

DATA MANAGEMENT
Develop Data Management Plan
Develop Data Edit Specifications
Database Development/Set-up/Programming
eCRF Development and Set-Up
Lead Database Validation Process
Develop CRF Completion Guidelines
Perform EDC User Acceptance Testing and Training
Oversee Database management/hosting and status reports
Provide Additional training session (if required)
Query Generation
Query Resolution
Adverse Event (AE) Coding
Concomitant Medication (ConMed) Coding
SAEs Reconciliation
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Receipt of Vendor Electronic Data (Randomization Center, Central lab, Reading Center, etc... )
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Third-Party Data Reconciliation
Database locking and Report
Data export for Client
Provide On-going Data Management Support
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Attend team meetings
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Advise on data management topics
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Attend meetings with partners
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Produce 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.