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Returns and destructionWith pressure to get products to market and meet corporate targets, it’s understandable that the returns and destruction elements of clinical trials are often something of an afterthought.

At Sharp, we proactively encourage our clients to plan ahead and create an outline plan for how returns, reconciliation and destruction will be managed during the set-up phase of the project. It’s the best way to make sure the process is handled as efficiently and cost-effectively as possible.

Our experts can help you plan ahead, so when your trial comes to an end you can focus on moving forward, knowing it’s all is taken care of. If you’re there already and need some extra support now, we also have well-established procedures that can be rolled out to any study at short notice.

Our services include:

  • Customer and project-specific returns and reconciliation protocols
  • Ample, dedicated returns storage
  • Regulatory compliance and documentation support
  • Reconciliation services
  • Hazardous and non-hazardous destruction
  • Updated and complete documentation on destruction
  • Issuing of certificates of destruction

Related Resources

Great to meet new and familiar faces at #CTSBoston2019 this week!
If you missed our round table discussion on how to leverage #ClinicalIRT to improve #clinicaltrial efficiency, you can watch our on-demand webinar here: https://t.co/oHjmki0sPi
@proventaintl

#CTSBoston2019 has officially come to an end! Thank you to all our sponsors and partners for supporting us in this educational day of executive networking and building strategic partnerships! Hope to see you all again in our next CTS Strategy Meeting. https://t.co/KbkDfwYIRB

#Webinar | Are you paying too much tax on your #clinicalsupply shipments? Join Sharp for a live webinar in discussing how you can optimise your #clinicaltrial supply shipments into & out of the UK, from both non-EU and EU locations.
Click to register: https://t.co/o2P1Qlwx9E