Event Reporting Sample Clauses

Event Reporting. Upon the completion of the Event and at the request of the Commission, User will provide to the Commission, for reporting purposes the following information; the number of teams that participated in the Event, the number of participants per team, the age of each participant, the gender of each participant, the zip code of each participant and the number of games played by each team.

Event Reporting. The Contractor must ensure the Aircraft are equipped with event reporting equipment to meet the engine and flight event reporting requirements of the NAFC Standard OPS- 014 Aircraft Tracking, Event Reporting and Messaging.

Event Reporting. The ACA must receive reports on all insured Affiliate Organization activities to provide insurance coverage to all participants and to keep insurance costs to minimum. Therefore, the Affiliate and its activity leaders agree to submit reports for their insured activities to the ACA, in accordance with the requirements listed below:

Event Reporting. The ACA must receive reports on all insured PAC activities which include non-ACA members for the protection of the club and all participants. Therefore, the PAC and its activity leaders agree to submit reports for their insured activities which include non-ACA members to the ACA via online form submission only, in accordance with the requirements listed below: a. Activities with no non-ACA members: For activities in which all participants are current ACA members, the PAC does not need to submit an event final report. However, the PAC must ensure that all ACA members have signed a waiver prior to participating in the activity.

Event Reporting i. Flight Crew Members shall notify the Flight Operations Department of a Safety Event within 48 hours of first becoming aware of the event taking place. Notification may be by phone, e-mail or fax. In addition, each Flight Crew Member shall submit a written report, in a form agreed to by the parties, at the earliest opportunity, but no later than seven days after first reporting the Safety Event. ii. When a Flight Crew Member submits a report concerning a Safety Event and thereby seeks immunity from discipline in connection with the event, his (her) report shall be De-identified by the Flight Safety Officer and forwarded to the Event Review Committee. iii. When a third party submits a report concerning a Safety Event involving a flight crew member, the Flight Safety Officer will invite the Flight Crew Member to submit his (her) own report on the event.

Event Reporting. Each Party shall be responsible for reporting all Events (as defined below) associated with the Development or Commercialization of Licensed Product in its respective territory (as to GSL, the Territory and, as to Lipocine, outside the Territory) to the appropriate Regulatory Authorities in its respective territory, in accordance with all Applicable Laws, and shall provide the other Party copies of all such reports promptly after filing with the Regulatory Authorities. Additionally, in the event either Party receives information regarding Events related to the use of Licensed Product, such Party shall promptly provide the other Party with such information in accordance with the separate Safety Agreement to be entered into by the Parties promptly. For purposes of this Section 3.6, “Event” shall mean any Licensed Product complaint, adverse event or adverse drug reaction, including malfunctions, product failure, improper or inadequate design, manufacturer labeling, quality control or user error reported during the use of the Licensed Product by or on behalf of a Party, its Affiliates, Sublicensees and customers (including end users purchasing Licensed Product or using Licensed Product purchased from any of the foregoing). Each Party shall notify the other Party immediately of any Information received regarding any threatened or pending action by any public authority that may affect or related to the safety, efficacy, or other labeling claims of any Licensed Product. Without limiting the foregoing, the Parties shall negotiate in good faith and enter into a pharmacovigilance agreement consistent with this Section 3.6.

Event Reporting. (a) 5.2 When providing the Services, once the scene is secure, Contractor shall report all events immediately to PREPA. Following initial notification, standardized incident reports shall be completed and submitted to LUMA 's HSEQ Department. An initial written report shall be submitted by 8:00 am the following day. Within 5 days, Contractor shall submit an in-depth written report. All environmental spills must be reported immediately to PREPA as appropriate.

Event Reporting. Flex offers the following reports available through the User Interface to quantify program performance. Any exportable data not available via the user interface will not be provided on an on-going basis. ● An event performance report that shows the measurement and verification results for all events in the season. o Subject to complete meter data o Final reports available within 30 days of the end of the operational season ● A notification report that shows the status of notification delivery. o Available after event completion ● An enrollment report that shows enrollment data for a specified period.

Event Reporting a) FCMs shall notify the Flight Operations Department of a Safety Event within 48 hours of first becoming aware of the event taking place. Notification may be by phone, e-mail or fax. In addition, each FCM shall submit a written report, in a form agreed to by the parties, at the earliest opportunity, but no later than seven days after first reporting the Safety Event. b) When a FCM submits a report concerning a Safety Event and thereby seeks immunity from discipline in connection with the event, his report shall be de- identified by the Manager, Flight Safety and forwarded to the Event Review Committee. c) When a third party submits a report concerning a Safety Event involving a FCM, the Manager, Flight Safety will invite the FCM to submit his own report on the event.

Event Reporting. If SELLER receives a complaint from any Third Party, or if SELLER’s quality assurance group, infant formula business unit managers, or senior management otherwise become aware of a complaint or issue, about Martek Product involving safety concerns, SELLER shall promptly notify PURCHASER in writing. In addition, during the Term of this Agreement, PURCHASER shall promptly notify SELLER of any report of an adverse event once it has determined that it is potentially associated with the use of Martek Products in any Wyeth Product or Growing Up Milk Product, and SELLER shall notify PURCHASER of any report of an adverse event received by SELLER regarding a Wyeth Product or Growing Up Milk Product irrespective of whether the adverse event is potentially associated with the use of a Martek Product. All adverse event notifications as stated above shall occur within five (5) calendar days of receipt of a report of such adverse event. PURCHASER shall have sole discretion in determining what action, if any, is to be taken by PURCHASER in connection with any such adverse event relating to a Wyeth Product or Growing Up Milk Product. The Parties shall be notified as follows (or in such other manner as provided by notice pursuant to Section 11.4): For SELLER: Fax number: (000) 000-0000 Mr. Xxxxx Xxxxxx Regulatory Manager Martek Biosciences Corporation 0000 Xxxxxx Xxxx Columbia, MD 21045 (tel) 000-000-0000 For PURCHASER: Fax number: (000) 000-0000 Overnight Courier (only): Global Safety Surveillance Epidemiology & Labeling Wyeth Research GSSEL Triage Unit Dock E 000 Xxxxxx Xxxx Xxxxxxxxxxxx, XX 00000 * The asterisk denotes that confidential portions of this exhibit have been omitted in reliance on Rule 24b-2 of the Securities Exchange Act of 1934. The confidential portions have been submitted separately to the Securities and Exchange Commission.