Calibration Services in Georgia

GlobalMed Logistix (GMLx) is a medical device logistics specialist serving as a critical supply-chain partner for surgical device manufacturers, healthcare providers, and distributors. Operating 150,000+ square feet of FDA-registered facilities, GMLx provides comprehensive logistics and supply-chain solutions across the medical device ecosystem, supporting 1M+ patients annually with 99.9%+ on-time fulfillment rates. Core service offerings include: (1) Inventory Management—cloud-based distribution and inventory management systems with real-time traceability, auditing, reconciliation, and stock/consignment replenishment; (2) Warehousing & Distribution—case management, pick-pack-ship order fulfillment, hospital ordering, distributor consignment replenishment, and national loaner bank operations with after-hours support; (3) Quality Management—FDA Initial Importer and US Agent registration, incoming/outgoing AQL inspections, repackaging and relabeling, instrument tray inspection, and instrument functional testing; (4) Shipping Management—standard and oversized palletization, freight coordination, customized packaging, and domestic/international shipment support; (5) BioSkills Lab—state-of-the-art cadaveric evaluation facility with operating room setting for surgeon training, sales representative engagement, and key opinion leader hands-on education; (6) Quality Control Services—in-process testing, inspections, calibration, final product verification, and process control to ensure device safety, effectiveness, and reliability. The company is FDA-registered and operates under Water Street Healthcare Partners investment backing. GMLx positions itself as the logistics backbone connecting surgical device manufacturers with surgeons and the surgical suite, focusing on the critical workflow between product development, clinical deployment, and patient outcomes.

Mansour Consulting LLC is a specialized regulatory consulting firm serving medical device manufacturers since 2000. Based in Roswell, Georgia, the firm provides comprehensive regulatory solutions spanning FDA 510(k) strategy, ISO 13485 and 21 CFR Part 820 quality systems implementation, UDI/GUDID/EUDAMED compliance, FDA representation (US Agent and Official Correspondent services), technical assistance with R&D and lab testing coordination, and medical device classification/pathway assessment. The firm also develops and markets an integrated compliance software platform combining ERP, document management (DMS), learning management (LMS), labeling, and UDI tools—purpose-built for small to mid-sized medical device manufacturers. With over 30 years of industry experience, the principal provides direct senior-level engagement across the full product lifecycle from pre-market strategy through postmarket surveillance, with regulatory expertise spanning US FDA, EU MDR/IVDR, and Health Canada requirements.