PURE COMMERCIAL Sample Clauses

PURE COMMERCIAL. You envision commercial use for all the genetic resources accessed and you decide to negotiate the benefit sharing conditions for commercial use upon the access of the genetic resources. In this case only use article 4.3. (and delete articles 4.2 and 4.4.). By signing the agreement the provider country (1) gives the research consortium permission to sample in its waters and (2) enters into a partnership resulting in following automatic benefits for the provider country: • access to scientific results through open-access integrated databases • monetary benefits in case of proprietary use • benefits from legal certainty provided by the agreement • affiliation to a major international scientific bioinformatics network Additional benefits can be negotiated with the provider country relating to sampling, data analysis and management: • mentoring of the provider country scientists by Micro B3 scientists • participation of the provider country scientists in research activities related to the sampling activity and its analysis • participation of the provider country scientists in training for capacity building on bioinformatics, data management and data analysis • sample archiving for defined period of time • support for fund rising for sequencing, for finding sequencing partners and long-term archive partners The Micro B3 ABS model agreements also contain a viral license clause for improved monitoring of material transfer and data transfer to third parties. The viral licence concept means that the ABS contract travels with the resource and the data upon transfer. The Micro B3 model ABS agreements offer a viral license clause in article 5. This clause grants that all the obligations of the initial agreement will be imposed on subsequent use of the materials and the produced data when transferred. When the viral licence clause is used, then the scientist/scientific institution is allowed to transfer the material to third parties if they sign a new contract in which they commit themselves to respect the conditions of the initial ABS agreement. Every transfer to new third parties would require the signature of an MTA that makes the initial ABS agreement binding, to which the initial ABS should be attached as Annex. At each transfer however, according to the Nagoya Protocol, consent is required from the competent national authority in the provider country (Prior Informed Consent). Here two situations can be distinguished: • If you use the viral licence clause, a notif...
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PURE COMMERCIAL. The recipient envisions commercial uses for all the genetic resources accessed and decides to negotiate the benefit sharing conditions for commercial uses upon the access of the genetic resources. In this case only article 4.3. if the model contract applies (delete articles 4.2 – 4.4).
PURE COMMERCIAL. The recipient envisions commercial uses for all the genetic resources accessed and decides to negotiate the benefit sharing conditions for commercial uses upon the access of the genetic resources. In this case only article 4.3. if the model contract applies (delete articles 4.2 – 4.4). Core benefits By signing the agreement, the provider country gives the research consortium the permit to sample in its seas and enters into a partnership. In such partnership some mutual benefits are automatically included and others can be decided/negotiated while signing the agreement (in the specific conditions of article 4). These benefits are summarized below: Access to scientific results and data through open access integrated databases Additional monetary benefits in case of proprietary use as specified in the contract Benefits from the legal certainty provided by the agreement Be part of a major international scientific bio-informatics network Related to the sampling Mentoring of provider country scientists by MICRO B3 project scientists that provide information and training on sampling and sampling processing Participation of the provider country scientists in all the scientific research activities on the boat and on land related to the sampling activity and its analysis Archiving of the sampling for a certain period of time Possible support for finding sequencing partners/preferred long-term archive partners Related to the processing Possible collaboration with Argon national lab/other Support in fund raising from national funding agencies for sequencing (as an option, for a limited number of samples, additional support from the MICRO B3 consortium can be envisioned when there are major capacity gaps) Related to data management and integration and access Possible participation in training for capacity building on bioinformatics, data management and data analysis (MICRO B3 summary schools and workshops) Core elements of the MICRO B3 agreement

Related to PURE COMMERCIAL

  • Non Commercial You may not use this work for commercial purposes. No Derivative Works - You may not alter, transform, or build upon this work. Any of these conditions can be waived if you receive permission from the author. Your fair dealings and other rights are in no way affected by the above. If you believe that this document breaches copyright please contact xxxxxxxxxxx@xxx.xx.xx providing details, and we will remove access to the work immediately and investigate your claim.

  • Industry Troubleshooter Where a difference arises between the parties relating to the dismissal, discipline, or suspension of an employee, or to the interpretation, application, operation, or alleged violation of this Agreement, including any question as to whether a matter is arbitrable, during the term of the Collective Agreement, Xxxxx XxXxxxxxxx, Xxxx Xxxxxx, Xxxxx Xxxxxxxx, or a substitute agreed to by the parties, shall at the request of either party:

  • Commercial The detailed criteria is mentioned at 1.02 of Annexure-A to BDS at Volume-I : Section-III.

  • 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.

  • Diagnostic procedures to aid the Provider in determining required dental treatment.

  • 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.

  • 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.

  • Reasonable Commercial Efforts (a) Subject to the terms and ------------------------------ conditions provided in this Agreement, each party shall use reasonable commercial efforts to take promptly, or cause to be taken, all actions, and to do promptly, or cause to be done, all things necessary, proper or advisable under applicable laws and regulations to consummate and make effective the transactions contemplated hereby, to obtain all necessary waivers, consents and approvals and to effect all necessary registrations and filings, including, without limitation, an appropriate filing of a Notification and Report Form pursuant to the HSR Act with respect to the transactions contemplated hereby, and the filings and consents set forth on Schedule 6.4 hereto (the "Required ------------ -------- Consents") and to remove any injunctions or other impediments or delays, legal -------- or otherwise, in order to consummate and make effective the transactions contemplated by this Agreement for the purpose of securing to the parties hereto the benefits contemplated by this Agreement; provided that notwithstanding -------- anything to the contrary in this Agreement, no party nor any of their Affiliates shall be required to make any disposition, including, without limitation, any disposition of, or any agreement to hold separate, any Subsidiary, asset or business, and no party hereto nor any of their Affiliates shall be required to make any payment of money nor shall any party or its Affiliates be required to comply with any condition or undertaking or take any action which, individually or in the aggregate, would materially adversely affect the economic benefits to such party of the transactions contemplated hereby and the Implementing Agreements, taken as a whole or adversely affect any other business of such party or its Affiliates. (b) Each of the parties hereto shall execute and cause its Subsidiaries to execute on or prior to the Closing Date each Implementing Agreement to which it or they are a party on the terms set forth in the relevant Exhibits hereto. (c) Each of the parties hereto agrees, from time to time, to execute and deliver, or use reasonable commercial efforts to cause to be executed and delivered, such additional instruments, certificates or documents (including bills of sale and assignment and assumption agreements), and take all such actions, reasonably necessary to implement or effectuate the transactions contemplated by this Agreement.

  • Development and Commercialization Subject to Sections 4.6 and 4.7, Fibrocell shall be solely responsible for the development and Commercialization of Fibrocell Products and Improved Products. Fibrocell shall be responsible for all costs incurred in connection with the Fibroblast Program except that Intrexon shall be responsible for the following: (a) costs of establishing manufacturing capabilities and facilities in connection with Intrexon’s manufacturing obligation under Section 4.6 (provided, however, that Intrexon may include an allocable portion of such costs, through depreciation and amortization, when calculating the Fully Loaded Cost of manufacturing a Fibrocell Product, to the extent such allocation, depreciation, and amortization is permitted by US GAAP, it being recognized that the majority of non-facilities scale-up costs cannot be capitalized and amortized under US GAAP); (b) costs of basic research with respect to the Intrexon Channel Technology and Intrexon Materials (i.e., platform improvements) but, for clarity, excluding research described in Section 4.7 or research requested by the JSC for the development of a Fibrocell Product or an Improved Product (which research costs shall be reimbursed by Fibrocell); (c) [*****]; and (d) costs of filing, prosecution and maintenance of Intrexon Patents. The costs encompassed within subsection (a) above shall include the scale-up of Intrexon Materials and related active pharmaceutical ingredients for clinical trials and Commercialization of Fibrocell Products undertaken pursuant to Section 4.6, which shall be at Intrexon’s cost whether it elects to conduct such efforts internally or through Third Party contractors retained by either Intrexon or Fibrocell (with Intrexon’s consent).

  • Sustainable Development 4.1 The Authority will review the Contractor’s Sustainable Development Policy Statement and Sustainable Development Plan submitted by the Contractor in accordance with the Schedule (Sustainable Development Requirements) and then at least annually thereafter. 4.2 Sustainable Procurement Risk Assessment Methodology (SPRAM) is a tool used by the Authority to identify and mitigate any potential risks to sustainability in contracts. The process requires that each Contract be assessed for its potential social, economic and environmental risks, throughout the various stages of its lifetime. Where risks are identified, appropriate mitigation action is required to reduce or eliminate the risk to sustainability. The Authority may at times require input from the Contractor in order to ensure that this process is given the required levels of consideration.

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