DP Clinical, Inc.

Services & Capabilities

Monitoring - DP Clinical has the capabilities to conduct trials locally, nationally and internationally. In addition to our headquarters in Rockville, we have regional offices located throughout US, each staffed by trained DP Clinical employees. We also have affiliates in South America, Europe, South Africa 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 feasibility questionnaire
●	Safety monitoring
	º	Informed consent development
●	Preparing recruitment materials and subject information pamphlets
●	Site and vendor contracts and budgets
●	Prepare study specific SOPs
●	Conduct investigator meetings
●	Monitoring
	º	Site Qualification visits;
	º	Study initiation visits;
	º	Interim monitoring visits;
	º	Study close out visits;
	º	Monitoring services include 100% source data verification all variables;
●	Provide GCP training to sites
●	DPCTrack to track study status and documents

DPC also has a secure web portal which allows clients to review their documents (e.g. regulatory documents, reports, subject status, investigator payment status) on line.