Analytical Laboratory Data Management Sample Clauses

Analytical Laboratory Data Management. The analytical laboratories utilize several standardized data reporting tools developed specifically for the ▇▇▇▇▇ project to ensure consistency between laboratories in the presentation and submittal of analytical data. In general, a unique ▇▇▇▇▇-specific EDD has been developed for each analytical method and each sampling medium. Electronic copies of all current EDD templates are provided in the ▇▇▇▇▇ Lab eRoom. Once the analytical laboratory has populated the EDD with results, the spreadsheet(s) are transmitted via email to the ESAT TEM Laboratory Manager, the ESAT project data manager, and the FTL (or their designee). (Other email recipients may also be specified by the ESAT LC). The ESAT project database manager utilizes a local analytical Scribe project database (i.e., LibbyLab2012.mdb) to maintain analytical results information. The ▇▇▇▇ are uploaded directly into the analytical Scribe project database. It is the responsibility of the ESAT project data manager to publish analytical results information from the local analytical Scribe database to ▇▇▇▇▇▇.▇▇▇.

Related to Analytical Laboratory Data Management

  • Laboratory Testing All laboratories selected by UPS Freight for analyzing Controlled Substances Testing will be HHS certified.

  • Manufacturing (a) The Supplier shall without limitation be responsible, at no additional cost to the Purchaser, for: sourcing and procuring all raw materials for the Products; obtaining all necessary approvals, permits and licenses for the manufacturing of the Products; providing sufficient qualified staff and workers to perform the obligations under this Purchase Agreement; implementing and maintaining effective inventory and production control procedures with respect to the Products; and handling other matters as reasonably requested by the Purchaser from time to time. (b) The Supplier shall not change any process, material, component, packaging or manufacturing location without the Purchaser’s express prior written approval.

  • Laboratory a. Drug tests shall be conducted by laboratories licensed and approved by SAMSHA which comply with the American Occupational Medical Association (AOMA) ethical standards. Upon advance notice, the parties retain the right to inspect the laboratory to determine conformity with the standards described in this policy. The laboratory will only test for drugs identified in this policy. The City shall bear the cost of all required testing unless otherwise specified herein. b. Tests for all controlled substances, except alcohol, shall be by oral fluid testing and shall consist of two procedures, a screen test and, if that is positive, a confirmation test. c. To be considered positive for reporting by the laboratory to the City, both samples must be tested separately in separate batches and must also show positive results on the confirmatory test. d. In the event of a positive test, the testing laboratory will perform an automatic confirmation test on the original specimen at no cost to the Covered Employee. In addition, the testing laboratory shall preserve a sufficient specimen to permit an independent re-testing at the Covered Employee’s request and expense. The same, or any other, approved laboratory may conduct re-tests. The laboratory shall endeavor to notify the designated MRO of positive drug, alcohol, or adulterant tests results within five (5) working days after receipt of the specimen.

  • Random Drug Testing All employees covered by this Agreement shall be subject to random drug testing in accordance with Appendix D.

  • Supplier Development lf the Buyer identifies problems in supplier performance based on supplier monitoring, he shall initiate improvement measures at the Supplier. The Buyer shall pursue the possibilities of continuous improvement of the Supplier. The supplier audit is a form of supplier development; the exchange of information and experience between the Buyer and the Supplier also serves this purpose.