Are you a start-up medical device company that needs help preparing an FDA 510k submission, quality system, or training?
Medical Device Academy, Inc. is a leading company in medical equipment manufacturing, dedicated to providing comprehensive solutions for regulatory submissions and compliance. Located at 345 Lincoln Hill Rd, Shrewsbury, Vermont 05738, US, Medical Device Academy, Inc. specializes in helping companies navigate the complexities of the medical device industry. With a focus on regulatory submissions such as 510k submissions, CE Marking Technical Files, and Canadian Medical Device License Applications, Medical Device Academy, Inc. ensures that clients meet all necessary requirements.
Medical Device Academy, Inc. also excels in regulatory compliance, offering services like mock FDA inspections, ISO 13485 certification, and CAPA. The company is committed to providing continuing education through webinars and training courses, ensuring that professionals stay up-to-date with the latest industry standards. Medical Device Academy, Inc. has a team that is primarily located in the Eastern Time Zone, with employees across North Carolina, Pennsylvania, New Jersey, Kansas, and Vermont.
Medical Device Academy, Inc. is dedicated to being remarkable and memorable in the industry. The company's commitment to excellence and comprehensive service offerings make it a trusted partner for businesses in the medical device sector. We invite the manager of Medical Device Academy, Inc. to create a customized and exclusive company showcase and product listing on our platform to further enhance its market presence.
Compare Medical Device Academy, Inc. with 1 companies in Medical-Equipment-Manufacturing
| Comparison Field |
Medical Device Academy, I...Main Company |
GMEDView Profile |
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Founded Year
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— | 1994 |
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Company Size
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— | 51-200 |
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City
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Shrewsbury, Vermont | Paris, Ile-de-France |
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Country
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Skills & Keywords
Comparing with main company
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14 Total Skills
Medical Device Manufacturing
Regulatory Submissions
510k Submissions
ISO 13485 Certification
CE Marking
FDA Compliance
Medical Device Licensing
MDSAP Certification
Mock-FDA Inspections
510(k) Submissions
Continuing Education for Regulatory Compliance
De Novo Submissions
Canadian Medical Device Licensing
ISO 13485:2016
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10 Total
10 Unique
Unique Skills:
EU IVDR 2017/746
EU MDR 2017/745
in vitro diagnostics
Innovative technologies
MDSAP
medical device certification
+4
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