FDA compliant Bioanalytical Contract
Research Organization (CRO)
 
.Professional service
.Meet Deadlines
.Cost-effective Budgets
 
 
     
   
 
Sannova Analytical Inc. (SAI) is a GXP compliant Bioanalytical Contract Research Organization (CRO) located in central New Jersey, USA.

Sannova’s experienced scientists provide Bioanalytical services from the method development and validation through delivery of Bioequivalence/Bioavailability (BA/BE) or Pharmacokinetic/Toxicokinetic (PK/TK) analysis for Preclinical or Clinical studies to Innovative, Generic Pharmaceutical and Biotechnology industry worldwide.

   
 


Sannova’s well qualified scientists, with more than a decade relevant experience in major pharmaceutical corporations, also offer Statistical Services, Data Management and complete Project Management.

Sannova is on the fast track in its expansion and is the fastest growing Bioanalytical CRO in the pharmaceutical industry. 

 
   
 
 
 
Sannova Analytical Inc. is a contract research organization specialized in conducting Bioavailability/Bioequivalence studies for the pharmaceutical industry.

 
 
 

Be the best CRO for providing high quality, cost effective, GXP-compliant bioanalytical services with the highest level of client satisfaction

 
 
     
 
    
Robust Methods for several ther-  
  -apeutic areas.  
Controlled substance methods  
  (CII-CV).  
Preclinical and clinical sample an-  
  -alysis.  
BA/BE studies & PK/TK data ana-  
  -lysis.  
State of the art equipment.  
Reports in eCTD format.  
Access to clinics in USA, Canada&  
  India.  
Complete project management.  
Electronic submission services.  
Strict adherence to GLP.  
Strict security and confidentiality.  
 
 
    
Method Development  
Method Validation  
Pre clinical & clinical sample ana-  
  -lysis.  
Report preparation for bioanalyt-  
  -ical studies reporting.  
Pharmacokinetic & Toxicokinetic  
  Statistics