Clinasia
Services >> Phase I
     
  Phase I  
     
 

ClinAsia Labs Phase I services is treated as one of the best in the world with the proven ability to carry out multiple studies in parallel, and our services span over from healthy volunteer clinics to regulatory affairs. ClinAsia Labs ability to successfully facilitate large trials along with our committed, experienced experts enables effective planning strategy and implementation for the first phase of clinical trials.


Research Clinic
Created specially to enhance first-phase trials, ClinAsia Labs research clinic has a huge range of specialized technology facility for storing and handling, administering and monitoring new drugs being planned for development. Taking into account the clinical expertise ClinAsia Labs possess ClinAsia Labs deals with the studies such as First Administration into human, Bioequivalence, Bioavailability, Ascending dose safety, Drug interaction at macro level.

 

Clinical Monitoring
ClinAsia Labs expert trained Associates ensure the ultimate quality review of data and improved interaction with study sites. ClinAsia Labs clinical research associates during their monitoring makes sure to see over data collection, view source documentation, case report forms, regulatory compliance, solve data queries and implement interim analyses.

 

Project management
ClinAsia Labs from its vast experience in the past learns that project manager is the captain made responsible for the successful functioning of a trial and it’s his responsibility to ensure that the project is on time and on budget. ClinAsia Labs assigns one of our super senior experts and shall be made a point of responsibility as well as a point of contact for all future interactions till the close of the study.

 

Data Management
ClinAsia Labs provides data management expertise and comprehensive data management services for all phases of clinical trials. The data management planning process symbolizes regular communication with the sponsor through every phase of development and review database specifications. Quality control mechanisms monitor every element of the data management process, and ClinAsia Labs helps minimize the client's technology investment through guidance in the most effective use of appropriate technology according to the sponsor's particular needs and preferences.

 

Biostatistics
ClinAsia Labs provides biostatistician consultation, analyses and programming. Software which would be for this purpose includes SAS, StatXact, nQuery Advisor, and other leading marketing edge products.

 

Pharmacovigilance
Through ClinAsia Labs customizable safety plan we provide efficient safety coverage round the clock. ClinAsia Labs ensures safety by effective monitoring through coordination of data monitoring committees, maintaining clinical safety databases and also using innovative alerting system which is automated with a alarming system.

 

Regulatory Services
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

 
     
     
  Research Clinic  
  Clinical Monitoring  
  Project Management  
  Data Management  
 

Biostatistics

 
  Pharmacovigilance  
  Regulatory Services  
     
 
 
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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