Monitoring - DP Clinical has the capabilities to conduct trials locally, nationally and internationally.  In addition to our headquarters in Rockville, we have ten regional offices located throughout North America, each staffed by trained DP Clinical employees.  We also have affiliates in Central and South America, Europe and India.  Our geographic reach allows us to provide high-quality, cost-effective monitoring for your clinical trials.

Our staff of Clinical Research Associates (CRAs) is highly skilled, holding degrees  as RNs or a BS or MS in a scientific discipline.  Our staff also has diverse language skills including Spanish, French, German, and Hindi/Punjabi.  We also conduct our own rigorous, ongoing in-house training program for all employees.  Our attrition rate for CRAs is less than 10% -- an important consideration given that one of the keys to high-quality clinical trial data is consistency and experience.

DP Clinical has worked in a wide range of therapeutic areas, giving our skilled staff the experience necessary to meet our client’s needs.  We are experienced in managing all aspects of your clinical trial, including:

• Project Management
• Site selection and qualification
• Safety monitoring
• Protocol and informed consent development
  • Design and review clinical study protocols
  • HIPAA Authorizations
• Negotiate and prepare contracts and budgets
• Draft study specific SOPs
• Case Report Form Development and Completion Guidelines
• Conduct investigator meetings
• Monitoring
• Pre-study visits;
• Study initiation visits;
• Interim monitoring visits;
• Study close out visits;
• Monitoring services include 100% source data verification;
• Conduct QA/QC Audits
• Preparation of study reports