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DP Clinical, Inc.

9201 Corporate Boulevard, Suite # 350
Rockville, MD 20850, USA

Category: Clinical Trials Services (CRO); R&D Services

Used in the following map:

Maryland Biotech Industry Map

DP Clinical, Inc. is a contract research organization (CRO) that serves pharmaceutical and biotechnology clients by providing Project Management, Monitoring, Data Management, Biostatistics and data analysis, and Medical Writing services for Phase I - IV clinical trials. It was established in 1994, with a goal to provide the highest quality of clinical and data management services to the life sciences industry and to satisfy its clients.

DP Clinical is focused on the following therapeutic areas that include: neurological disorders, pediatric trials, cardiology, infectious diseases, ophthalmology, HIV/AIDS, respiratory, oncology, rheumatology, blood disorders, etc. It offers a wide range of clinical trial services that include: project management, site selection and feasibility questionnaire, safety monitoring, preparation of study specific SOPs, monitoring, etc. The company provides an extensive array of clinical data management services that include: design of case report form or eCRF, preparation of CRF or RDC guidelines, data coding using MedDRA and WHO Drug, preparation of data management plan, design database, query management, etc. Its biostatistics services are - clinical trial design, development of statistical analysis plan, statistical programming and validation, interim , exploratory, and meta analysis, data transfers from vendors, validation and documentation, etc.

DP Clinical provides a wide range of medical writing services. The company's medical documents that it normally works on includes: standard operating procedures (SOPs), summary of clinical safety/ISS, integrated summary of efficacy (ISE) reports, serious adverse events (SAE) narratives, etc. Its range of regulatory services include: preparation of recruitment and subject information materials, preparation of informed consent form, review and maintenance of documentation and records, review of advertising and promotional materials, technical writing including clinical study reports and investigator's brochures, etc. The company is also engaged in offering quality assurance and pharmacovigilance services.