Reduce Study Start-up Time…

Study start-up time is critical to the success of a project. Delays starting the project can translate into lost revenue.

PharmaSeek, LLC works with hundreds of independent clinical trial sites throughout the US who participate in clinical trials across a wide variety of therapeutic areas. We can quickly identify and submit high performing, quality sites. We work with the Sponsor or CRO in prequalifying the sites and preparing them for study start-up. Once sites are selected, we will finalize contracts and budgets, prepare and submit regulatory documents to Central IRB, and administer study grants.

We continue to work with the selected sites to manage protocol changes and contract amendments throughout the life of the study.

Making the Connection... Expediting the Process!

PharmaSeek, LLC  •   8301 Excelsior Drive, Suite 113  •   Madison, WI 53717
Contact: Dan Manak, President
T: (608) 662-4177   •   F: (608) 662-4176  •   dmanak@pharmaseek.com

Facilitate Rapid Site Activation And Reduce Costs

• Quickly Identify Qualified, Experienced Investigator Sites

• Coordinate the Completion and Collection of Regulatory Documents

• Complete Site Budgets and Clinical Trial Agreements

• Administer Study Grants

• Free Site Coordinators to Focus on Patient Recruitment

• Provide Single Point of Contact for Multiple Independent Sites

• Enhance Site Performance Throughout the Life of the Study