Clinasia
Services >> CDISC Services >> ISS/ISE Studies Standardization
     
  ISS/ISE Studies Standardization  
     
 

ClinAsia Labs is highly interested and most considered about the safety and efficacy of the drug under study and is in compliance with CDISC ISS/ISE studies standardization and has proven its services in this area through its strong expertise and experience in this area.

Services include

  • Analysis Plans to enhance Integrated Summaries of Safety and Efficacy
  • Integrated Efficacy and Safe Datasets
  • Integration of data sets to any format
  • Acceptance Coding across studies
  • Data Integration Plan
  • Integrated analysis, reporting Safety and Efficacy of Data
  • Patient Profiles
  • Case Report Tabulation Data Definition Specification
 
     
  CDISC Mapping Specification
Document
 
  SDTM, ADaM Domain Datasets
Generation
 
  Applications Development Using
CDISC Standards
 
  Legacy Study Conversion  
  ISS/ISE Studies Standardization  
  Comprehensive Validation of
SDTM & ADaM Datasets
 
  Define XML Document  
  eCTD Development & Validation  
  CDISC Training  
     
 
 
ClinAsia Labs successfully provided services to a fortune 500 pharma company in the area of clinical data management.

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ClinAsia Labs has provided end to end clinical research services in the field of Neurology to a global pharma company.

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ClinAsia Labs has recently completed a study pathology with its expertise in the areas of EDC and Regulatory affairs for a global pharma company.

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ClinAsia Labs successfully provided services to a fortune 500 pharma company in the area of clinical data management.

-----------------------------------------------
ClinAsia Labs has provided end to end clinical research services in the field of Neurology to a global pharma company.

-----------------------------------------------
ClinAsia Labs has recently completed a study pathology with its expertise in the areas of EDC and Regulatory affairs for a global pharma company.

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