DermPathe has the expertise in taking your topical or transdermal dosage form from in vitro penetration studies to evaluate the safety and efficacy of your drug in vivo in both small and large animal species. DermPathe has the experience of conducting dermal pharmacokinetic studies of topical formulations and transdermal patch systems including active drug delivery systems.

In vivo capabilities include:

 USDA registered and accredited facilities
 More than 25 years of experience in preclinical services partnering with both small and large pharmaceutical and animal health companies.
 Experienced Veterinary and technical staff
 Licensed to handle Scheduled I-V drugs
 All major routes of administration including dermal and transdermal routes
 Surgical capabilities and services in simple as well as complex surgical procedures
 IACUC review services

Once the pharmacokinetic profile is established with in vitro and in vivo models, the safety of your topical or transdermal dosage form has to be established through dermal toxicology studies. DermPathe can provide support to your preclinical toxicology research studies to evaluate dermal toxicology in

 Primary dermal irritation
 Buehler sensitization
 Repeat-dose toxicology

 Acute and chronic exposure studies
 Passive and active drug delivery systems
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Topical & Transdermal Delivery
Pre-formulation & Dosage Form Selection
In Vitro Penetration StudiesSelection
In Vivo Safety & EfficacySelection
Preclinical Model Development
Other Services
Consulting Services
Surgical Services
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                     108, Route 31 South , Washington, New Jersey 07882, USA
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DermPathe Pharmaceuticals
A World class research services provider