Camargo Preclinical Service

Camargo ensures the appropriate regulatory requirements are met every step of the way, streamlining your drug development process all the way to approval.

Ready to guide you through the preclinical stage of drug development, Camargo provides strategic support in the following areas:

• CRO selection
• Study design
• Study setup and execution
• Project management

In clinical program development, camargo's focus is unwavering: Move products from preclinical through to FDA approval as efficiently as possible. Using proven methodologies that can meet FDA guidance requirements and expedite the drug approval process while reducing overall study costs.

Experts develop a customized clinical program plan for each drug, which includes only the services necessary for preparation and hands-on implementation.

Also seasoned medical writers apply their proven research and investigation skills to design protocols that streamline the clinical trial process, reduce study costs and expedite the drug approval process. When protocol design is complete, Camargo's team moves from planning to implementation, all the while working in close partnership with your team.


Camargo Clinical Design Expertise:

• Bioavailability
• Bioequivalence
• Comparison
• Dose-ranging
• Drug interaction
• Drug metabolism
• Efficacy
• Patient preference
• Proof-of-concept
• Quality of life
• Radiopharmacology
• Safety