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Non-Product Software Validation



Non-Product Software Validation


ADB Automation and Validation Group offers our experience in the establishment and execution of non-product software validation processes to support Medical Device and Pharmaceutical Companies, among other sectors. To this end, we possess knowledge and experience in the following areas:


  • Meeting FDA product development and manufacturing regulations for diagnostic, implantable, Class I, II, III medical devices, Biologics, and meeting related industry regulations such as AAMI, AIMD, ICH, MDD, ISO, CFR and IEC.
  • Maintaining documentation revision control using object oriented control systems including Documentum®, Agile PLM®, SharePoint®, Scripts, and Master Control.
  • Supporting quality assurance processes, corrective and preventative actions, complaints, issues, field service, non-conformance, supplier, receiving inspection, and device accountability, Packaging and Transportation, product traceability, return goods systems, manufacturing, audits, and training systems.
  • Adhering to FDA warning mitigations, including FDA 21 CFR Part 11, FDA 21 CFR Part 211, 49 CFR and FDA 21 CFR Part 820.
  • Supporting manufacturing and logistics systems, such as those that involve SAP, PeopleSoft, Microsoft Dynamics, and QAD.
  • Running clinical database systems such as Oracle Clinical, ClinTrials, MetaData, SAS, RDC, DataFax, image management systems, labs management systems, adverse event management systems, coding management systems, thesaurus management systems, MEDDRA, WHODRUG, WHOART, clinical study management, and trial management.
  • Incorporating System development life cycle assessment comprising concepts, design, implementation, installation, integration, and maintenance.
  • Standardizing operating procedure and qualification protocol development.
  • Validating reports for packaging lines, Assembly, Automated Testing Systems, manufacturing Systems, End of Line Testers, reliability Systems, and In-process Systems.
  • Implementing documentation testing and evaluation standards pursuant to IEEE, FDA & ISO standards, such as ISO 13485.




Testimonial / What Our Client Say

Andre and his team were professional, focused and sensitive to the timing issues associated with my project. Most importantly, after the project completed Andre and his team did not disappear. As I needed answers and follow up information, his team followed up in a timely and accurate manner. I look forward to using the services again and would recommend them highly.

Erik Emerson, President & CEO at Symplmed

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