REVIEW COMPLIANCE Sample Clauses

REVIEW COMPLIANCE. The Recipient agrees that Western will have the right, at any time, to monitor, audit, and review activities and methods in implementing this DSA in order to assure compliance therewith, within the limits of Recipient’s technical capabilities.
Sample 1
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REVIEW COMPLIANCE. Each office will have a BUYER designee to monitor compliance with the politics. . BUYER employees will also be required to comply with the BUYER's confidentiality policies and procedures, and the BUYER's Code of Conduct. . Failure to comply will be sufficient cause for (but will not require in all cases) disciplinary action, including termination of employment and possible legal action. In conclusion, BUYER believes these steps will ensure that non-public client information remains confidential.
Sample 1
REVIEW COMPLIANCE. The Lead Consultant or consultant in the requisite professional discipline will certify that the Contract Documents, prepared under its direction, are in full compliance with applicable codes, regulations, and condition set forth by the governing regulatory agencies at the time of advertisement and monitor for changes that impact the project schedule or cost. The Lead Consultant will be responsible for thoroughly reviewing the Contract Documents and checking for constructability, i.e. clearances, material availability and guaranteed delivery dates at the time of advertisement.
Sample 1

Related to REVIEW COMPLIANCE

  • FDA Compliance The Company: (A) is and at all times has been in material compliance with all statutes, rules or regulations of the FDA and other comparable governmental entities applicable to the ownership, testing, development, manufacture, packaging, processing, use, distribution, marketing, labeling, promotion, sale, offer for sale, storage, import, export or disposal of any product under development, manufactured or distributed by the Company (“Applicable Laws”); (B) has not received any FDA Form 483, notice of adverse finding, warning letter, untitled letter or other correspondence or notice from the FDA or any governmental entity alleging or asserting material noncompliance with any Applicable Laws or any licenses, certificates, approvals, clearances, exemptions, authorizations, permits and supplements or amendments thereto required by any such Applicable Laws (“Authorizations”); (C) possesses all material Authorizations and such Authorizations are valid and in full force and effect and the Company is not in material violation of any term of any such Authorizations; (D) has not received notice of any claim, action, suit, proceeding, hearing, enforcement, investigation, arbitration or other action from the FDA or any governmental entity or third party alleging that any product operation or activity is in material violation of any Applicable Laws or Authorizations and has no knowledge that the FDA or any governmental entity or third party is considering any such claim, litigation, arbitration, action, suit, investigation or proceeding; (E) has not received notice that the FDA or any governmental entity has taken, is taking or intends to take action to limit, suspend, modify or revoke any material Authorizations and has no knowledge that the FDA or any governmental entity is considering such action; and (F) has filed, obtained, maintained or submitted all material reports, documents, forms, notices, applications, records, claims, submissions and supplements or amendments as required by any Applicable Laws or Authorizations and that all such reports, documents, forms, notices, applications, records, claims, submissions and supplements or amendments were materially complete and correct on the date filed (or were corrected or supplemented by a subsequent submission).

  • Regulatory Compliance a. Monitor compliance with the 1940 Act requirements, including:

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