Kinesis: CRO in Drug Development and pharmacokinetic

CRO SERVICES FOR PRECLINICAL DRUG DEVELOPMENT

 
Preclinical CRO services
Clinical CRO services
Regulatory CRO services
Population PK/PD modeling
Ghostwriting
Insourcing
 
  o preclinical consultancy.htm
o Study design and protocol writing
o Pharmacokinetic analysis and reporting
o Project management and study monitoring		 o Clinical consultation
o Study design and protocol writing
o Biometrics and report writing
o Project coordination		 o Regulatory affairs consultation
o Regulatory documentation
o Expert reports
o Actualisatie oude dossiers 		Population PK/PD modeling Ghostwriting Insourcing  
               

3. PHARMACOKINETIC ANALYSIS AND REPORTING

Kinesis has extensive experience in the performance of single dose and multiple dose toxicokinetic and pharmacokinetic analyses in support of toxicity studies or e.g. pharmaceutical development, using the WinNonlin software.

All PK or TK-analyses are being performed according to study-specific study plans or protocols and can be performed and reported either under full-GLP or non-GLP with QC-checked reports.

Data analysis results are reported according to our report template or according to a template provided by the sponsor. See also our site about pharmacokinetic support.

 

Address:

Lage Mosten 29
4822 NK Breda
The Netherlands
+31(0)76 54 80 666
+31(0)76 54 21 777 (Fax)

(c) 2003-2004 Kinesis, the Netherlands
info@kinesis-pharma.com