global clinical trial returns, reconciliation, and Destruction services
CSM manages returned drug accountability, reconciliation, and destruction for your clinical study; just another reason why working with CSM is refreshingly easy and effective.
Molding our services to meet the exact needs of your clinical study, our capabilities highly surpass those of any other clinical supply service provider. CSM offers GMP and cGMP compliant procedures and processes, and our own highly-trained team will work with each client to meet protocol-specific needs while additionally ensuring the necessary compliance and safety procedures are met.
Our mission at CSM is to professionally and competently manage your clinical supplies through every step of your clinical trial – even if/when changes occur during the process. This means clear and concise communication, especially at the beginning of your clinical study development process. This ensures we are all on the same page in order to mitigate costs, as well as reassure you that we understand that returns can potentially impact the integrity of your study. We are here to make sure that doesn’t happen, but that if it does, we understand the urgency of time.
We recognize your clinical trial team’s initial planning process will inevitably focus on the necessary clinical supplies, clinical trial packaging, and timely delivery of the essential clinical supplies.
The focus is understandably less on later logistics such as the return, reconciliation, and destruction of unused drugs. But by neglecting these action items during the planning process, it can lead to requirement creep and unexpected costs. This is why early dialogue and decisions about returned drug accountability is a crucial, necessary piece of your clinical trial supplies management process.
Choosing the most appropriate system at the start of a clinical study can have a tremendous impact, positively or negatively, on the clinical trial returns process during and at the end of a study. At CSM we value our clients and their successes, and as such, innovation and cost-efficiency is crucial when it comes to accounting for your clinical drug returns, reconciliation, and destruction.
Full Clinical Trial Return, Reconciliation, and Destruction Services:
- Certified Destruction of Hazardous and Non-Hazardous Material through CSM qualified vendors
- Worldwide Returned Drug Accountability and Management
- Physical and Virtual Returns
- Accountability can be completed at the kit level or down to the unit level
- Temperature-Controlled Returns (CRT, Refrigerated, Frozen)
- Return Kits
- Physical or Electronic return kits with materials included for ease of return
- All Services are Available for Controlled Drugs, Schedule II through Schedule V products
- Returns to Inventory
- Certificates of Destruction
LEARN MORE ABOUT RETURN, RECONCILIATION AND DESTRUCTION SERVICES
“I would like to express our sincere thanks to your team for the extraordinary work and dedication. We would not have been able to meet our clinical program goal without CSM’s heroic effort.”
Vice President of Technical Operations, BioPharma Company