Medicine transport starts with the product’s own authorised storage information. Do not apply one temperature range to every medicine or one regulatory step to every transport activity.
Match the shipment file
Record product and batch and storage information; consignor, consignee and carrier responsibilities; route and transfer plan; packaging or vehicle choice with qualification evidence for those conditions; logger ID, calibration and shipment temperature profile. At handover, link time, identity and data file.
After an excursion, preserve raw data and segregate the product under the procedure, then notify quality and, where needed, the marketing authorisation holder. Do not decide use, return or destruction from a graph or general regulatory summary alone; obtain a product-specific authorised assessment in writing.
The applicable Turkish text must be confirmed from a current official source for the product, transport activity and parties’ roles. Name the basis and review date in the procedure.