Reporting etc. 13.01 For all activities performed under the Licence, the Licensee shall submit data, reports etc. to the MRA regarding all geological, geochemical, geophysical, technical, environmental, health, financial, including socio-economic, and other studies that are carried out in respect of the Licence Area, see section 86(4) of the Mineral Resources Act and section 13.03. At the MRA's request, the Licensee shall submit geological samples to the MRA, including drill cores.
Reporting etc. 3.10 To keep the Principal fully informed of its activities concerning the promotion and sale of the Products and to provide the Principal with reports on request.
Reporting etc. 16.01 For all activities performed under this Licence, the Licensee shall submit data, reports etc. to the Government of Greenland regarding all geological, geochemical, geophysical, technical, environmental, health, financial, including socio-economic, and other studies that are performed in respect of the Licence Area and/or activities under this Licence, see section 86(4) of the Mineral Resources Act and section
Reporting etc. In this version of the Tuition Agreement, the commitments of each party are grouped together for easier reference. It is in this section that issues specific to the needs of First Nation pupils for programs and services from the Board are delineated. The clauses which are included are intended to ensure that the Board will be addressing the specific concerns and circumstances of the First Nation with respect to the education of their children while they attend the schools of the Board. The primary responsibility for identifying those local issues and concerns rests with the First Nation. The list below of the commitments made by the Board is certainly not intended to be exhaustive. In fact, the list is primarily based on the assumption that this will be an agreement between one Board and one First Nation. In agreements between one Board and multiple First Nations, it may be possible, and even desirable, to negotiate other items which would not normally be part of an agreement with a single First Nation. The Addenda section of this sample agreement contains some items which might more successfully be negotiated, and implemented, in a multiple First Nation contract. The financial commitment clauses contained in this section have been cross-referenced with the Tuition Scoping Study project, being conducted as part of the overall NAN strategy, to ensure that they are both accurate and current. Covenants of the Board
Reporting etc. Purchaser shall have the responsibility in the Territory for complying with all regulatory filings, reporting requirements and other matters which relate solely to Purchaser’s acting as a distributor of the Product in the Territory. In the event Purchaser determines that it is required to file this Agreement with the United States Securities and Exchange Commission, Purchaser shall provide Seller with reasonable prior notice of such requirement and shall request confidential treatment of the financial terms and other competitively sensitive or trade secret terms of this Agreement. All other regulatory reporting matters (including adverse event and product complaint reporting) shall be Seller’s responsibility. Purchaser represents and warrants that Purchaser has in place systems and resources for tracking and reporting any adverse events with respect to the Product, such systems and resources to be consistent with good commercial standards in the pharmaceutical industry. Purchaser shall notify Seller of receipt of any report(s) of adverse events or product complaints pursuant to a Pharmacovigilance Agreement. To the extent that any inconsistencies exist between the Pharmacovigilance Agreement and this Agreement, the stipulations and provisions in this Agreement shall prevail. Seller shall have the right to audit Purchaser’s systems with respect to handling adverse event reporting in connection with the Products, any such audit to be done during normal business hours on reasonable notice, and in a fashion to avoid unnecessary disruption to normal business operations. Any complaint or adverse event received by one party that relates to product manufacture or packaging must be reported to the other party within 3 business days. The Pharmacovigilence Agreement shall set forth additional details with respect to the handling of adverse event reporting. In order to ensure compliance with safety reporting requirements in the respective Territories the parties shall agree on a process and procedure for sharing adverse event information which shall be documented in a Pharmacovigilance Agreement (the “Pharmacovigilence Agreement”). Within thirty (30) days from the effective date of this Agreement each party shall assign a safety representative to begin discussions to ensure a Pharmacovigilence Agreement is executed no later than April 1, 2011. Pending execution of such agreement, the parties shall, as required, within thirty (30) days implement an interim procedure fo...
Reporting etc. Purchaser shall have the responsibility in the Territory for complying with all regulatory filings, reporting requirements and other matters which relate solely to Purchaser’s acting as a distributor of the Product in the Territory. All other regulatory reporting matters (including adverse event and Product complaint reporting) shall be Seller’s responsibility. Each of Seller and Purchaser shall notify the other of receipt of any report(s) of adverse events or product complaints pursuant to Exhibit C. Exhibit C sets forth additional details with respect to the handling of adverse event reporting.
Reporting etc. As soon as practicable but in any event no later than the 25th day of each calendar month, the Collection Agent will deliver to the Servicing Agent
