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R&D SUPPORT
Develop verification and Validation Protocols, Plans and Reports​
Support clients with the FDA and other National Competent Authorities communications, regulatory approvals, and inspections​
Manage Analytical and Clinical Validation Studies
Perform Gap Assessments on Design History Files and Technical Files
Prepare regulatory submissions
LANDRICH GROUP
Clinical, Quality, and Regulatory consulting services to Medical Devices, IVD, and Pharmaceutical clients.
CONTACT
2532 Santa Clara Ave Suite 344, Alameda, CA 94501
+1 510 912 2589
@ Since 2017 Landrich Group - All rights reserved.
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