Pharmaceutical

Acadia Clinical Research team includes one Investigator, two Clinical Research Coordinators, and three Physician Sub-Investigators. Our staff is widely acknowledged as experienced, knowledgeable, detail-oriented, and conscientious in the clinical research field. We pride ourselves on the compassionate and caring demeanor that gives us the ability to provide our participants with outstanding care.

Our experienced personnel are able to:

• Conduct Phase II, III, and IV clinical studies
• Offer time-efficient CRF completion

• Comply with strict study protocols
• Protect the human rights of all study participants
• Comply with all federal guidelines of good clinical practice
• Utilize central IRB for outpatient studies
• Offer timely IRB submission/approval for inpatient studies
• Offer access to centrifuge, ECG machine, dry ice, -20C freezer, secure drug storage areas, secure records retention
• Comply with regulations for maintenance and prompt submission of critical documents
• Offer prompt contract/budget turn-around
• Offer strict GCP adherence
• Comply in full with all HIPAA laws and regulations

Please call (207) 941-9965 for more information and to learn more about Acadia Medical Research.