Xxxxxx Responsibilities. During the Research Program Term, Xxxxxx will (a) use Commercially Reasonable Efforts to conduct the Xxxxxx Research Activities assigned to it in each Research Plan and (b) commit such other resources as are reasonably necessary to conduct such Xxxxxx Research Activities and achieve the goals of the Research Program.
Xxxxxx Responsibilities. Xx. Xxxxxx shall ensure that the IRO has access to all records and personnel necessary to complete the reviews listed in Section III.C of this IA and that all records furnished to the IRO are accurate and complete.
Xxxxxx Responsibilities. X. Xxxxxx shall be responsible for the assignment of Students to the Field Site. Xxxxxx agrees to refer to the Field Site only those Students who have completed the prerequisite course of study as determined by Xxxxxx.
X. Xxxxxx shall provide a field education coordinator (the "Xxxxxx Coordinator") who will act as a liaison between Xxxxxx and the Field Site and coordinate the Field Experience Program with the Field Site. The Xxxxxx Coordinator will be responsible for maintaining communication with the Field Site including, but not limited to:
(1) Confirming any contact information for Students to the Field Site Coordinator, as defined below, prior to the Student assignment; and
(2) Supplying the Field Site with information regarding each Student’s current level of academic preparation as may be required by the Field Site.
X. Xxxxxx shall provide an instructor (the “Xxxxxx Supervisor") who will serve as the academic course instructor and field experience instructor for the educational experience. The Xxxxxx Supervisor will have responsibilities including, but not limited to:
(1) Communicating with the Field Site Supervisor relating to each Student’s educational experience at the Field Site;
(2) Evaluating student academic and Field Site work relating to the educational experience at the Field Site.
X. Xxxxxx shall provide the Field Site with information regarding the particular requirements relating to Field Experience Programs including required hours and supervision requirements.
X. Xxxxxx maintains student professional liability insurance with One Million Dollars ($1,000,000) per occurrence/claim and Three Million Dollars ($3,000,000) annual aggregate. Xxxxxx shall provide the Field Site with proof of coverage upon request.
Xxxxxx Responsibilities. Remittances and Settlement
Xxxxxx Responsibilities. 1. Lessor shall render decisions and approvals required by the Lease or this Exhibit “C” relating to design and construction in a timely manner and in accordance with BREP’s schedule agreed to by Lessor.
Xxxxxx Responsibilities. Genova shall ensure that the IRO has access to all records and personnel necessary to complete the reviews listed in III.D of this CIA and that all records furnished to the IRO are accurate and complete.
Xxxxxx Responsibilities. Tesla agrees to repair or replace any covered part as required due to a Failure. For additional information see Section I.
Xxxxxx Responsibilities. XXXXXX shall use commercially reasonable efforts during the Term to (i) conduct the Services in accordance with each Statement of Work and (ii) provide to MRK the Reports (as defined below).
Xxxxxx Responsibilities. 1. Display a sign stating that the Farmer is authorized to redeem WIC cash value fruit and vegetable benefits and WVFMNP benefits.
2. Accept checks and electronic food benefits of the respective programs for which the farmer is authorized. Benefits will only be accepted from eligible participants, parents/caretakers of infant and child participants, or proxies.
3. Provide eligible fruits and vegetables at the same quality and current price or less than current price charged to other customers.
4. Assure that benefit check and electronic benefit transactions are only for eligible foods.
5. Keep all information of authorized WIC/FMNP shoppers confidential.
6. Accept training on check and electronic benefits procedures and provide training to all employees on such procedures.
7. Provide such information as the participating Nutrition Services Programs may require for periodic reports to USDA Food and Nutrition Service.
8. Agree to be monitored for compliance with the West Virginia WIC program requirements, including both overt and covert monitoring.
9. Be accountable for actions of Xxxxxx’x employees in the provision of authorized foods and related activities.
10. Reimburse the West Virginia WIC Program for any checks/electronic benefits transacted in violation of this Agreement.
11. Offer eligible participants, parents, caretakers of child participants, and proxies the same courtesies as other customers. Ensure participants are not required to use special checkout areas that are not used by other customers.
12. Comply with the non-discrimination provisions of USDA regulations as provided in 7 CFR §248.7,§248.10(a)(6), §247.7, §249.10(a)(9).
13. Notify the West Virginia WIC Program if any Farmers’ Market or Farm Stand ceases operation prior to the end of the authorization period and of any address changes or corrections.
14. Agree to actually grow at least one type of fruit or vegetable offered for sale. The Farmer cannot participate if all fruits and vegetables that are sold were purchased from a third party.
15. Agree that all fruits and vegetables sold shall be grown in West Virginia or within 50 miles of the West Virginia border.
16. Agree to not collect sales tax on eligible purchases.
17. Ensure that participants, parents, caretakers or infant and child participants or proxies are not required to purchase the full amount on a check or an electronic benefit.
18. Agree to not seek restitution from eligible participants, parents, caretakers of child partic...
Xxxxxx Responsibilities. Xxxxxx shall; and, as applicable, shall require any Subcontractor to;
A. Appropriately register its manufacturing establishments with the FDA and other regulatory agencies as required;
B. Maintain required ISO and EN certification for each Manufacturing Facility, and comply with all EU and other applicable foreign regulatory requirements.
C. Comply with the QSR requirements and other relevant regulations issued by the FDA, state, local or other regulatory agencies and in effect from time to time, except to the extent that a QSR or other regulatory obligation has been allocated to Newco under the Agreements between Newco and Xxxxxx.
D. When practicable, permit Newco to send a representative to attend, or when such attendance is not permitted or practicable, provide Newco with periodic progress reports on every visit to a relevant Manufacturing Facility by the FDA or other regulatory agency which affects or concerns the manufacture of the Antibodies Reagents or Reagent Kits (such reports to be given as frequently as reasonably possible, but not more often than once in each 24-hour period, during that portion of the visit which directly affects or concerns any Antibody, Reagent or Reagent Kit). Newco shall be provided with a copy of any Form FDA-483, Establishment Inspection Report (EIR and/or Warning or "untitled" Letter generated as a result of an FDA visit, or any equivalent foreign, state or local document generated as a result of an inspectional visit, and responses thereto (which copies may be redacted to the extent necessary to protect confidential information unrelated to the Antibodies, Reagents or Reagent Kits, provided that such redaction does not prevent Newco from -------- discerning any information that is related to the Antibodies, Reagents or Reagent Kits. Newco shall also be apprised as soon as possible of the time and place of any "close out" meeting at the end of an FDA or other agency visit and be allowed to attend the meeting when the meeting directly affects or concerns any Antibody, Reagent or Reagent Kit, provided that, in -------- the discretion of Xxxxxx'x or its Subcontractor's regulatory professionals, the presence of a Newco representative would not prejudice Xxxxxx'x or its Subcontractor's interests.
E. Respond, in a timely manner, after consultation with Newco, to any Form FDA-483, Warning or "untitled" Letter or Section 305 Notice received, and any other notices or letters received from the FDA, a state or local regulatory auth...
