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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.

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CONTACT

2532 Santa Clara Ave Suite 344, Alameda, CA 94501

+1 510 912 2589

@ Since 2017 Landrich Group - All rights reserved.

Contact us

For any questions you have, you can reach us here:

Tina Landess

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2532 Santa Clara Ave, Suite 344

Alameda, CA 94501

United States

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admin@landrichgroup.com

+1 510.912.2589

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© 2025 by Landrich Group 

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