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Advena USA FDA Regulatory ConsultantsHome page for Advena USA FDA Regulatory Affairs Consultants
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Advena USA
Judy Burton
3010 ●●●●●Frwy.
12t●●●oor
Da●●as , Texas, 75234
United States
View this contact
Judy Burton
2653 ●●●●● Lane
Farme●●●●●ranch , Texas, 75234
United States
View this contact
Judy Burton
2653 ●●●●● Lane
Farme●●●●●ranch , Texas, 75234
United States
View this contact
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Advena USA FDA Regulatory Consultants | advenausa.com Reviews
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Home page for Advena USA FDA Regulatory Affairs Consultants
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About Advena USA
http://www.advenausa.com/about.htm
Dedicated to helping medical device companies in registering their. Medical devices throughout the world. Advena USA has over 12 years experience in domestic and foreign regulatory affairs for medical. We have assisted small, medium and large. Foreign and domestic companies in the. Successful completion of their establishment. Registrations, product listings and marketing. Applications in the US, EU, China, Australia,. Brazil, Bahrain, UAE, Turkey, Belgium,. Additionally, our knowledge and experience.
Advena USA FDA Regulatory Consultants
http://www.advenausa.com/index.htm
3010 LBJ Frwy., 12th Floor. Website: www.advenausa.com. Medical Device Regulatory Affairs Consulting. At Advena USA we understand how complex regulatory compliance. Requirements can be. Our experts can assist your company with:. Establishment registration and product listing. FDA 510(k) Pre-market Submissions. International product registration dossiers. Preparation and follow-up to FDA inspections. Responses to recall, deficiency and warning letters. Technical writing and label review.
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Advena USA FDA Regulatory Consultants
3010 LBJ Frwy., 12th Floor. Website: www.advenausa.com. Medical Device Regulatory Affairs Consulting. At Advena USA we understand how complex regulatory compliance. Requirements can be. Our experts can assist your company with:. Establishment registration and product listing. FDA 510(k) Pre-market Submissions. International product registration dossiers. Preparation and follow-up to FDA inspections. Responses to recall, deficiency and warning letters. Technical writing and label review.
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