{"title":"准备一个基于多个试验的电子提交,其中一些是正在进行的统计程序的挑战","authors":"Åsa Carlsheimer","doi":"10.1179/175709311X13141790413200","DOIUrl":null,"url":null,"abstract":"AbstractPreparing for an eSubmission based on multiple trials, some of which are ongoing, is a challenging task for statistical programmers. Having Analysis Data Model (ADaM) standards in place and maintaining a pooled data repository will facilitate the submission work on the data side. However, generating more than 1100 tables and figures for the Integrated Summary of Safety and Efficacy, involving a large team of biostatisticians and statistical programmers (in-house and off-shore), requires careful planning that includes preliminary discussions on consistency across programs. The purpose of this paper is to share experiences and provide some advice for statistical programmers to consider in future submission work.","PeriodicalId":253012,"journal":{"name":"Pharmaceutical Programming","volume":"49 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2011-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Preparing an eSubmission based on multiple trials, some of which are ongoing — challenges for statistical programming\",\"authors\":\"Åsa Carlsheimer\",\"doi\":\"10.1179/175709311X13141790413200\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"AbstractPreparing for an eSubmission based on multiple trials, some of which are ongoing, is a challenging task for statistical programmers. Having Analysis Data Model (ADaM) standards in place and maintaining a pooled data repository will facilitate the submission work on the data side. However, generating more than 1100 tables and figures for the Integrated Summary of Safety and Efficacy, involving a large team of biostatisticians and statistical programmers (in-house and off-shore), requires careful planning that includes preliminary discussions on consistency across programs. The purpose of this paper is to share experiences and provide some advice for statistical programmers to consider in future submission work.\",\"PeriodicalId\":253012,\"journal\":{\"name\":\"Pharmaceutical Programming\",\"volume\":\"49 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2011-12-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Pharmaceutical Programming\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1179/175709311X13141790413200\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pharmaceutical Programming","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1179/175709311X13141790413200","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Preparing an eSubmission based on multiple trials, some of which are ongoing — challenges for statistical programming
AbstractPreparing for an eSubmission based on multiple trials, some of which are ongoing, is a challenging task for statistical programmers. Having Analysis Data Model (ADaM) standards in place and maintaining a pooled data repository will facilitate the submission work on the data side. However, generating more than 1100 tables and figures for the Integrated Summary of Safety and Efficacy, involving a large team of biostatisticians and statistical programmers (in-house and off-shore), requires careful planning that includes preliminary discussions on consistency across programs. The purpose of this paper is to share experiences and provide some advice for statistical programmers to consider in future submission work.