Qualitas Compliance Revenue
Medical Equipment Manufacturing • 
Morrisville, North Carolina, United States • 1-10 Employees
Qualitas Compliance revenue & valuation
| Annual revenue | $427,775 |
| 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 | $1,400,000 |
| Total funding | No funding |
Key Contact at Qualitas Compliance
Sarah Evans
President
Company overview
| Headquarters | Morrisville, North Carolina, United States |
| Phone number | +19199640939 |
| Websites | |
| SIC | 874 |
| Keywords | Medical Device Consulting, ASQ, Medical Device Project Management, Ce Mark Assistance, Fda 21 Cfr Part 820 Compliance Services, Iso 14971 Risk Management Support, Fda Design Controls, Eu Mdr 2017/745, Cqa Lead Auditor Services, Fda 483 Remediation, Fda 510K Submission Support, Iec 60601 Support Services, Iso 13485:2016 Qms Development, Medical Device Certified Safety Testing Support, Medical Device File Review, Medical Device Safety Testing Support, Post Market Surveillance Support, Qms Training For Iso 13485:2016, Unique Device Identification (Udi) Assistance, Fda 21 Cfr Part 820 & Iso 13485:2016 Gap Analysis |
| Founded | 2013 |
| Employees | 1-10 |
| Socials |
Qualitas Compliance Email Formats
Qualitas Compliance uses 1 email format. The most common is {first initial}{last name} (e.g., jdoe@qualitascompliancellc.com), used 100% of the time.
| Format | Example | Percentage |
|---|---|---|
{first initial}{last name} | jdoe@qualitascompliancellc.com | 100% |
About Qualitas Compliance
Qualitas Compliance, LLC is a women-owned business strategically located in Raleigh, NC minutes from the Raleigh Durham Airport and the Research Triangle Park. Qualitas focuses on successfully navigating the ever-changing quality and regulatory waters of the medical device industry. We exist to help our clients move quickly through the compliance aspects of establishing their business along with moving their products through the quality / regulatory paths in preparation for market entry. We understand what it takes to set up a company’s quality system for compliance with ISO 13485:2016, ISO 9001, ISO 14971, GMP, and FDA 21 CFR Part 820 along with compiling FDA ready regulatory submissions to move your product through the compliance channels. Whether you need assistance in writing a single Standard Operating Procedure (SOP), setting up a complete quality management system from scratch, conducting risk management activities, generating a gap analysis, assisting with the Corrective & Preventative process, training, or conducting audits, our knowledgeable and talented team is here to help you achieve compliance!
Employees by Management Level
Total employees: 1-10
Seniority
Employees
Funding Data
Qualitas Compliance has never raised funding before.
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