Fish Health Monitoring Requirements for Cultured Fish Stocks Sample Clauses

Fish Health Monitoring Requirements for Cultured Fish Stocks. The health of each stock of fish reared at a Co-manager or Co-operator facility will be monitored on a monthly basis by a fish health inspector until the fish are released. Any significant loss of fish will be promptly investigated by the facility manager and a fish health inspector. When fish disease agents are detected, preventative and therapeutic strategies will be implemented to reduce the impact of such disease agents on both free-ranging and cultured fish populations. All eggs taken into a culture facility must be water hardened in a minimum of 75 ppm buffered iodophor solution for one hour. However, if the appropriate Co-manager’s or Co-operator’s fish health staff demonstrates that this strategy is detrimental to egg survival for a specific stock, an acceptable alternative will be to disinfect the eggs with 100 ppm iodophor for a minimum of ten
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Fish Health Monitoring Requirements for Cultured Fish Stocks. The health of each stock of fish reared at a Co-Manager or Co-Operator facility will be monitored on a regular basis (target monthly) by a Fish Health Inspector until the fish are released • Any significant loss of fish that is suspected to be due to an infectious agent will be promptly investigated by the facility manager and a Fish Health Inspector. When an infectious agent is detected and implicated in the fish loss, preventative and therapeutic strategies will be implemented whenever possible to reduce the impact of such disease agents on both free-ranging and cultured fish populations

Related to Fish Health Monitoring Requirements for Cultured Fish Stocks

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  • Quality Assurance Requirements There are no special Quality Assurance requirements under this Agreement.

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  • Meteorological Data Reporting Requirement (Applicable to wind generation facilities only)

  • DRUG-FREE WORKPLACE REQUIREMENTS Contractor will comply with the requirements of the Drug-Free Workplace Act of 1990 and will provide a drug-free workplace by taking the following actions: a. Publish a statement notifying employees that unlawful manufacture, distribution, dispensation, possession or use of a controlled substance is prohibited and specifying actions to be taken against employees for violations. b. Establish a Drug-Free Awareness Program to inform employees about: 1) the dangers of drug abuse in the workplace; 2) the person's or organization's policy of maintaining a drug-free workplace; 3) any available counseling, rehabilitation and employee assistance programs; and, 4) penalties that may be imposed upon employees for drug abuse violations. c. Every employee who works on the proposed Agreement will: 1) receive a copy of the company's drug-free workplace policy statement; and, 2) agree to abide by the terms of the company's statement as a condition of employment on the Agreement. Failure to comply with these requirements may result in suspension of payments under the Agreement or termination of the Agreement or both and Contractor may be ineligible for award of any future State agreements if the department determines that any of the following has occurred: the Contractor has made false certification, or violated the certification by failing to carry out the requirements as noted above. (Gov. Code §8350 et seq.)

  • Electronic and Information Resources Accessibility and Security Standards a. Applicability: The following Electronic and Information Resources (“EIR”) requirements apply to the Contract because the Grantee performs services that include EIR that the System Agency's employees are required or permitted to access or members of the public are required or permitted to access. This Section does not apply to incidental uses of EIR in the performance of the Agreement, unless the Parties agree that the EIR will become property of the State of Texas or will be used by HHSC’s clients or recipients after completion of the Agreement. Nothing in this section is intended to prescribe the use of particular designs or technologies or to prevent the use of alternative technologies, provided they result in substantially equivalent or greater access to and use of a Product.

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