Common use of Distribution Records Clause in Contracts

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 or upon request, within two working days, by sending a fax, confirmed by a letter, to: ViraNative AB Viragen (Scotland) LTD. Tvistevagen 48 Pentland Science Park S-907 30 Xxxx Xxxx Xxxx, Peniculk Sweden Mxxxxxxxxx XX000 XXX Xxxxxx Xxxxxxx Tel no: 40-00-000000 Tel no: 40-000-000-0000 Fax no: 40-00-000000 Fax no: 40-000-000-0000

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 or upon request, within two working days, by sending a fax, confirmed by a letter, to: ViraNative AB Viragen (Scotland) LTD. Tvistevagen 48 Pentland Science Park S-907 30 00 Xxxx Xxxx Xxxx, Peniculk Sweden Mxxxxxxxxx Xxxxxxxxxx XX000 XXX Xxxxxx Xxxxxxx Tel no: 4000-00-000000 Tel no: 4000-000-000-0000 Fax no: 4000-00-000000 Fax no: 4000-000-000-0000

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 or upon request, within two working days, by sending a fax, confirmed by a letter, to: ViraNative AB Viragen (Scotland) LTD. Tvistevagen Tvistevägen 48 Pentland Science Park S-907 30 36 Umeå Xxxx Xxxx XxxxLoan, Peniculk Penicuik Sweden Mxxxxxxxxx Xxxxxxxxxx XX000 XXX Xxxxxx Xxxxxxx Tel no: 4000-00-000000 Tel no: 4000-000-000-0000 Fax no: 40. 00-00-000000 Fax no: 4000-000-000-00000000 License Agreement - Arriani Pharmaceuticals, S.A. Date: May 21, 2003 5 of 22

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 or upon request, within two working days, by sending a fax, confirmed by a letter, to: ViraNative AB Viragen (Scotland) LTD. Tvistevagen Tvistevägen 48 Pentland Science Park S-907 30 36 Umeå Xxxx Xxxx XxxxLoan, Peniculk Penicuik Sweden Mxxxxxxxxx Xxxxxxxxxx XX000 XXX Xxxxxx Xxxxxxx Tel no: 4000-00-000000 Tel no: 4000-000-000-0000 Fax no: 40. 00-00-000000 Fax no: 4000-000-000-00000000 License Agreement - Arriani Pharmaceuticals, S.A. Date: May 21, 2003