Other Medical Device or Medication Specified for Use During the Study Sample Clauses

Other Medical Device or Medication Specified for Use During the Study. No other medical devices or medications are required to be used in conjunction with the treatments during the clinical study.
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Other Medical Device or Medication Specified for Use During the Study. During the clinical study, the following additional medical devices are required: • Habitual optimized lenses will be optimized for power o Contact lenses will not be over labeled (subjects know they are wearing their habitual lenses) o Subjects will be instructed by site personnel to use their habitual lenses according to the instructions for use o Subjects will be provided with 1 to 10 habitual optimized lenses per eye, depending on replacement schedule o Subjects will be instructed to wear lenses each day for at least 8 hours per day over the study treatment duration (7±2 days) o Subjects will continue to use their habitual lens care products when wearing the optimized habitual lenses
Other Medical Device or Medication Specified for Use During the Study. Other than the pre-specified CLEAR CARE, LacriPure (or equivalent), and Systane rewetting drops, no other ocular medical devices or medications are allowed to be used during the clinical study.
Other Medical Device or Medication Specified for Use During the Study. During the clinical study, additional contact lens solution is required in conjunction with the treatment: • AOSEPT PLUS with HydraGlyde Cleaning & Disinfecting Solution will be used for daily cleaning and disinfection.

Related to Other Medical Device or Medication Specified for Use During the Study

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  • Evaluation During the Probationary Period 1. At or about the time of the delivery of a probationary letter, the evaluator shall hold a personal conference with the probationary teacher to discuss performance deficiencies and the remedial measures to be taken.

  • Information and Services Required of the Owner § 3.1.1 The Owner shall provide information with reasonable promptness, regarding requirements for and limitations on the Project, including a written program which shall set forth the Owner’s objectives, constraints, and criteria, including schedule, space requirements and relationships, flexibility and expandability, special equipment, systems, sustainability and site requirements.

  • Certification Regarding Prohibition of Boycotting Israel (Tex Gov. Code 2271) If (a) Vendor is not a sole proprietorship; (b) Vendor has ten (10) or more full-time employees; and (c) this Agreement or any agreement with a TIPS Member under this procurement has value of $100,000 or more, the following certification shall apply; otherwise, this certification is not required. Vendor certifies, where applicable, that neither the Vendor, nor any affiliate, subsidiary, or parent company of Vendor, if any, boycotts Israel, and Vendor agrees that Vendor and Vendor Companies will not boycott Israel during the term of this Agreement. For purposes of this Agreement, the term “boycott” shall mean and include refusing to deal with, terminating business activities with, or otherwise taking any action that is intended to penalize, inflict economic harm on, or limit commercial relations with Israel, or with a person or entity doing business in Israel or in an Israeli-controlled territory but does not include an action made for ordinary business purposes. When applicable, does Vendor certify? Yes

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