Keeping it Moving – The Fundamentals of Clinical Supply Import/ Export
The globalisation of clinical trials is on the rise now more than ever. Global Clinical logistics requirements and Importer Of Record (IOR) responsibilities are some of the concerns for companies operating within the pharmaceutical and biotech industry.
Our Subject Matter Expert, Sharon Courtney, Logistics Service Manager, shares her expertise related to:
- Importer of Record (IOR) responsibilities
- Product Valuation Methodology
- Requirements for Logistics Providers
- Customs and Customs Broker Interactions
- Temperature Controlled Shipping Solutions
Sharon is an International Logistics Specialist having worked for 18 years in Clinical Supply Chain. She has expert knowledge in a number of key areas within the end to end supply chain process including management and control of temperature sensitive shipments; risk mitigation (identifying and managing risk); developing and managing robust relationships with transport partners; chain of custody responsibilities; active and passive shipping solutions and import and export country knowledge.
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Almac Clinical Services
Guided by our extensive clinical supply experience and expertise, Almac Clinical Services is recognised as an innovative, global solution provider within the specialised and complex market of clinical trial supply.
Our integrated and adaptable solutions offer the most flexible approach to support the delivery of global clinical trials from protocol right through to patient delivery.
Our core purpose is to be the partner of choice, to deliver the next generation of health care solutions effectively and to focus on winning for you and your patients.