Business type
Consultancy, US Designated Representative

Areas of operation
All regions

Company description
Noblitt & Rueland offers specialized consulting expertise in FDA and ISO related issues such as GMP-QSR-QSIT, audits, electronic recordkeeping (Part 11), submissions (510(k)-IDE-PMA-CE mark), design control, risk assessments, hazard analysis, software quality assurance, software compliance audits, independent verification and validation, testing, software development, 483 and warning letter assistance, and extensive in-house training.