The physicians and staff of Investigative Clinical Research work closely together on each trial to ensure its success. We understand that many factors go into the timely, accurate and safe completion of a pharmaceutical trial and we continually strive to meet a sponsors needs.
- Wireless DSL
- On site storage of all documents
- Designated monitoring space
- Protocol specific source documents
- Low query rates with rapid resolution
- Central IRB
- Timely enrollment with goals met
- Centrally located; within driving distance of other metro areas
- Very close to Baltimore Washington International Airport
To generate clean reliable data that can withstand the toughest FDA scrutiny is our key priority. So meeting or exceeding recruitment targets is important, but only if the data is of the highest possible quality.