Procedure where Antibiotic Sample Clauses

Procedure where Antibiotic. Milk Contaminates the Tanker Upon arrival at the factory, each milk tanker is sampled and tested for antibiotics. Milk is held on the tanker until the rapid test result is known. In the event of a tanker testing positive on both the rapid and Xxxxx tests, the milk cannot be used and must be dumped. When a milk tanker tests positive to a rapid test, milk collected from each Supplier is then tested using the rapid and Xxxxx to identify the source of the contamination. The tanker is rejected if either the Supplier or Tanker samples test positive to the Xxxxx. Before further milk can be collected from the Supplier identified with the antibiotic milk, a sample must be taken from the vat and test negative to antibiotics. Suppliers will undergo a compulsory internal audit of their procedures to manage antibiotics. The relevant government food authority’s must be notified of all positive consignments and a report submitted by a Norco laboratory technician and a Milk Supply Officer outlining the cause of the incident and the preventative action plan undertaken by the Supplier.
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Related to Procedure where Antibiotic

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  • Studies The clinical, pre-clinical and other studies and tests conducted by or on behalf of or sponsored by the Company or its subsidiaries that are described or referred to in the Registration Statement, the Pricing Disclosure Package and the Prospectus were and, if still pending, are being conducted in accordance in all material respects with all statutes, laws, rules and regulations, as applicable (including, without limitation, those administered by the FDA or by any foreign, federal, state or local governmental or regulatory authority performing functions similar to those performed by the FDA). The descriptions of the results of such studies and tests that are described or referred to in the Registration Statement, the Pricing Disclosure Package and the Prospectus are accurate and complete in all material respects and fairly present the published data derived from such studies and tests, and each of the Company and its subsidiaries has no knowledge of other studies or tests the results of which are materially inconsistent with or otherwise call into question the results described or referred to in the Registration Statement, the Pricing Disclosure Package and the Prospectus. Except as described in the Registration Statement, the Pricing Disclosure Package and the Prospectus, neither the Company nor its subsidiaries has received any notices or other correspondence from the FDA or any other foreign, federal, state or local governmental or regulatory authority performing functions similar to those performed by the FDA with respect to any ongoing clinical or pre-clinical studies or tests requiring the termination or suspension of such studies or tests. For the avoidance of doubt, the Company makes no representation or warranty that the results of any studies, tests or preclinical or clinical trials conducted by or on behalf of the Company will be sufficient to obtain governmental approval from the FDA or any foreign, state or local governmental body exercising comparable authority.

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