In the American Health Research Network, all seven sites are stream-lined during the study start-up process:

Pharmaceutical sponsors and Clinical Research Organizations should know that we work to minimize negotiations and timelines so that we can move forward with protocol execution. All four sites budgets and contracts are centrally processed at American Health Research. Each site has a quick turn-around time on processing regulatory documents. Each site utilizes a Central IRB which expedites the study-start up process.

We all follow a set of standard operating procedures as well as trial protocols, Good Clinical Practice and HIPAA guidelines to provide a smooth clinical trial process for all involved. Research coordinators are IATA certified and familiar with most electronic data capture systems. All sites make every attempt possible to meet or exceed sponsor contracted enrollment goals. All sites have a large patient database and obtain patient referrals from Investigators’ clinic. All six sites have very dedicated Investigators present at the facility to provide oversight of trial conduct and ensure safe patient care. All sites are experienced conducting Phase II, III and IV trials.

Our sites are equipped with:

• -20 degree freezer

• Secure study drug storage

• Large Patient Database

• On-site lab with ambient centrifuge

• Refrigerator for specimens/drugs

• Hi/Low temperature monitoring for drug room and refrigerator/freezer

• Body Plethysmography

• Lab with CLIA

• Dry ice access

American Health Research has worked with numerous sponsors and CRO's

• Altana

• Amgen

• AstraZeneca

• Avillion

• Boehringer Ingelheim

• Bristol Myers Squibb Pharmeceuticals

• Cephalon

• Cerecor

• Centocor

• Chiltern International

• Daiichi Sankyo

• DEY

• Evidera

• Forest Laboratories

• Glaxo/Smith/Kline

• ICON

• Ikaria

• Kforce