Required Reporting Frequency Sample Clauses

Required Reporting Frequency. Daily Required Reporting Method or Venue: Web-portal File Type: csv De-limiting character: “,” comma with values enclosed by Quotation Marks Subject to compliance with the applicable provisions of HIPAA, the Care Coordination Reports should adhere to the following format & should not-deviate in order from one report to the next: Status Patient Referral MFG Acct # Date Rec. Contact Date Touch Date Comments F/U Date Ship Date Cancel Date Ins Name Phys Name Phys City Phys State Phys Zip Phys Phone Patient Address Patient City Patient State Patient Zip Patient Phone Patient DOB Serial No. Part No. Quantity
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Required Reporting Frequency. Daily Required Reporting Method or Venue: Web-portal File Type: csv De-limiting character: “,” comma with values enclosed by Quotation Marks Subject to compliance with the applicable provisions of HIPAA, the Care Coordination Reports should adhere to the following format & should not-deviate in order from one report to the next: Status Patient Referral MFG Acct # Date Rec. Contact Date Touch Date Comments F/U Date Ship Date Cancel Date Ins Name Phys Name Phys City Phys State Phys Zip Phys Phone Xxxxxxx Xxxxxxx Xxxxxxx Xxxx Patient State Patient Zip Patient Phone Patient DOB Serial No. Part No. Quantity
Required Reporting Frequency. Daily Format: .csv (comma-delimited file) Delivery Method: Dexcom controlled secure file transfer protocol site specific to Distributor Dexcom, Inc. Sales Tracings Requirements Field Format Desired State Comments Dexcom drop ship info included Text No Frequency Text Daily Format Text CSV Delivery method Text sftp Customer ID Number Text Unique identifier A unique identifying number for each customer Customer First Name Text Separate field for first Customer Last Name Text Separate field for last Customer Xxxxxx Xxxxxxx Xxxx Xxxxxxxx Xxxxxx Xxxxxxx Customer City Text Customer City Customer State Text Customer State Customer ZIP Code Text Customer ZIP Code 5-character; text so leading zeros are included; no Zip + 4 numbers Customer DOB Text Customer DOB MM/DD/YYYY Customer Phone Text Text Customer Email Text Text Physician First Name Text Separate field for first Physician Last Name Text Separate field for last Physician Xxxxxx Xxxxxxx Xxxx Xxxxxxxxx Xxxxxx Xxxxxxx Physician City Text Physician City Physician State Text Physician State Physician ZIP Code Text Physician ZIP Code 5-character; text so leading zeros are included; no Zip + 4 numbers Physician NPI Text Physician NPI Medical Facility Name Text Medical Facility Name Medical Facility Xxxxxx Xxxxxxx Xxxx Xxxxxxx Xxxxxxxx Xxxxxx Xxxxxxx Medical Facility City Text Medical Facility City Medical Facility State Text Medical Facility State Medical Facility ZIP Code Text Medical Facility ZIP Code Insurance Name Text Insurance Name Item Number Text Item Number Quantity Text Quantity Unit quantity - e.g. 1 box of sensors is '1', and not the number of individual sensors included Benefit Type Text Benefit Type DME or Pharmacy H/W Lot Number H/W Lot Number Where distributor stocks and ships hardware H/W Serial Number H/W Serial Number Where distributor stocks and ships hardware Date of Sale Date of Sale MM/DD/YYYY Shipper Dexcom or distributor name Dexcom or Distributor, where distributor provides tracings including shipments from both locations 5. SCHEDULE 5. Schedule 5 is amended and restated in its entirety as follows: SCHEDULE 5

Related to Required Reporting Frequency

  • Required Reports (1) As required in Attachment H, Disadvantaged Business Enterprise or Historically Underutilized Business Program Requirements, the Engineer shall submit Progress Assessment Reports to report actual payments made to Disadvantaged Business Enterprises or Historically Underutilized Businesses. One copy shall be submitted with each billing statement and one copy shall be submitted to the address included in Attachment H, Disadvantaged Business Enterprise or Historically Underutilized Business Program Requirements.

  • Adverse Event Reporting Both Parties acknowledge the obligation to comply with the Protocol and / or applicable regulations governing the collection and reporting of adverse events of which they may become aware during the course of the Clinical Trial. Both Parties agree to fulfil and ensure that their Agents fulfil regulatory requirements with respect to the reporting of adverse events.

  • Additional Reporting Requirements Contractor agrees to submit written quarterly reports to H-GAC detailing all transactions during the previous three (3) month period. Reports must include, but are not limited, to the following information:

  • Reporting Compliance The Company is subject to, and is in compliance in all material respects with, the reporting requirements of Section 13 and Section 15(d), as applicable, of the Exchange Act.

  • Commission Reporting (a) The Trust Administrator, each Servicer and the Master Servicer shall reasonably cooperate with the Depositor in connection with the Trust’s satisfying the reporting requirements under the Exchange Act. The Trust Administrator shall prepare on behalf of the Depositor any Forms 8-K and 10-K customary for similar securities as required by the Exchange Act and the rules and regulations of the Commission thereunder, and the Depositor shall sign and the Trust Administrator shall file (via XXXXX) such Forms on behalf of the Depositor. The Depositor hereby grants to the Trust Administrator a limited power of attorney to execute and file each such document on behalf of the Depositor. Such power of attorney shall continue until the earlier of (i) receipt by the Trust Administrator from the Depositor of written termination of such power of attorney and (ii) the termination of the Trust.

  • Reporting Requirements The Company, during the period when the Prospectus is required to be delivered under the 1933 Act or the 1934 Act, will file all documents required to be filed with the Commission pursuant to the 1934 Act within the time periods required by the 1934 Act and the 1934 Act Regulations.

  • Information and Reporting Requirements 63 7.1 Financial and Business Information.........................................................63 7.2

  • Reporting Covenant Required Complies Monthly financial statements with Compliance Certificate Monthly within 30 days Yes No Annual financial statement (CPA Audited) + XX XXX within 180 days Yes No A/R & A/P Agings Monthly within 30 days Yes No Deferred Revenue (if applicable) Monthly within 30 days Yes No Borrowing Base Certificate (if Borrowing Base Eligible and any Advances are outstanding) Monthly within 30 days Yes No Board Projections FYE within 30 days of Board Approval Yes No Performance Pricing Net Cash Applicable Rate Applies Borrowing Base Eligible Net Cash ³ $15,000,000* WSJ Prime + 0.35% Yes No Yes Net Cash < $15,000,000* WSJ Prime + 1.75% Yes No No Non-Formula Loans Net Cash Non-Formula Applicable Rate Applies Non-Formula Loan Eligible Net Cash ³ $15,000,000 WSJ Prime + 1.25% Yes No Yes Net Cash < $15,000,000 WSJ Prime + 1.25% Yes No No Financial Covenant Required Actual Compliance Adjusted Quick Ratio (monthly)* 1.25:1.00 :1.00 Yes No Net Cash* $15,000,000 $ Yes No Unrestricted Cash and Cash Equivalents at Bank and Bank Affiliates** $25,000,000 $ Yes No * Commencing with the month ending November 30, 2017 ** Through October 31, 2017 The following financial covenant analysis and other information set forth in Schedule 1 attached hereto are true and accurate as of the date of this Certificate. All other representations and warranties in this Agreement are true and correct in all material respects on this date, and Borrower represents that there is no existing Event of Default. Sincerely, TINTRI, INC. Signature Title Date

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