Advanced Manufacturing Sample Clauses

Advanced Manufacturing. Notwithstanding anything to the contrary contained herein or (if executed) in the DM License Agreement for DM1, if Xxxxxxxx reserves a Manufacturing slot as described in Section 2.10(a), Millennium may by written notice to Xxxxxxxx (a “Manufacturing Notice”) request Xxxxxxxx [***] to timely Manufacture (or have Manufactured) and supply to Millennium an amount of DM1 Manufactured utilizing the Manufacturing slot reserved by Xxxxxxxx pursuant to Section 2.10(a) (“Advanced Manufacturing Services”). Xxxxxxxx will reasonably consider the request set forth in Millennium’s Manufacturing Notice and will negotiate [***] with Millennium to enter into separate quality and supply agreements with Millennium, which are satisfactory to Xxxxxxxx, for the Advanced Manufacturing Services as contemplated below, provided no Advanced Manufacturing Services will commence unless or until the Parties execute such separate quality and supply agreements. Millennium may deliver a Manufacturing Notice at any time during the DM Option Term with respect to DM1 or, in the event that Millennium delivers an Exercise Notice to Xxxxxxxx with respect to DM1, after the expiration thereof and prior to the date that is [***] after the effective date of the DM License Agreement for DM1. Following Xxxxxxxx’x reservation of the Manufacturing slot pursuant to Section 2.10(a) and through the date [***] following Xxxxxxxx’x receipt of a Manufacturing Notice, the Parties will [***] negotiate and enter into separate quality and supply agreements with respect to the Advanced Manufacturing Services contemplated under this Section 2.10(h), which shall (i) contain supply terms reasonably acceptable to the Parties, including that [***] and (ii) be consistent with the terms of this Section 2.10(h) and Millennium’s policies. Xxxxxxxx shall, during the period in which the Parties negotiate the separate quality and supply agreements referenced in the immediately preceding paragraph and following such period, if the Parties enter into such separate quality and supply agre ement, as set forth in such separate quality and supply agreements, provide Millennium with such full access to its (and its Third Party CMO’s) sites, facilities, production, operations, testing, storage, books and records, quality system and any other information as is necessary or useful in order for Millennium to perform to its satisfaction a formal quality assessment and/or quality audit in respect of Xxxxxxxx’x Manufacturing and supply obl...
Sample 1
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Advanced Manufacturing.  CETA makes goods manufactured by Ontario companies more competitive in the EU market by eliminating tariffs on a wide range of industrial products of interest to the Ontario, such as: Pre-CETA tariffs Under CETA  CETA provides clear and simple rules of origin which Ontario companies can use to determine qualification of its products for CETA benefits, as well as access to advance rulings on rules of origin and tariff classifications for its products.  Ontario exporters will be able to have certain goods tested to EU standards by a certification body in Canada, and the results of the tests will be recognized by the EU, thereby avoiding testing duplication and minimizing costs.  Before CETA, EU tariffs could be complex and prohibitive for many Ontario processed food manufacturers, for example: *EA and AD S/Z: Additional specific duties which vary depending on the amount of dairy and/or grain and/or sugar in the produc t. MAX: Maximum applied EA tariff.  CETA immediately eliminated all EU tariffs on processed foods (with the exception of sweet and corn and refined sugar), providing food manufacturers with an advantage over many competitors entering the EU market.  Under CETA, 94% of EU agriculture tariff lines have become duty-free, providing Ontario exporters with an advantage over many competitors in the EU market. Many remaining EU tariff lines will be phased out over a period of 7 years.  CETA’s comprehensive tariff elimination plays to many of the region’s strengths, such as: Pre-CETA tariffs Under CETA * During the 7-year phase out, a transitional duty-free TRQ of 100,000 tonnes will be established for low-medium quality wheat. After which, it will be duty-free and quota free. For high quality wheat, current EU tariffs are applied at 0% but may increase as they are subject to the EU’s Intervention Price System (I-55). Tariffs on high quality wheat will be phased out over 7 years under CETA.  In addition, CETA establishes tariff rate quotas (TRQs) for specific products, providing Ontario producers duty-free access for specific volumes of products, including: TRQ Phase-In Period * A duty-free free TRQ of 35,000 tonnes for fresh/chilled beef and veal and 15,000 tonnes for frozen beef and veal are established under CETA. In addition, the EU immediately eliminated the 20% tariff on Canadian exports of high-quality beef under the EU’s existing WTO quota (11,500 tonnes (product weight) shared with the United States, commonly referred to as the Hilton ...
Sample 1
Advanced Manufacturing. The agreement provides $25,000,000 for the Energy-Water De- salination Hub and provides up to $10,000,000 to be used to issue a competitive solicitation for university and industry-led teams to im- prove the efficiency of industrial drying processes.
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Advanced Manufacturing. Advanced manufacturing presents an opportunity for Australia and Israel to collaboratively improve products and processes with innovative and cutting-edge technology. Both countries are well placed to partner together for the mutual benefit. Advanced manufacturing accounts for roughly half of Australia’s $100 billion annual manufacturing output.11 The success of Australia’s advanced manufacturing is in part due to the collaboration with R&D institutions and the manufacturing sector. Advanced manufacturing in Israel is highly advanced in relation to digital systems such as Internet Of Things, cyber security and AI. Utilising this expertise from Israel can consolidate Australia’s industry 4.0-driven manufacturing sector through commercial partnerships.
Sample 1
Advanced Manufacturing. The College is leading the development of a coherent approach to ensure employers have the skilled workforce required in the aforementioned areas. This involves working in partnership with schools, third sector and universities to develop a pipeline of talent with a focus in above areas. In North Ayrshire, XLCC, based at Hunterston, is working in partnership with the College to increase the number of Performing Engineering Operations (PEO) courses available to prospective students across Ayr, Kilmarnock and Kilwinning campuses. Additional course content was provided in partnership their specialist training provider who delivered train the trainer sessions for college staff in the Spring of 2023 on cable manufacturing fundamentals. Once fully operational in 2025, the XLCC facility will support 900 jobs in the Hunterston area, with thousands more in the wider supply chain. Renewable technology, including a cutting-edge hybrid air source installation has been donated by industry partners and almost all staff have been upskilled in both qualifications and manufacturers training. This will allow the College to roll out re- skilling and upskilling in renewable heat technologies in the current academic year. In addition, Motor Vehicle staff have completed the PDA Hydrogen: An Introduction for Technicians SCQF level 7 offered through Energy Skills Partnership which will also enable reskilling and upskilling learning opportunities to be offered in this area. Ayrshire College, North Ayrshire Council, the Magnox Socio Economic Panel, the Scottish Funding Council and the Ayrshire College Foundation have worked in partnership to provide funding for The Xxxxxx Xxxxxx Skills Hub which will open in August 2023. This partnership approach has created the opportunity for the first time for North Ayrshire communities to access Modern Apprenticeships, firstly in Carpentry and Joinery. In AY 2023-24, The College will deliver to ten apprentices from Ayrshire company Xxxxx Xxxx LTD. The College is leading the development of a coherent approach to ensure employers have the skilled workforce required in the aforementioned areas. This involves working in partnership with schools, third sector and universities to develop a pipeline of talent. Specifically in the aerospace sector, the College has a critical role to play in providing the sector with a pipeline of appropriately skilled people and is a key partner in the long-term economic ambitions of Ayrshire to be a recognised global ...
Sample 1
Advanced Manufacturing. The Advanced Manufacturing Innovation Centre - a £100m investment under Belfast Region City Deal - is a collaborative, innovative powerhouse of advanced manufacturing set to elevate our region globally. AMIC is supporting economic growth and prosperity for Northern Ireland by creating high quality jobs and increasing inward investment through high value manufacturing innovation clusters throughout the region. The Centre will drive industrial transformation, paving the way for future technologies and competing globally with a more sustainable focus. AMIC is key to an exciting future for manufacturing in this region. It builds on 50 years of sustained innovation and industry support through the Northern Ireland Technology Centre (NITC), the Polymers Processing Research Centre (PPRC) and the more recent university- industry partnership, NI Advanced Composites and Engineering (NIACE) as well as UK- leading research capability in smart design and nanotech and photonics. AMIC is on track to open a 10,500m2 state-of-the-art Factory of the Future at Global Point Business Park in Newtownabbey in 2026. Designed for industry, the open access manufacturing and engineering innovation centre will reinvigorate Northern Ireland’s industrial potential and address the future technology and skills challenges faced by the region’s manufacturing sector. It will provide a specialised environment for advanced manufacturing, materials, and engineering sectors to access the latest digital, automation and robotics technology supported by experienced engineers and underpinned by academic excellence. Throughout 2024/25 AMIC’s development will focus on progressing the following: • A successfully functioning Learning Factory engaging a diverse range of industry, community and education groups. • A collaborative plan and skills portfolio based on intelligence around skills gaps and future skills needs across Northern Ireland. • Increased productivity and high value jobs. • More people and enhanced diversity entering into Advanced Manufacturing pathways and jobs. • Increased options and take up of apprenticeship pathways which are joined up and responsive to industry need.
Sample 1
Advanced Manufacturing.  CETA makes goods manufactured by the region’s companies more competitive in the EU market.
Sample 1
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Related to Advanced Manufacturing

  • Manufacturing (a) The Supplier shall without limitation be responsible, at no additional cost to the Purchaser, for: sourcing and procuring all raw materials for the Products; obtaining all necessary approvals, permits and licenses for the manufacturing of the Products; providing sufficient qualified staff and workers to perform the obligations under this Purchase Agreement; implementing and maintaining effective inventory and production control procedures with respect to the Products; and handling other matters as reasonably requested by the Purchaser from time to time. (b) The Supplier shall not change any process, material, component, packaging or manufacturing location without the Purchaser’s express prior written approval.

  • API If the Software offers integration capabilities via an API, your use of the API may be subject to additional costs or Sage specific policies and terms and conditions (which shall prevail in relation to your use of the API). You may not access or use the API in any way that could cause damage to us or the Software, or in contravention of any applicable laws. We reserve the right in our sole discretion, to: (i) update any API from time to time; (ii) place limitations around your use of any API; and (iii) deny you access to any API in the event of misuse by you or to otherwise protect our legitimate interests.

  • Manufacturing Services Jabil will manufacture the Product in accordance with the Specifications and any applicable Build Schedules. Jabil will reply to each proposed Build Schedule that is submitted in accordance with the terms of this Agreement by notifying Company of its acceptance or rejection within three (3) business days of receipt of any proposed Build Schedule. In the event of Jabil’s rejection of a proposed Build Schedule, Jabil’s notice of rejection will specify the basis for such rejection. When requested by Company, and subject to appropriate fee and cost adjustments, Jabil will provide Additional Services for existing or future Product manufactured by Jabil. Company shall be solely responsible for the sufficiency and adequacy of the Specifications [***].

  • PRODUCT MANUFACTURER'S SUPPLIERS Only those dealers/distributors listed by the manufacturer will be considered authorized to act on behalf of the Product Manufacturer.

  • Durable Medical Equipment (DME), Medical Supplies, Prosthetic Devices, Enteral Formula or Food, and Hair Prosthesis (Wigs) This plan covers durable medical equipment and supplies, prosthetic devices and enteral formula or food as described in this section. DME is equipment which: • can withstand repeated use; • is primarily and customarily used to serve a medical purpose; • is not useful to a person in the absence of an illness or injury; and • is for use in the home. DME includes supplies necessary for the effective use of the equipment. This plan covers the following DME: • wheelchairs, hospital beds, and other DME items used only for medical treatment; and • replacement of purchased equipment which is needed due to a change in your medical condition or if the device is not functional, no longer under warranty, or cannot be repaired. DME may be classified as a rental item or a purchased item. In most cases, this plan only pays for a rental DME up to our allowance for a purchased DME. Repairs and supplies for rental DME are included in the rental allowance. Medical supplies are consumable supplies that are disposable and not intended for re- use. Medical supplies require an order by a physician and must be essential for the care or treatment of an illness, injury, or congenital defect. Covered medical supplies include: • essential accessories such as hoses, tubes and mouthpieces for use with medically necessary DME (these accessories are included as part of the rental allowance for rented DME); • catheters, colostomy and ileostomy supplies, irrigation trays and surgical dressings; and • respiratory therapy equipment. This plan covers diabetic equipment and supplies for the treatment of diabetes in accordance with R.I. General Law §27-20-30. Covered diabetic equipment and supplies include: • therapeutic or molded shoes and inserts for custom-molded shoes for the prevention of amputation; • blood glucose monitors including those with special features for the legally blind, external insulin infusion pumps and accessories, insulin infusion devices and injection aids; and • lancets and test strips for glucose monitors including those with special features for the legally blind, and infusion sets for external insulin pumps. The amount you pay differs based on whether the equipment and supplies are bought from a durable medical equipment provider or from a pharmacy. See the Summary of Pharmacy Benefits and the Summary of Medical Benefits for details. Coverage for some diabetic equipment and supplies may only be available from either a DME provider or from a pharmacy. Visit our website to determine if this is applicable or call our Customer Service Department. Prosthetic devices replace or substitute all or part of an internal body part, including contiguous tissue, or replace all or part of the function of a permanently inoperative or malfunctioning body part and alleviate functional loss or impairment due to an illness, injury or congenital defect. Prosthetic devices do not include dental prosthetics. This plan covers the following prosthetic devices as required under R.I. General Law § 27-20-52: • prosthetic appliances such as artificial limbs, breasts, larynxes and eyes; • replacement or adjustment of prosthetic appliances if there is a change in your medical condition or if the device is not functional, no longer under warranty and cannot be repaired; • devices, accessories, batteries and supplies necessary for prosthetic devices; • orthopedic braces except corrective shoes and orthotic devices used in connection with footwear; and • breast prosthesis following a mastectomy, in accordance with the Women’s Health and Cancer Rights Act of 1998 and R.I. General Law 27-20-29. The prosthetic device must be ordered or provided by a physician, or by a provider under the direction of a physician. When you are prescribed a prosthetic device as an inpatient and it is billed by a provider other than the hospital where you are an inpatient, the outpatient benefit limit will apply. Enteral formula or food is nutrition that is absorbed through the intestinal tract, whether delivered through a feeding tube or taken orally. Enteral nutrition is covered when it is the sole source of nutrition and prescribed by the physician for home use. In accordance with R.I. General Law §27-20-56, this plan covers enteral formula taken orally for the treatment of: • malabsorption caused by Crohn’s Disease; • ulcerative colitis; • gastroesophageal reflux; • chronic intestinal pseudo obstruction; and • inherited diseases of amino acids and organic acids. Food products modified to be low protein are covered for the treatment of inherited diseases of amino acids and organic acids. Preauthorization may be required. The amount that you pay may differ depending on whether the nutrition is delivered through a feeding tube or taken orally. When enteral formula is delivered through a feeding tube, associated supplies are also covered. This plan covers hair prosthetics (wigs) worn for hair loss suffered as a result of cancer treatment in accordance with R.I. General Law § 27-20-54 and subject to the benefit limit and copayment listed in the Summary of Medical Benefits. This plan will reimburse the lesser of the provider’s charge or the benefit limit shown in the Summary of Medical Benefits. If the provider’s charge is more than the benefit limit, you are responsible for paying any difference. This plan covers Early Intervention Services in accordance with R.I. General Law §27- 20-50. Early Intervention Services are educational, developmental, health, and social services provided to children from birth to thirty-six (36) months. The child must be certified by the Rhode Island Department of Human Services (DHS) to enroll in an approved Early Intervention Services program. Services must be provided by a licensed Early Intervention provider and rendered to a Rhode Island resident. Members not living in Rhode Island may seek services from the state in which they reside; however, those services are not covered under this plan. Early Intervention Services as defined by DHS include but are not limited to the following: • speech and language therapy; • physical and occupational therapy; • evaluation; • case management; • nutrition; • service plan development and review; • nursing services; and • assistive technology services and devices.

  • Manufacture 2.1. The LED(s) on the LED module shall be equipped with suitable fixation elements. 2.2. The fixation elements shall be strong and firmly secured to the LED(s) and the LED module.

  • Product ACCEPTANCE Unless otherwise provided by mutual agreement of the Authorized User and the Contractor, Authorized User(s) shall have thirty (30) days from the date of delivery to accept hardware products and sixty (60) days from the date of delivery to accept all other Product. Where the Contractor is responsible for installation, acceptance shall be from completion of installation. Failure to provide notice of acceptance or rejection or a deficiency statement to the Contractor by the end of the period provided for under this clause constitutes acceptance by the Authorized User(s) as of the expiration of that period. The License Term shall be extended by the time periods allowed for trial use, testing and acceptance unless the Commissioner or Authorized User agrees to accept the Product at completion of trial use. Unless otherwise provided by mutual agreement of the Authorized User and the Contractor, Authorized User shall have the option to run testing on the Product prior to acceptance, such tests and data sets to be specified by User. Where using its own data or tests, Authorized User must have the tests or representative set of data available upon delivery. This demonstration will take the form of a documented installation test, capable of observation by the Authorized User, and shall be made part of the Contractor’s standard documentation. The test data shall remain accessible to the Authorized User after completion of the test. In the event that the documented installation test cannot be completed successfully within the specified acceptance period, and the Contractor or Product is responsible for the delay, Authorized User shall have the option to cancel the order in whole or in part, or to extend the testing period for an additional thirty (30) day increment. Authorized User shall notify Contractor of acceptance upon successful completion of the documented installation test. Such cancellation shall not give rise to any cause of action against the Authorized User for damages, loss of profits, expenses, or other remuneration of any kind. If the Authorized User elects to provide a deficiency statement specifying how the Product fails to meet the specifications within the testing period, Contractor shall have thirty (30) days to correct the deficiency, and the Authorized User shall have an additional sixty (60) days to evaluate the Product as provided herein. If the Product does not meet the specifications at the end of the extended testing period, Authorized User, upon prior written notice to Contractor, may then reject the Product and return all defective Product to Contractor, and Contractor shall refund any monies paid by the Authorized User to Contractor therefor. Costs and liabilities associated with a failure of the Product to perform in accordance with the functionality tests or product specifications during the acceptance period shall be borne fully by Contractor to the extent that said costs or liabilities shall not have been caused by negligent or willful acts or omissions of the Authorized User’s agents or employees. Said costs shall be limited to the amounts set forth in the Limitation of Liability Clause for any liability for costs incurred at the direction or recommendation of Contractor.

  • Manufacture of Products All Products marketed through Grantor's Web ------------------------- Site shall be manufactured, packaged, prepared, and shipped in accordance with the specifications and requirements described on Exhibit A hereto as it may be modified from time to time. Quality control standards relating to the Product's weight, color, consistency, micro-biological content, labeling and packaging are also set forth on Exhibit A. In the event that Exhibit A is incomplete, Products shall be manufactured and shipped in accordance with industry standards.

  • Product Labeling The labeling of all Licensed Products sold or offered for sale under this Agreement shall expressly state that the Licensed Product is manufactured under a license from the Medicines Patent Pool.

  • Raw Materials A. Catalent shall procure Raw Materials only from vendors that are approved in writing by Palatin or otherwise qualified in accordance with the provisions of the Quality Agreement. Catalent shall be responsible for procuring Raw Materials as necessary to meet the Firm Commitment. Catalent shall not be liable for any delay in delivery of Product if (i) Catalent is unable to obtain, in a timely manner, a particular Raw Material necessary for Processing and (ii) Catalent placed orders for such Raw Materials promptly following receipt of Palatin’s Firm Commitment. In the event that any Raw Material becomes subject to purchase lead time beyond the Firm Commitment time frame, the parties will negotiate in good faith an appropriate amendment to this Agreement, including Clause 4.2. B. In certain instances, Palatin may require a specific supplier, manufacturer or vendor (“Vendor”) to be used for Raw Material. In such an event, (i) such Vendor will be identified in the Specifications and (ii) the Raw Materials from such Vendor shall be deemed Palatin-supplied Materials for purposes of this Agreement. If the cost of the Raw Material from any such Vendor (other than a Vendor specified in the Specifications as of the Effective Date) is greater than Catalent’s costs for the same raw material of equal quality from other vendors, Catalent shall add the difference between Catalent’s cost of the Raw Material and the Vendor’s cost of the Raw Material to the Unit Pricing. Palatin will be responsible for all reasonable, out-of-pocket costs incurred by Catalent associated with qualification of any such Vendor who has not been previously qualified by Catalent. C. In the event of (i) a Specification change for any reason, (ii) obsolescence of any Raw Material or (iii) termination or expiry of this Agreement, Palatin shall bear the cost of any unused Raw Materials (including packaging), so long as Catalent (a) purchased such Raw Materials in quantities consistent with Palatin’s then current Firm Commitment and any minimum purchase obligations required by the vendor and (b) used commercially reasonable efforts to mitigate such costs by using any such unused Raw Materials in the manufacture of other products.

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