Capabilities Statement


MAE Group specializes in global regulatory affairs, clinical affairs, project management and  compliance services to medical device, biotechnology and biomedical companies. We assist in the global   commercialization of medical and in vitro diagnostic devices, biologics, pharmaceuticals, cosmetics and  food/beverage products.

Regulatory Affairs
• Strategic Global Regulatory Development
• 510(k), PMA, IDE, IRB submissions
• Feasibility, Pivotal Studies, Program Management
• GLP, GDP and GMP Compliance

Clinical Affairs
• Manage Class II and III Global Multi-Center Device
• Manage Phase I, II, III pharmaceutical studies
• Protocol and Study Documents Development
• Vendor, Clinical Site Contract and Budget Management

Project Management
• Project Management Professional Certified
• Manage $1.6M +multiple and global projects enterprise wide deployment, integration and validation Labware, LIMS Oracle R12, developing middleware
• Manage SDLC global projects passes, resources, budgets

• Approvals in electrical-mechanical systems, disposables, assays in areas including but not limited to cardiovascular, neurology, gastroenterology, radiology, obstetrics/gynecology, orthopedic general and plastic surgery, hematology and immunology

• Pharmaceutical clinical studies include herpes zoster vaccine in oncology, monoclonal antibody dose escalation study, analgesic, CNS, NSAID, anticoagulant, antibiotic, NSAID-induced platelet dysfunction, rare diseases caused by protein deficiencies, enzyme replacement therapy for Fabry disease, and treatments for Hunter syndrome and Gaucher disease, gastrointestinal and surgical oncology, pre-cancerous colon tumors, spinal anesthesia pain management, intravenous pre-op and post-op anti-infective

• Project manage multiple global drug and device clinical studies – drug and device protocol development, multi-site monitoring, vendor contracts, IRB approval, agency approval, informed consent, adjudication meetings, site qualification

Our focused, professional teams provide comprehensive regulatory and clinical expertise to navigate your project from early development thorough final approval. Team members have all of the needed experience and expertise to bring products to global markets. Our small-business agility and flexibility enables unparalleled cost-effectiveness.

MAE Consulting Group LLC
119 North Road, Deerfield, NH 03037
[email protected]
Tel: 603-340-7079

DUNS: 079465752
NAICS CODES: 541990, 541611, 541690, 541711, 541712

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