IN PARTNERSHIP
caused by customs inspections and temperature VAT) that apply when importing comparator material from other markets must be assessed
It’s common for material sourced from a different market to have a different language and a different set of information than what is required in the market where patients are required by local regulatory authorities needs
need to be translated into the local language? Should the label be translated into the market the material is sourced from or in the target market? If additional labelling activities are •
• What is the time required to perform
Even selecting a new or additional
packaging/labelling provider needs to be considered and can further impact timelines
on your clinical trial – even patients or patient
engagement can be impacted when you face a drug shortage situation without Identifying potential risks when building a sourcing strategy will allow you to develop a and keep patients engaged in the clinical trial. Thinking at an early stage about those
with your selected sourcing partner early will enable you to build a robust and flexible
CSI: the science-based leader in clinical supported clients in similar situations and have the knowledge and experience to support you in identifying the risks and back-up options to be prepared for drug shortages and developing
route to improve the speed and agility of your study. We leverage our global network of over 95 manufacturers in emerging markets to source high-quality comparator drugs and
For more information on how we identify
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