Reagent Sample Clauses
The REAGENT clause defines the obligations and specifications related to the chemical substances or materials provided or used under the agreement. It typically outlines the quality standards, delivery requirements, and responsibilities for supplying reagents, such as ensuring they meet certain purity levels or are delivered within specified timeframes. This clause ensures that both parties are clear on the expectations for reagents, minimizing disputes over quality or supply and supporting the smooth progress of any processes or experiments dependent on these materials.
Reagent. A chemical compound that is required for the use of the Licensed Material.
Reagent. For exhaust after-treatment systems that use a reagent to reduce emissions, the reagent shall be market reagent and must comply with the specifications of the engine manufacturer. A sample of the reagent shall be taken. The reagent shall not be frozen."
Reagent. Any chemical, biological or immunological components, solutions or preparations intended by the product owner to be used as IVD medical devices.
Reagent. For in vitro diagnostic use only. Phospholipid, calcium chloride, 2–8°C (36–46°F) Unopened – until the expiration magnesium aluminum silicate, date on the pouch label buffers, stabilizers, and or paramagnetic iron oxide particles 20–25°C (68–77°F) Unopened – 2 weeks CAUTION: Exposure of the test cards at any time to magnetic objects or fields (for example, an MRI instrument) can corrupt the encoded information and prevent the analyzer from performing the test.
Reagent. Any chemical, biological or immunological components, solutions or preparations intended by the product owner to be used as IVD medical devices. SELF-TESTING: Testing performed by lay persons. SPECIMEN RECEPTACLE: An IVD medical device, whether vacuum-type or not, specifically intended by their product owner for the primary containment of specimens derived from the human body.