Maintenance & Repair in New Hampshire

HiArc is a medical device engineering and manufacturing company specializing in design, engineering, and manufacturing services for diagnostics and life sciences companies. Founded in 1980 and based in Merrimack, New Hampshire, the company employs 200–500 people and operates as a strategic partner across the full product lifecycle—from concept development and engineering design through manufacturing and ongoing support. HiArc brings deep expertise in laboratory automation, robotics, precision engineering, microfluidics, thermal control, optics, and motion control. The company serves startups and global original equipment manufacturers in the diagnostics, biotech, and medtech sectors, with over 40 years of partnership experience. HiArc emphasizes collaborative, quality-driven processes that align with client goals and deliver regulatory-compliant, real-world-ready solutions.

Makromed, Inc. is a quality management system (QMS) software and regulatory affairs (RA) consulting firm serving the medical device, diagnostic, pharmaceutical, nutraceutical, and biotechnology industries. The company offers a comprehensive suite of cloud-based QMS software modules including InfoPV (Process/Test Method Validation), InfoSQA (Software Validation), InfoMed (Complaints/Adverse Events Management), InfoCAPA (Corrective/Preventive Actions), InfoAudit (Internal and Supplier Audits), and InfoTrain (Employee Training). In addition to software, Makromed provides specialized consulting services in process and test method validation, software validation, risk management, statistical techniques and biostatistics, design controls, CAPA implementation, Six Sigma tools, and regulatory compliance auditing. The firm also offers FDA-focused training through MyFDAcademy.com, an interactive online platform covering QMS and RA topics. With ISO 13485:2016 certification, Makromed serves as a trusted partner for companies navigating FDA QSR, MDR, and ISO 13485 requirements, including 510(k) and De Novo submission support for software-driven medical devices. The company's expertise spans design control, reliability analysis, and regulatory strategy for medical device manufacturers and service providers.

Fuhrmann GmbH is a German medical device manufacturer and distributor specializing in sterile consumables, disposables, and surgical instrument sets for hospitals, medical practices, outpatient surgery centers, and care facilities. The company manufactures and supplies wound care dressings (Verbandstoffe), custom sterile operative and care sets (OP- & Pflege-Sets branded as MEINSET), single-use sterile instruments (Einmalinstrumente), and sterile single-use bowls (Sterile Schalen). Fuhrmann operates as an owner-managed mid-size enterprise with production facilities in Germany and Czech Republic, emphasizing supply chain resilience and high hygiene standards. The company offers contract manufacturing and packaging services (Lohnverpackung) for medtech companies, handling demanding regulatory and production processes. Certified for MDR compliance and quality management, Fuhrmann serves clinics, group purchasing organizations, medical practices, and multi-specialist centers (MVZ). The company emphasizes rapid delivery, flexible customization, and reliable supply security through European manufacturing infrastructure.