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With 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

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One size does not fit all. This is why Sharp has developed a suite of flexible, scalable and efficient clinical trial management solutions including Clinteract IRT and Clinventory IMS.

Contact us today to schedule a demo: https://lnkd.in/ekUQmFH

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Sharp’s analytical chemists offer a variety of photostability studies for your drug substance or product.

Contact us today to discover how our specialist solutions can improve your #clinicaltrial processes: https://www.sharpservices.com/our-services/clinical/

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