Our Network
Working with our network of MDs, Ph.Ds and Pharm.Ds, we will assist you with all areas of Protocol Development — from taking your concept to protocol — to adding the finishing touches to the protocol you develop. We can also assist you in all levels of Investigator Drug Brochure (IDB) development. Our Ph.Ds and Pharm.Ds will write your brochure or review the document to ensure it meets all requirements.
Site and Vendor Selection
For Site and Vendor Selection, our experienced monitors have a large network of clinical sites with whom we have worked. We are able to assist you in identifying all types of clinical sites from the most prestigious universities to community level primary care physicians. If you need a central lab, we have experience with every type of laboratory. Or if you need a specialized test, we can find and qualify the lab for you.
Case Report Forms
For many studies, CRA, Inc and our monitors have developed numerous Case Report Forms. We can take your protocol and develop CRFs tailored to your needs. Our network of data management professionals can review your CRFs to ensure all data is being collected to meet your endpoints.
Standard Operating Procedures
Do you need SOPs? We will review your SOPs to ensure they meet all your needs or we can develop all varieties of SOPs for you.
Investigator or Meeting Planning
For Investigator Meeting Planning, we can assist in all stages, from helping you find the best location, to managing the meeting to make your study a success.