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Phase i / bioequivalence
 

Our GCP-compliant custom built 360 bed Phase I clinical unit is at the core of our operations. This 115,000 square foot facility is divided into 6 fully-independent clinics. The facility is also self-sustaining, including onsite kitchen, bi-fuel back-up generator for complete clinical operations, and UPS system. Designed to optimize operational efficiency and provide a comfortable environment for the study participants - we have the ideal infrastructure for clinical research studies.

Combined with our team of medical professionals, extensive SOPs, well developing training programs, and innovative technological systems - PMRI has all the tools to offer you world class services.

We have completed over 1500 studies for submission to regulatory agencies around the world and have extensive experience with various dosage forms including:

Solid oral

Injectables

Oral suspensions

Solutions

Transdermal patches

Creams

Eye drops

Nasal sprays

 

We are also fully licensed for the to run studies with controlled substances.

Special Populations & BE Patient Studies
We recognize that dosing a short panel can have a dramatic impact on the success of your study.
We are proud to let you know that 98% of studies dosed a full panel in 2007. Successful subject recruitment and promoting subject compliance (ambulatory blood draws, etc) are top priorities at Pharma Medica.

Through our extensive recruiting and screening database and network of hospital-based partners,
we are able to run studies in a variety of special population healthy volunteers and patients:

Post-menopausal women
Specific cultural or ethnic groups
Hypogonadal males

Obese patients

Extensive/Poor metabolizers
Oncology patients
Schizophrenic patients

Depressive patients

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