DP Clinical
DP Clinical is a full-service Contract Research Organization (CRO) specializing in dermatology, infectious disease/vaccine, neuroscience, oncology, and ophthalmology clinical programs. Established in 1994 and headquartered in Rockville, MD, DP Clinical provides comprehensive clinical trial services to pharmaceutical, biotech, and medical device companies worldwide. With over 30 years of experience, the company is committed to high standards of quality, data integrity, and client satisfaction, supporting a broad range of therapeutic areas and phases I-III clinical trials.
Industries
Nr. of Employees
large (251-1000)
DP Clinical
Products
Full-service clinical research organization services
Comprehensive clinical trial management services including full complement of clinical trial services or specific functional service offerings.
DP Clinical CRO Services
Full-service contract research organization providing Phase I-III clinical trial services including trial management, monitoring, data management, biostatistics, regulatory affairs, safety monitoring, and medical writing.
Clinical Trial Monitoring Services
Thorough clinical trial monitoring services provided by therapeutically aligned and centrally trained Clinical Research Associates (CRAs) to ensure study integrity, protocol adherence, patient safety, and accurate data collection.
Pharmacovigilance and Safety
Comprehensive pharmacovigilance services for Phase I-III clinical trials, fully compliant with US FDA regulatory standards and ICH E2B Guidelines for Clinical Safety Data Management.
Biostatistics
Comprehensive biostatistics and programming services providing trial design, statistical consulting, programming expertise, and reporting for clinical trials.
Medical Writing
Professional medical writing services adhering strictly to ICH E3 guidelines, delivering clear, concise, and accurate study findings in full compliance with regulatory requirements.
Full-service clinical research organization services
Comprehensive clinical trial management services including full complement of clinical trial services or specific functional service offerings.
DP Clinical CRO Services
Full-service contract research organization providing Phase I-III clinical trial services including trial management, monitoring, data management, biostatistics, regulatory affairs, safety monitoring, and medical writing.
Clinical Trial Monitoring Services
Thorough clinical trial monitoring services provided by therapeutically aligned and centrally trained Clinical Research Associates (CRAs) to ensure study integrity, protocol adherence, patient safety, and accurate data collection.
Pharmacovigilance and Safety
Comprehensive pharmacovigilance services for Phase I-III clinical trials, fully compliant with US FDA regulatory standards and ICH E2B Guidelines for Clinical Safety Data Management.
Biostatistics
Comprehensive biostatistics and programming services providing trial design, statistical consulting, programming expertise, and reporting for clinical trials.
Medical Writing
Professional medical writing services adhering strictly to ICH E3 guidelines, delivering clear, concise, and accurate study findings in full compliance with regulatory requirements.
Services
Program and project-level management for clinical studies across Phase I-III.
On-site and centralized monitoring services to ensure protocol compliance and data quality.
Clinical database setup, EDC management, data cleaning, and preparation of regulatory-ready datasets.
Statistical planning and analysis including sample size/power calculations, SAPs, randomization, interim and final analyses, and statistical programming.
Clinical safety oversight, adverse event review and regulatory safety reporting.
Regulatory strategy, preparation of submissions, and interactions with health authorities.
Program and project-level management for clinical studies across Phase I-III.
On-site and centralized monitoring services to ensure protocol compliance and data quality.
Clinical database setup, EDC management, data cleaning, and preparation of regulatory-ready datasets.
Statistical planning and analysis including sample size/power calculations, SAPs, randomization, interim and final analyses, and statistical programming.
Clinical safety oversight, adverse event review and regulatory safety reporting.
Regulatory strategy, preparation of submissions, and interactions with health authorities.
Expertise Areas
- Clinical trial management
- Biostatistics and statistical programming
- Clinical data management and CDISC standards
- Pharmacovigilance and safety monitoring
Key Technologies
- Electronic data capture (EDC) systems
- Visual data analytics platforms
- Automated KRI monitoring
- CDISC SDTM and ADaM standards
News & Updates
DP Clinical’s Clinical Project Manager Isa McClure was honored with the FASIA Award at the ASIA Conference.
DP Clinical President & CEO Devinder Poonian met with Dr. Nash, the newly elected President of the American Spinal Injury Association.
DP Clinical supports cancer research during May, emphasizing its importance in oncology clinical trials.
DP Clinical honors the professionals making clinical research possible.
Tim Urschel, SVP of RA/QA, attended the SQA annual meeting in Orlando.
The team attended the ASIA scientific meeting in Scottsdale, AZ.
DP Clinical’s Clinical Project Manager Isa McClure was honored with the FASIA Award at the ASIA Conference.
DP Clinical President & CEO Devinder Poonian met with Dr. Nash, the newly elected President of the American Spinal Injury Association.
DP Clinical supports cancer research during May, emphasizing its importance in oncology clinical trials.
DP Clinical honors the professionals making clinical research possible.
Tim Urschel, SVP of RA/QA, attended the SQA annual meeting in Orlando.
The team attended the ASIA scientific meeting in Scottsdale, AZ.