Manufacturing, Packaging, and Labeling Sample Clauses

Manufacturing, Packaging, and Labeling. 7.1 If environmental conditions could reasonably be expected to have an adverse effect on product quality, the Supplier shall establish and maintain procedures, to adequately control these environmental conditions. The Supplier shall keep records of these activities and make them available to Venus Concept Ltd. upon request.
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Manufacturing, Packaging, and Labeling. BIOCODEX shall manufacture the Products according to French and EU current good manufacturing practices (cGMP) and in compliance with the Specifications and with the local applicable manufacturing regulation as communicated in writing by DISTRIBUTOR. DISTRIBUTOR warrants to BIOCODEX that it has informed BIOCODEX in writing of all laws and regulations affecting the manufacture, sale, packaging and labeling of the Products which are in force in the Territory at the Effective Date in sufficient detail to enable BIOCODEX to comply with such laws and regulations regarding its activities under this Agreement. Additional relevant local regulations applicable in the Territory shall be notified in writing by DISTRIBUTOR to BIOCODEX prior to their coming into force and as much in advance as possible for BIOCODEX to comply with them in a timely manner. Products shall be supplied to DISTRIBUTOR accompanied by the appropriate certificate of analysis, attesting that the Products have been manufactured and tested in compliance with the EU cGMP requirements and with the related Marketing Authorizations as known to BIOCODEX. BIOCODEX shall supply the Products in finished packaged form. DISTRIBUTOR shall provide BIOCODEX with the information necessary to design the final packaging and labelling of the Products in accordance with any applicable regulations currently in force. However, BIOCODEX shall decide the packaging and the labelling of the Products on its own provided that they are compliant with applicable laws as mentioned in writing in a timely manner by DISTRIBUTOR. In order to ensure scientific and technical coherence of the communication being made regarding the Products worldwide, DISTRIBUTOR agrees to submit all promotional material related to the Products to BIOCODEX for its approval prior to their printing. Notwithstanding the foregoing, DISTRIBUTOR shall be fully responsible for the content of the promotional material used in the Territory.
Sample 1
Manufacturing, Packaging, and Labeling. 7.1 lf environmental conditions could reasonably be expected to have an adverse effect on product quality, the Supplier shall establish and maintain procedures, to adequately control these environmental conditions. The Supplier shall keep records of these activities and make them available to Venus Concept Ltd. upon request.
Sample 1
Manufacturing, Packaging, and Labeling. 7.1. Prima BioMed and its Affiliates shall manufacture the Products according to the requirements of Good Manufacturing Practices (GMP), in conformity to the Specifications for the Products and the warranties contained herein.
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Manufacturing, Packaging, and Labeling 
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Related to Manufacturing, Packaging, and Labeling

  • Packaging and Labeling Seller shall properly xxxx, xxxx, and ship Goods and provide Buyer with shipment documentation showing the Order number, Seller’s identification number for the subject Goods, the quantity of goods in shipment and the number of cartons or containers in the shipment.

  • Labeling and Packaging Seller shall label and package Products in accordance with applicable Legal Requirements and Specifications and shall include a unique identifying lot number.

  • 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 (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.

  • Product Specifications The Company agrees that all Products sold to Xxxx hereunder shall conform to the respective specifications set forth on Schedule A or to such other specifications as are from time to time agreed upon by the Parties.

  • Marketing Materials (a) During the term of this Agreement, the Sub-Adviser agrees to furnish the Manager at its principal office for prior review and approval by the Manager all written and/or printed materials, including but not limited to, PowerPointÒ or slide presentations, news releases, advertisements, brochures, fact sheets and other promotional, informational or marketing materials (the “Marketing Materials”) for internal use or public dissemination, that are produced or are for use or reference by the Sub-Adviser, its affiliates or other designees, broker-dealers or the public in connection with the Series, and Sub-Adviser shall not use any such materials if the Manager reasonably objects in writing within five business days (or such other period as may be mutually agreed) after receipt thereof. Marketing Materials may be furnished to the Manager by first class or overnight mail, facsimile transmission equipment, electronic delivery or hand delivery.

  • Manufacturing and Marketing Rights The Company has not granted rights to manufacture, produce, assemble, license, market, or sell its products to any other person and is not bound by any agreement that affects the Company's exclusive right to develop, manufacture, assemble, distribute, market, or sell its products.

  • Packaging Tangible product shall be securely and properly packed for shipment, storage, and stocking in appropriate, clearly labeled, shipping containers and according to accepted commercial practice, without extra charge for packing materials, cases, or other types of containers. All containers and packaging shall become and remain Customer’s property.

  • Labeling Upon request, Lessee will xxxx the Equipment indicating Lessor's interest with labels provided by Lessor. Lessee will keep all Equipment free from any other marking or labeling which might be interpreted as a claim of ownership.

  • Manufacturing and Supply Genentech shall be responsible for manufacturing and supplying Licensed Products for clinical use and commercial sale in the Genentech Field.

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