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  
               

2. PRECLINICAL STUDY DESIGN AND PROTOCOL WRITING

Kinesis has extensive knowledge about and experience in the design of non-clinical studies in all fields of studies needed for regulatory submission (hyperlink naar www.kinesis-pharma.com). Kinesis works together with a vast number of preclinical CROs for conducting the practical work of pre-clinical studies.

In practice Kinesis informs these contracts labs on the intended study design. The labs write the protocols according to their own standards and Kinesis reviews these study plans. Study plans for pharmacokinetic and toxicokinetic evaluation are being written in-house (see pharmacokinetic analysis and reporting). See also our site about drugdevelopment.

 

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