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DP Clinical is A ROCK              Accountable: guarantee quality of work              Reliable: high employee retention rate              Offer: proactive suggestions              Committed: to 100% client satisfaction              Knowledgeable: expertise, experience and education
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Services & Capabilities


  • Monitoring
  • Data Management
  • Biostatistics
  • Medical Writing
  • Quality Assurance
  • Regulatory
  • Pharmacovigilance

Biostatistics - DP Clinical is uniquely positioned to support our clients with the services listed below based upon our experience, the thought leadership of our staff, and our technical capabilities.

Biostatistics services include:

● Statistical Consulting
● Clinical trial design
● Protocol development
● Sample size decision
● Statistical analysis plan 
● Statistical programming and validation 
● Devise and validate randomization scheme
● Preparation and review of statistical reports and summaries 
● Interim, exploratory, and meta  analysis
● Preparation of Tables, Listings and Figures 
● Preparation of safety and efficacy summaries 
● Data transfers from vendors, validation and documentation
● Data safety monitoring board (DSMB)

Regulatory assistance services include:

● Regulatory Strategies for Clinical Program
● FDA meetings and presentations
● Annual IND Reports, Drug Master File updates, etc. 

A prospective project team comprising of seasoned biostatisticians, clinical data managers and SAS programmers is assembled to ensure that the key deliverables meet the standards of quality and timeliness that our clients expect and require.  This provides our clients an assurance that they will receive consistent and quality consulting and deliverables throughout the course of the study.  We are proud of our work and committed to quality for each project we undertake.  “Success of each project” is our goal.

 

 

 

 

 

 

 

 

 

 

 

 

 

 


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9201 Corporate Boulevard, Suite 350 | Rockville, MD 20850 | P (301) 294-6226 | F (301) 294-4561 | dpinfo@dpclinical.com