda\nT
 here will be 4 sessions per day\, each between 1.30-2.00 hours. A session 
 will consist of both lectures and practicals\, involving calculators or ot
 her calculation devices.&nbsp\;\nDay 1\nAfter introductions&nbsp\;the cour
 se will give a background to sample size calculations and then go on to co
 ver sample sizes in superiority trials with Normal and binary data\, endin
 g the day with trials based on precision. Each lecture will be based on a 
 hands on practical of the methods.\nDay 2\nThe day will begin with&nbsp\;s
 ample sizes for cross-over trials followed by a practical which will also 
 enforce the lessons from day 1. The course will then cover calculations fo
 r non-inferiority and equivalence trials as well as trials with ordinal da
 ta and trials with survival data. It will then move on to more advanced to
 pics of sample sizes for pilot trials and the design of trials which will 
 be adaptive\, ending the day with further statistical considerations in th
 e design of studies.\nPresenter details\n\n\n\n    \n        \n           
  \n            Speaker\n            \n            \n            Biography\
 n            \n        \n        \n            \n            \n           
  \n            \n            Steven A Julious\, Professor of Medical Stati
 stics\, has over 30 years of applied experience in medical statistics in b
 oth industry and the academic setting with an interest in all aspects of c
 linical trials from molecule through to the marketplace. His main research
  focus is clinical trial design and the development of applied methods rel
 ated to clinical trials. The methodologies around sample size estimation a
 re a particular interest and as well as a book\, the second edition of whi
 ch has just been published\, Steven has developed a mobile app for the cal
 culations called SampSize.\n            \n        \n    \n
DTEND:20231115T170000Z
DTSTAMP:20260812T020751Z
DTSTART:20231114T090000Z
LOCATION:
SEQUENCE:0
SUMMARY:PSI Training Course: Sample Sizing for Clinical Trials
UID:RFCALITEM639220972710666662
X-ALT-DESC;FMTTYPE=text/html:<strong>Date:</strong>&nbsp\;Tuesday 14th &amp
 \; Wednesday 15th November 2023<br />\n<strong>Time:</strong>&nbsp\;09:00-
 17:00 each day<br />\n<strong>Location:</strong>&nbsp\;<span style="text-d
 ecoration: underline\; color: #ff0000\;">This Course will be taught <stron
 g>in person</strong></span>\, at De Morgan House\, 57-58 Russell Square\,&
 nbsp\;London WC1B 4HS<br />\n<strong>Speaker:</strong>&nbsp\;Professor Ste
 ven A Julious&nbsp\;<em>(Section Director and NIHR Senior Investigator at 
 The University of Sheffield.)</em><br />\n<br />\n<strong>Who is this even
 t intended for?</strong>&nbsp\;Statisticians working in clinical trials lo
 oking to learn about sample size calculations for different types of trial
  outcomes and study objectives.<br />\n<strong>What is the benefit of atte
 nding?</strong>&nbsp\;The study is a practical course based on real world 
 calculations where participants will be able to come away understanding ho
 w to calculate their own sample sizes depending on the type of clinical tr
 ial design. Participants will also be introduced to how some estimates use
 d in the calculations are obtained. There will be an opportunity for atten
 dees also to meet and network with other attendees across the industry.<br
  />\n<h4>Cost</h4>\n<p><strong> PSI Members</strong>&nbsp\;= &pound\;320+V
 AT<br />\n<strong>Non-Members</strong>&nbsp\;= &pound\;430*+VAT<br />\n*<e
 m>Please note:&nbsp\;Non-Member rates include PSI membership until 31 Dec.
  2024.<br />\n</em></p>\n<h4>Registration</h4>\n<p>To book your place\, pl
 ease&nbsp\;<strong><a href="https://psi.glueup.com/event/psi-training-cour
 se-sample-sizing-for-clinical-trials-84301/" target="_blank">click here</a
 ></strong>.&nbsp\;<br />\n<strong><span style="text-decoration: underline\
 ;"><em>Please note</em></span></strong><em>:<br />\n- There are a limited 
 number of places for this in-person event. Due to its popularity\, we do k
 indly ask you to consider both the timings and location before committing 
 to attend.<br />\n-&nbsp\;<strong>Registration does not include hotel acco
 mmodation.&nbsp\;</strong>If a hotel is required (as this Course runs over
  two consecutive days)\, delegates will need to book their own accommodati
 on separately. Some hotels local to the venue are:&nbsp\;President Hotel\,
  Beauchamp Hotel\, Mercure and Imperial Hotels.<br />\n</em></p>\n<h4>Over
 view</h4>\n<p>The three most important aspects of a clinical trial are: de
 sign\, design and design. A sample size estimate is just one aspect of a c
 linical study design. The course describes calculations for sample size es
 timation in the design of clinical trials. It will highlight how the objec
 tives of a clinical trial will impact on sample size calculations. The cou
 rse is a practical course and all methods will be illustrated with example
 s and case studies.</p>\n<h4>Agenda</h4>\n<p>There will be 4 sessions per 
 day\, each between 1.30-2.00 hours. A session will consist of both lecture
 s and practicals\, involving calculators or other calculation devices.&nbs
 p\;</p>\n<h5><span style="text-decoration: underline\;">Day 1</span></h5>\
 n<p>After introductions&nbsp\;the course will give a background to sample 
 size calculations and then go on to cover sample sizes in superiority tria
 ls with Normal and binary data\, ending the day with trials based on preci
 sion. Each lecture will be based on a hands on practical of the methods.</
 p>\n<h5><span style="text-decoration: underline\;">Day 2</span></h5>\n<p>T
 he day will begin with&nbsp\;sample sizes for cross-over trials followed b
 y a practical which will also enforce the lessons from day 1. The course w
 ill then cover calculations for non-inferiority and equivalence trials as 
 well as trials with ordinal data and trials with survival data. It will th
 en move on to more advanced topics of sample sizes for pilot trials and th
 e design of trials which will be adaptive\, ending the day with further st
 atistical considerations in the design of studies.</p>\n<h4>Presenter deta
 ils</h4>\n<table border="1" cellspacing="0" cellpadding="0">\n</table>\n<t
 able class="table table-striped table-bordered">\n    <tbody>\n        <tr
 >\n            <td valign="top" style="width: 104px\;">\n            <p><s
 trong>Speaker</strong></p>\n            </td>\n            <td valign="top
 " style="width: 497px\;">\n            <p><strong>Biography</strong></p>\n
             </td>\n        </tr>\n        <tr>\n            <td valign="to
 p" style="width: 104px\;">\n            <p><img src="https://www.psiweb.or
 g/images/default-source/default-album/stevenedit.png?sfvrsn=5705addb_0&sf_
 site_temp=true&sf_site=00000000-0000-0000-0000-000000000000" data-displaym
 ode="Original" alt="Stevenedit" title="Stevenedit" /></p>\n            </t
 d>\n            <td valign="top" style="width: 497px\;">\n            <p>S
 teven A Julious\, Professor of Medical Statistics\, has over 30 years of a
 pplied experience in medical statistics in both industry and the academic 
 setting with an interest in all aspects of clinical trials from molecule t
 hrough to the marketplace. His main research focus is clinical trial desig
 n and the development of applied methods related to clinical trials. The m
 ethodologies around sample size estimation are a particular interest and a
 s well as a book\, the second edition of which has just been published\, S
 teven has developed a mobile app for the calculations called SampSize.</p>
 \n            </td>\n        </tr>\n    </tbody>\n</table>
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