pddetrials - a web-based clinical data solution

Pacific Data Designs, LLC and ClinPro, Inc. are now ClinOps, LLC.

Why ClinOps, LLC?

Expertise. Speed. Responsiveness. Reliability.

ClinOps, LLC is a focused contract research organization serving the Biotechnology, Pharmaceutical and Medical Device industries. ClinOps mission is to be a trusted partner to our clients by utilizing our deep expertise in data management, SAS/statistical services and Investigator-initiated study management to deliver superior quality projects within aggressive timelines.

Our Core Services


Clinical Data Management:

ClinOps offers a comprehensive suite of Data Management services including:

  • Case Report Form (CRF) Design for virtually all therapeutic areas
  • Database Design & Development
  • Data Capture
  • Quality Control (Discrepancy Management/Query Resolution)
  • Customized Reporting Features
  • SAE Management
  • MedDRA & WHODrug Coding
  • External Data Import (Data Loads)
  • Imaging & Documentation Center


Statistics and SAS Programming Services:

Our experienced Ph.D. and M.S.-level staff provide the following services:

  • Protocol Review and Input
  • Sample Size Calculation and Justification
  • Randomization Schedules
  • Statistical Analysis Plan Preparation and Review
  • Table, Listing and Figure Programming and Validation
  • Patient Profile and Physician Report Programming
  • DSMB Report Preparation and Meeting Participation
  • Interim Analysis Planning and Conduct
  • Clinical Study Report Input and Review
  • Ad Hoc Statistical Analysis
  • CDISC SDTM and ADaM Domain Preparation and Submission Documentation
  • FDA/Advisory Panel Meeting Planning and Participation
  • Publication Support

Investigator-Initiated/Study Management:

With over 30 years of experience in clinical data management, ClinOps has made it our goal to help clients advance and accelerate therapeutic clinical drug and device development initiatives by participating in investigator-initiated trials. We provide a single, consistent point of contact to advise and ensure that not only is the necessary data being closely monitored and cleaned, but that all regulatory documentation is in place and that the post-study analysis is submission-ready.


Our Technology:

ClinOps offers two distinctive Data Management applications to give its clients a wider range of flexibility in features and style. Both applications have been extensively validated to ensure efficiency, intuitive navigation and 21 CFR Part 11 compliance.

pddEtrials®:

pddEtrials® is a proprietary clinical trials management system that provides the most intuitive, advanced, flexible, and customizable data capture solution. Utilized by both ClinOps employees and our clients through a web based application, this SQL based system is designed by site monitors and sponsors to be a user friendly and adaptable system. Whether you prefer electronic or paper-based data capture methods, pddEtrials® offers deep visibility and fast access allow each group to stay in touch with their data - anywhere, anytime.

ClinPlus®:

ClinPlus Data Management (CPDM) is a robust Data Management software employed by over 50 Biotechnology, Pharmaceutical and Medical Device companies. CPDM software has been engineered to achieve highly efficient clinical trial data processing with a minimal investment in installation and setup. CPDM is a comprehensive SAS-based system that is flexible enough to support a vast range of scenarios, yet fully customizable to meet each organization’s specific requirements.