Diagnostic Impression Sample Clauses

Diagnostic Impression. 16. Is there any abnormality of the following: (CIRCLE APPLICABLE ITEMS AND GIVE DETAILS) Yes No (a) Eyes, ears, nose, mouth, pharynx.............. [_] [_] (IF VISION OR HEARING MARKEDLY IMPAIRED, INDICATE DEGREE AND CORRECTION) (b) Skin (incl. scars); lymph nodes; blood vessels...................................... [_] [_] (INCL. VARICOSE VEINS) (c) Nervous system (INCLUDE REFLEXES, GAIT, PARALYSIS)................................... [_] [_] (d) Respiratory system........................... [_] [_] (e) Abdomen (INCLUDING SCARS OR HERNIAS)......... [_] [_] (f) Genitourinary system......................... [_] [_] (g) Endocrine system (INCLUDE THYROID AND BREASTS)..................................... [_] [_] (h) Musculoskeletal system....................... [_] [_] (INCLUDE SPINE, JOINTS, AMPUTATIONS, DEFORMITIES) ------------------------------------------------------------------- 17. Have you any pertinent information not brought out above?........................................ [_] [_] ------------------------------------------------------------------------------------------------------------------------------------ MEDICAL EXAMINER: EXAMINER'S NAME AND OFFICE ADDRESS (PLEASE PRINT) X_________________________________________________ Name___________________________________________________________ SIGNATURE OF MEDICAL EXAMINER Street_________________________________________________________ WHEN PAYING FEES WE ARE REQUIRED TO SHOW AND REPORT SOCIAL SECURITY OR EMPLOYER I.D. NUMBER. PLEASE City___________________________________________________________ GIVE US THIS INFORMATION BELOW. Include All Hyphens [_____________________________] State__________________________________________________________
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Related to Diagnostic Impression

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  • Licensed Product “Licensed Product” shall mean any article, composition, apparatus, substance, chemical material, method, process or service whose manufacture, use, or sale is covered or claimed by a Valid Claim within the Patent Rights. For clarity, a “Licensed Product” shall not include other product or material that (a) is used in combination with Licensed Product, and (b) does not constitute an article, composition, apparatus, substance, chemical material, method, process or service whose manufacture, use, or sale is covered or claimed by a Valid Claim within the Patent Rights.

  • Field The term “

  • Licensed Products Lessee will obtain no title to Licensed Products which will at all times remain the property of the owner of the Licensed Products. A license from the owner may be required and it is Lessee's responsibility to obtain any required license before the use of the Licensed Products. Lessee agrees to treat the Licensed Products as confidential information of the owner, to observe all copyright restrictions, and not to reproduce or sell the Licensed Products.

  • Commercialization Intrexon shall have the right to develop and Commercialize the Reverted Products itself or with one or more Third Parties, and shall have the right, without obligation to Fibrocell, to take any such actions in connection with such activities as Intrexon (or its designee), at its discretion, deems appropriate.

  • Research Collaboration (a) GSK hereby grants to Anacor a non-exclusive, non-royalty bearing license under the GSK IP, solely as and to the extent necessary or important to conduct activities for which Anacor is responsible under the Research Plans during the Research Collaboration Term.

  • Product The term “

  • Licensed Technology The term "Licensed Technology" shall mean the ------------------- Licensed Patents, plus all improvements thereto developed by Licensor, and all related data, know-how and technology.

  • Marking of Licensed Products To the extent commercially feasible and consistent with prevailing business practices, Company shall xxxx, and shall cause its Affiliates and Sublicensees to xxxx, all Licensed Products that are manufactured or sold under this Agreement with the number of each issued patent under the Patent Rights that applies to such Licensed Product.

  • Manufacturing Technology Transfer With respect to each Technology Transfer Product, upon AbbVie’s written request after the Inclusion Date for the Included Target to which such Technology Transfer Product is Directed, Morphic shall effect a full transfer to AbbVie or its designee (which designee may be an Affiliate or a Third Party manufacturer) of all Morphic Know-How and Joint Know-How relating to the then-current process for the Manufacture of such Technology Transfer Product (the “Manufacturing Process”) and to implement the Manufacturing Process at facilities designated by AbbVie (such transfer and implementation, as more fully described in this Section 5.3, the “Manufacturing Technology Transfer”). To assist with the Manufacturing Technology Transfer, Morphic will make its personnel reasonably available to AbbVie during normal business hours for up to [***] FTE hours with respect to each Included Target (in each case, free of charge to AbbVie) to transfer and implement the Manufacturing Process under this Section 5.3. Thereafter, if requested by AbbVie, Morphic shall continue to perform such obligations; provided, that AbbVie will reimburse Morphic for its full-time equivalent (FTE) costs (for clarity, in excess of [***] FTE hours) and any reasonable and verifiable out-of-pocket costs incurred in providing such assistance. CERTAIN CONFIDENTIAL INFORMATION CONTAINED IN THIS DOCUMENT, MARKED BY [***], HAS BEEN OMITTED BECAUSE IT IS NOT MATERIAL AND WOULD LIKELY CAUSE COMPETITIVE HARM TO THE COMPANY IF PUBLICLY DISCLOSED.

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