Distribution Records. In order to enable the Company to comply with the requirements of the European Code of Good Manufacturing Practice (Volume IV of the Rules Governing Medical Products in the European Community), the Distributor shall keep Distribution Records for each Batch of the Product sold to the customers. This information shall be made available to the Company in case of Recall Operation, within two working days, by sending a fax, confirmed by a letter, to: ViraNative AB T▇▇▇▇▇▇▇▇▇▇ ▇▇ ▇-▇▇▇ ▇▇ ▇▇▇▇ ▇▇▇▇▇▇ Tel no: 4▇-▇▇-▇▇▇▇▇▇ Fax no: 4▇-▇▇-▇▇▇▇▇▇
Appears in 1 contract
Sources: Supply and Distribution Agreement (Viragen International Inc)
Distribution Records. In order to enable the Company to comply with the requirements of the European Code of Good Manufacturing Practice (Volume IV of the Rules Governing Medical Products in the European Community), the Distributor shall keep Distribution Records for each Batch of the Product sold to the customers. This information shall be made available to the Company in case of Recall Operation, within two working days, by sending a fax, confirmed by a letter, to: ViraNative AB T▇▇▇▇▇▇▇▇▇▇▇ ▇▇ ▇-▇▇▇ ▇▇ ▇▇▇▇ ▇▇▇▇▇▇ Tel no: 4▇▇-▇▇-▇▇▇▇▇▇ Fax no: 4▇▇-▇▇-▇▇▇▇▇▇
Appears in 1 contract
Sources: Distribution Agreement