Select a region
North America Europe Asia

[Org_name,1]

[Org_name,1]
About US:
Web Site: [Website,1]
Address:

[Org_addr1,1]
[Org_City,1], [Org_StateProvince,1] [Org_PostalCode,1]
[Org_Country,1]
Phone: [Org_Phone,1]
Fax: [Org_Fax,1]
Email: [Org_Email,1]

Contact:

[Contact1_FullName,1]
[Contact1_Title,1]
[Contact1_Phone,1]
[Contact1_Email,1]

[Contact2_FullName,1]
[Contact2_Title,1]
[Contact2_Phone,1]
[Contact2_Email,1]

Geographic Areas: China
Japan
Australia
Europe
South America
North America
India
Products: Combination Product
Medical Devices
Professional Responsibility (Production): Clinical Trial
Submission/Registrations
Manufacture
Postmarketing
Professional Responsibility (Regulatory Process): Quality System (QS)
Good Clinical Practice (GCP)
Good Manufacturing Practice (GMP)
Premarket Notification (510k)
Registration Establishment
Postmarket Surveillance