WIL Research Review: Preclinical safety studies

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WIL Research
1407 George Road
Ashland, Ohio 44805-8946
United States
(419) 289-8700
http://wilresearch.com/

Preclinical safety studies

 
Overall: 4 stars

Date: November 28, 2014

Proposal Quality:
 
4
Ease of Contracting Process:
 
4
Comprehensive Solution:
 
3
Experience With Study Type:
 
4
Therapeutic Area Expertise:
 
3
Project Management:
 
3
Responsiveness:
 
4
Problem Solving:
 
3
Adherence to Timelines:
 
3
Adherence to Proposed Budget:
 
3
Reporting Quality / Data Accuracy:
 
3
Value (Price vs Quality):
 
4
Strength as a Partner:
 
4
Willingness to Recommend CRO:
 
4
 

Service Description

To perform various GLP toxicology studies.

What Went Well

CROs can generally accommodate our timeline and find time slots to intiate studies. CRO can gerenally incorporate special needs from the sponsors into the study designs. On the reporting end, CROs generally stick to the timeline in the protocol

What Could Be Improved

CRO could improve on data interpretation and report quality. CROs are not always prompt in addressing client's comments for the reports.

Lessons Learned from the Experience

Under GLP enviroment, CROs are usually conservative and not thinking outside the box. CRO sometimes has certain expertise such reproductive toxicology, phototoxicity, etc., which sponsors can learn from CROs