Roche Basel definition

Roche Basel shall have the meaning set forth in the Preamble.
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Roche Basel has the meaning set forth in the recitals.
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Roche Basel has the meaning set forth in the Preamble of this Agreement.
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Examples of Roche Basel in a sentence

  • Nucleus were stained with DAPI (236276, Roche, Basel, Switzerland) at a dilution of 1:1000.

  • The resulting protoplasts were homogenized by sonication (3 times, 10 s at 8W) on ice and suspended in PBS with Completemini tablets containing a cocktail of protease inhibitors (Roche; Basel Switzerland).

  • In consideration for the rights granted to Roche under this Agreement, Roche Basel shall pay to Prothena Ireland a one-time, non-refundable, non-creditable payment of thirty million Dollars ($30,000,000), within [*] of the Effective Date and receipt by Roche Basel of an invoice for such amount from Prothena Ireland, by wire transfer of immediately available funds into an account designated in writing by Prothena Ireland.

  • Cells were then washed with ice-cold PBS and harvested with lysis buffer (50 mM Tris· HCl, pH 7.5, 1 mM EDTA, 1% Triton X-100) containing 1 mM PMSF, protease inhibitor cocktails (Roche, Basel, Switzerland), 1 mM sodium vanadate, and 200 nM okadaic acid.

  • Bovine serum albumin (BSA) was obtained from Boehringer Mannheim (now a part of Roche, Basel, Switserland) (735108), other proteins were obtained from Sigma Chemicals (Zwijndrecht, The Netherlands): ovalbumin (A5503), cytochrome c (C2037), lysozyme (L6876) and γ-globulin (G5009).

  • Previously, Dr. Platzer served as the business director of oncology, as well as the global strategic marketing and therapeutic area head of oncology at Roche, Basel.

  • As in [16], the animals were anesthetized via intramuscular injection of 0.5 mg/kg Diazepan (Valium®; Roche, Basel, Switzerland), 0.25 mg/kg metedomidine hydrochloride (Domitor; Virbac, Carros, France) and 100 mg/kg ketamine hydrochloride (Ketalar500®; Pfizer, New York, NY, USA).

  • Hookipa will deliver Materials to Roche under DAP (Roche Basel or Roche’s designee), Incoterms® 2020.

  • Sections were rinsed with PBS and incubated for 1 hr at RT with AlexaFluor#488 or AlexaFluor#594 conjugated polyclonal antirabbit/mouse antibodies (1:600, Jackson ImmunoResearch, RRID:AB_141708, RRID:AB_141633) and DAPI (1:1000,#10236276001, Hoffmann-La Roche, Basel, Switzerland) to label nuclei.

  • In its hearing, the SEC had requested him to disclose all information about the Roche group’s structure.73 The SEC demanded that he take responsibility for this information not as Presi- dent of Roche Basel but as an individual.

Related to Roche Basel

  • EU GDPR means Regulation (EU) 2016/679 of the European Parliament and of the Council of 27 April 2016 on the protection of natural persons with regard to the processing of personal data and on the free movement of such data, and repealing Directive 95/46/EC.

  • Designated Products means products provided by Motorola to Licensee with which or for which the Software and Documentation is licensed for use.

  • Clinical evaluation means a systematic and planned process to continuously generate, collect, analyse and assess the clinical data pertaining to a device in order to verify the safety and performance, including clinical benefits, of the device when used as intended by the manufacturer;

  • Clinical laboratory means a facility for the microbiological, serological, chemical, hematological, radiobioassay, cytological, immunohematological, pathological, or other examination of materials derived from the human body for the purpose of providing information for the diagnosis, prevention, or treatment of a disease or assessment of a medical condition.

  • Participating Clinical Laboratory means a Clinical Laboratory which has a written agreement with the Claim Administrator or another Blue Cross and/or Blue Shield Plan to provide services to you at the time services are rendered.

  • Physical therapy licensing board or "licensing board" means the agency of a state that is responsible for the licensing and regulation of physical therapists and physical therapist assistants.

  • Xxxx-Xxxxx Act means the Xxxx-Xxxxx Xxxx Street Reform and Consumer Protection Act.

  • Xxxxx–Xxxxx Act For any federally assisted construction contract, in excess of two thousand dollars ($2,000), the contractor, subcontractor, subrecipient shall comply with all of the requirements of the Xxxxx-Xxxxx Act (40 U.S.C. 3141 – 3148) as supplemented by Department of Labor Regulations (29 CFR Part 5, “Labor Standards Provisions Applicable to Contracts Covering Federally Financed and assisted Construction”); and the Xxxxxxxx “Anti-Kickback” Act (40 U.S.C. 3145), as supplemented by Department of Labor regulations (29 CFR Part 3, “Contractors and Subcontractors on Public Building or Public Work Financed in Whole or in Part by Loans or Grants from the United States”).

  • in vitro diagnostic medical device means any medical device which is a reagent, reagent product, calibrator, control material, kit, instrument, apparatus, equipment, software or system, whether used alone or in combination, intended by the manufacturer to be used in vitro for the examination of specimens, including blood and tissue donations, derived from the human body, solely or principally for the purpose of providing information:

  • Wholesale drug distributor means anyone engaged in the

  • Manufactured products means items and construction materials composed in whole or in part of non-ferrous metals such as aluminum; plastics and polymer-based products such as polyvinyl chloride pipe; aggregates such as concrete; glass, including optical fiber; and lumber.

  • veterinary surgeon means a veterinary surgeon within the meaning of the Veterinary Surgeons Act 1936.

  • Sxxxxxxx-Xxxxx Act means the Sxxxxxxx-Xxxxx Act of 2002, as amended.

  • PHSA means the United States Public Health Service Act, as amended from time to time.

  • Hemp products means all products made from industrial hemp,

  • Clinical review criteria means the written screening procedures, decision abstracts, clinical protocols, and practice guidelines used by a health carrier to determine the necessity and appropriateness of health care services.

  • Reformulated Products means Products that contain concentrations less than or equal to 0.1% (1,000 parts per million (ppm)) of DEHP when analyzed pursuant to U.S. Environmental Protection Agency testing methodologies 3580A and 8270C or other methodology utilized by federal or state government agencies for the purpose of determining the phthalate content in a solid substance.

  • Covered Products means Your Applications, Libraries, Passes, Safari Extensions, Safari Push Notifications, and/or FPS implementations developed under this Agreement.

  • Phase 4 Clinical Trial means a Clinical Trial of a Product conducted after Regulatory Approval of such Product has been obtained from an appropriate Regulatory Authority, which trial is (a) conducted voluntarily by a Party to enhance marketing or scientific knowledge of the Product, or (b) conducted due to a request or requirement of a Regulatory Authority.

  • Xxxxxxxx-Xxxxx Act means the Xxxxxxxx-Xxxxx Act of 2002.

  • Commercialization or “Commercialize” means activities directed to marketing, promoting, research and development as required, manufacturing for sale, offering for sale, distributing, importing or selling a product, including sub-licensing or sub-contracting of these activities.

  • Pivotal Clinical Trial means a human clinical trial in any country that is prospectively designed to generate data intended to satisfy the requirements of 21 C.F.R. § 312.21(c) (as amended) in the U.S. or a similar clinical study prescribed by a Regulatory Authority from another country, from time to time, pursuant to Applicable Law.

  • Xxxxxxx Act means the Xxxxxxx Antitrust Act of 1890.

  • Non-Participating Clinical Laboratory means a Clinical Laboratory which does not have a written agreement with the Claim Administrator or another Blue Cross and/or Blue Shield Plan provide services to you at the time services are rendered.

  • Collaborative drug therapy management means participation by an authorized pharmacist and a physician in the management of drug therapy pursuant to a written community practice protocol or a written hospital practice protocol.

  • Marihuana-infused product means a topical formulation, tincture, beverage, edible substance, or similar product containing marihuana and other ingredients and that is intended for human consumption.