Returns, Reconciliation, and Destruction
Sponsors and investigators must maintain 100% accountability for all experimental medicinal items used in clinical studies, according to federal rules. This entails keeping track of the drug’s disposition, amounts, usage or unused status, and actively managing completed and / or abandoned clinical sites.
Why Choose Patwell?
Getting study medications packaged, distributed, and given to your first patient is frequently the main goal of the beginning of a clinical study. Although this focus makes sense, closing down your clinical trial and dealing with responsibility, reconciling returns, and destroying both used and unused medication products can be difficult and ignored.
To assist your clinical study to come to an end, Patwell provides thorough returns reconciliation and destruction services. Our staff will collaborate closely with you to create a suitable reconciliation plan that adheres to your clinical procedure while upholding safety and regulatory standards. Patwell’s skilled professionals will complete your reconciliation in accordance with GMPs, whether you require a straightforward receipt and keep until destruction or disassembling each kit and counting each individual tablet.
Patwell may also assist you in properly disposing of your pharmaceutical products after your study is over. Patwell offers comprehensive records of the receipt and handling of returns. A qualified and licensed facility completes destruction in accordance with customer criteria.
Contact Patwell
See our full suite of services below.
Logistical Services
Project Management
Packaging and Labeling
Returns, Reconciliation, and Destruction
GMP Storage