Clinasia
Services >> CDISC Services >> Comprehensive Validation of SDTM & ADaM Datasets
     
  Comprehensive Validation of SDTM & ADaM Datasets  
     
 

ClinAsia Labs relaxes the burden of validation services through its comprehensive range of validation services in compliance with CDISC. This Validation services ensures accuracy, security, safety and efficacy.


Full-cycle Validation
ClinAsia Labs team can provide full cycle validation services as Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) validation tests.


Validation Toolkit
Companies choosing to perform own validation can use ClinAsia Labs Validation Toolkit, a detailed, pre-written IQ and OQ validation test protocols and scripts.


Continuous Development
Company must ensure that its system remains in a constant state of validation. ClinAsia Labs continuously evolves new methods to cut the time involved in validating a system and to make validate software upgrades easy.

 
     
  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.

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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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