


QA Sight - Quality Assurance and Regulatory Affairs for medical devices Revenue
Medical Equipment Manufacturing • Hadera, Haifa District, Israel • 1-10 Employees
QA Sight - Quality Assurance and Regulatory Affairs for medical devices revenue & valuation
| Annual revenue | $85,555 |
| Revenue per employee | $86,000 |
| Estimated valuation?This valuation is estimated based on industry average for the Medical Equipment Manufacturing industry and current estimated revenues | $273,776 |
| Total funding | No funding |
Key Contact at QA Sight - Quality Assurance and Regulatory Affairs for medical devices
Sasha Gelfand
Founder
Company overview
| Headquarters | Hadera, Haifa District, Israel |
| Website | |
| NAICS | 3391 |
| Keywords | Risk Management Implementation, Biocompatibility Strategy & Documentation, Clinical And Technical Team Support, Design History File (Dhf) Management, Early Development Regulatory Strategy, Fda Regulatory Submission Support, Iso/Iec 27001 Auditing & Gap Assessment, Labeling & Ifu Compliance, Medical Software Regulatory Support, Post-Market Surveillance (Pms) Documentation, Product Safety Standards Support, Regulatory Documentation Development, Sterilization Validation & Regulatory Support |
| Employees | 1-10 |
About QA Sight - Quality Assurance and Regulatory Affairs for medical devices
QA Sight was founded on a clear mission: to transform regulatory complexity into actionable clarity—empowering medical device companies to bring safe, effective, and compliant products to market with confidence. Led by a seasoned industry expert with over 20 years of hands-on experience, QA Sight was created to bridge the critical gap between engineering innovation and regulatory expectations. We understand that success in this industry depends not just on meeting requirements, but on integrating them seamlessly into your product lifecycle. From early-stage startups to multinational manufacturers, we’ve guided clients through the evolving landscape of global regulations—turning uncertainty into strategic advantage. Our approach is pragmatic, audit-ready, and tailored to your product’s risk, technology, and market goals. Whether you’re navigating FDA pathways, aligning with EU MDR, implementing ISO 13485 systems, or designing a risk management file that truly reflects real-world use—QA Sight is more than a consulting service. We are your strategic compliance partner, ensuring that quality is built in—not bolted on.
Employees by Management Level
Total employees: 1-10
Seniority
Employees
Employees by Department
QA Sight - Quality Assurance and Regulatory Affairs for medical devices has 1 employees across 1 departments.
Departments
Number of employees
Funding Data
QA Sight - Quality Assurance and Regulatory Affairs for medical devices has never raised funding before.
Frequently asked questions
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