Clinasia
Services >> CDISC Services >> Applications Development Using CDISC Standards
     
  Applications Development Using CDISC Standards  
     
 

ClinAsia Labs with its vast experience and knowledge in detail of the clinical trial process provides application development services with a blend of information technology. It has proven expertise in this area in compliance with CDISC Standards.

 

 
 

The services include

Study Planning

  • Planning a Project
  • Installation planning
  • Configuration planning
  • Validation planning
  • Infrastructure planning
  • Architecture planning

Design and Development

  • Installation
  • Configuration
  • Validation
  • Design and development of a standard forms

Deployment

  • Training

  • Study monitoring and support

  • Integration of Data and Procedures

Maintenance and Support

  • Upgrade and data migration

  • 24x7 global support

 
     
     
  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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