planning overview

 Accurate and realistic planning greatly streamlines and facilitates the process of developing medical devices, avoiding costly errors by identifying the key issues and hurdles to be overcome. Periodic review and evaluation at crucial junctures of the development process is not only necessary to avoid delays and product failures, but is mandated by the Design Control requirements. The planning cycle is an essential aspect of all projects as it facilitates coherent and unified processes.

DEQPRO accurately plans and implements:
  • Product development roadmaps with key deliverables & tasks indicated for all major functions & phases
  • Requirements specification, including input from QA/RA and standards
  • Product / process design
  • Risk management
  • V&V testing
  • System integration and testing
  • Studies with Investigational Devices
  • Pilot production

communication tools used:
  • MS Word®, Excel®, PowerPoint®
  • MS Project®
  • Gantt Charts
  • Analyses: FMEA (risk), SWOT, CPM
  • Written and oral communication in English and Spanish
  • Reports tailored to customer’s documentation system requirements