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Reducing Inventory Errors in Clinical Trials:
The Impact of Shipment Receipt Verification (SRV) in Vestigo®
Discover how SRV enhances accuracy and reduces inventory correction rates across clinical trial sites.
Investigational Drug Services (IDS) play a crucial role in ensuring patient safety, regulatory compliance, and protocol integrity at clinical research sites. However, inventory errors remain a significant challenge. This whitepaper explores the impact of Shipment Receipt Verification (SRV), a feature in Vestigo®, on reducing inventory errors across clinical trial sites.
Introduced in November 2023, SRV allows for independent verification of shipment receipts, enhancing accuracy and minimizing errors in investigational product (IP) management.
Read the full whitepaper to learn how SRV is transforming inventory management, improving compliance, and supporting better clinical trial outcomes.
About the author
About Rachael Aletti, PharmD
With over 13 years of experience as a licensed pharmacist, Rachael has worked primarily in academic medical centers, starting in inpatient care and transitioning to Investigational Drug Services in 2013. She graduated Summa Cum Laude from Massachusetts College of Pharmacy, completed a PGY1 Pharmacy Practice Residency at Montefiore Medical Center, and practiced at Montefiore before joining the IDS at NYP-Weill Cornell Medical Center.
Rachael joined McCreadie Group in 2019 as an Account Manager, leading new site implementations, optimizing Vestigo at existing sites, and fostering a collaborative community in investigational drug services. She pioneered the growth of the Research Pharmacy Summit and Vestigo’s Customer Success team before transitioning to Business Development Manager, focusing on new contracts and strategic planning. Now a Solutions Engineer, Rachael combines her technical expertise with deep knowledge of research pharmacy management to understand client needs and showcase Vestigo’s capabilities.