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LANDRICH GROUP
QUALITY MANAGEMENT SYSTEMS
Develop Site Audit Plan
Perform Site Audits
Perform Design File and / or Trial Master File Audits
Provide On-going Quality Support
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Attend team meetings
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Advice on quality and regulatory topics
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Attend meetings with partners
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Produce quality and regulatory materials for investor or business development presentations
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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