Clinasia
Services >> Phase II-IIIb
     
  Phase II-IIIb  
     
 

We advance a product through development and approval on time and within a client's budget. Our experienced teams deliver quality results for our clients' drug development needs.

Development Consulting
Our strategic product development solutions offer our clients the best long-term strategies for their products. We help our clients reach key milestones in a timely and cost-effective way while minimizing risks by designing, planning and implementing high quality, strategic product development programs.

Data Management
ClinAsia Labs provides data management expertise and comprehensive data management services for Phase I-IV clinical trials. The data management planning process emphasizes close communication with the sponsor through all phases of development and review of database specifications.

Quality Assurance
ClinAsia Labs staff is accessible and responsive to questions and requests for information during any part of a study. We provide an independent assessment of the client's quality assurance procedures, based on Good Clinical Practices, regulatory requirements in drug development projects.

Project Management
Our project team ensures deliverables on-time and on-cost, resulting in effective Phase programs. Your people will be fully trained in the therapeutic area being studied and possess a remarkable ability to anticipate risks and finish of the study on a clearly visible success note.


Clinical Monitoring
As always our clinical monitoring teams deliver quality, timely results. Counting by therapeutic industry experience with which ClinAsia Labs provides consistent, effective and interactive dialogue at the sites.

Safety and Pharmacovigilance
Through our customized safety plan we provide comprehensive safety coverage round the clock. We ensure safety by maintaining clinical safety databases, effective monitoring through coordination of data monitoring committees and also using effective alerting system which is automated with a signal alarming system.

Patient Recruitment
Effectively designed programs help ensure that ClinAsia Labs will generate the calls needed to meet your enrollment targets.

Biostatistics
We provide biostatistics consultation, programming, and analyses. Software used includes SAS, StatXact, nQuery Advisor, and other cutting-edge products.

Regulatory Affairs
ClinAsia Labs ’s regulatory affairs staff provides flexible and responsive services according to your needs, ClinAsia Labs regulatory affairs team assists you in meetings with regulatory authorities provide scientific advice and define a regulatory strategy.

 
     
     
  Development Consulting  
  Data Management  
  Quality Assurance  
  Project Management  
 

Clinical Monitoring

 
  Safety and Pharmacovigilance  
  Patient Recruitment  
  Biostatistics  
  Regulatory Affairs  
     
 
 
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.

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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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