Storage of the Investigational Product Skladování Hodnoceného léčiva Sample Clauses

Storage of the Investigational Product Skladování Hodnoceného léčiva. The Institution shall ensure that the Investigator shall store all Investigational Products securely as designated in the Protocol, but in any event, in either a central pharmacy where a qualified pharmacist supervises dispensing or in a restricted area and dispensed under the direct supervision of the Investigator. Zdravotnické zařízení zajistí, že zkoušející bude všechna hodnocená léčiva skladovat bezpečně, jak je stanoveno v protokolu, v každém případě však buď v hlavní lékárně, kde dohlíží na výdej kvalifikovaný lékárník, nebo v místě s omezeným přístupem, a hodnocená léčiva budou vydávána pod přímým dohledem zkoušejícího.
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  • Packaging Materials and Containers for Retail Sale Packaging materials and containers in which a good is packaged for retail sale shall, if classified with the good, be disregarded in determining whether all the non-originating materials used in the production of the good undergo the applicable change in tariff classification set out in Annex 4, and, if the good is subject to a regional value-content requirement, the value of such packaging materials and containers shall be taken into account as originating or non-originating materials, as the case may be, in calculating the regional value content of the good.

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  • Investigational Services This plan covers certain experimental or investigational services as described in this section. Clinical Trials This plan covers clinical trials as required under R.I. General Law § 27-20-60. An approved clinical trial is a phase I, phase II, phase III, or phase IV clinical trial that is being performed to prevent, detect or treat cancer or a life-threatening disease or condition. In order to qualify, the clinical trial must be: • federally funded; • conducted under an investigational new drug application reviewed by the Food and Drug Administration (FDA); or • a drug trial that is exempt from having such an investigational new drug application. To qualify to participate in a clinical trial: • you must be determined to be eligible, according to the trial protocol; • a network provider must have concluded that your participation would be appropriate; and • medical and scientific information must have been provided establishing that your participation in the clinical trial would be appropriate. If a network provider is participating in a clinical trial, and the trial is being conducted in the state in which you reside, you may be required to participate in the trial through the network provider. Coverage under this plan includes routine patient costs for covered healthcare services furnished in connection with participation in a clinical trial. The amount you pay is based on the type of service you receive. Coverage for clinical trials does not include: • the investigational item, device, or service itself; • items or services provided solely to satisfy data collection and that are not used in the direct clinical management; or • a service that is clearly inconsistent with widely accepted standards of care.

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