Process Documentation. Supplier processes that can affect product quality shall be documented and followed. This documentation shall also be available for auditing.
Process Documentation. The provider's and also sub-contractor’s manufacturing process should be validated and documented.
Process Documentation. These services shall include:
Process Documentation. Printed material relating to the Process and instructions for its use, as more fully described in the specifications contained in Exhibit B, supplied herewith under separate cover, Documentation is classified as Development Documentation and Production Documentation, as defined herein below.
Process Documentation the lender must provide documentation on for each unique E-Sign process used to execute Loans in the portfolio. If the lender, or its origination servicer, used more than one process, or if the process has been modified since the oldest E-Signed Loan in the portfolio was executed, then each process must be documented. Process documentation must contain the following, in addition to any other materials reasonably requested by the Borrower or the holder:
Process Documentation. Scios shall be responsible for obtaining all necessary Regulatory Approval for the clinical testing, marketing and sale of Product. Abbott agrees to provide to Scios all information necessary for Scios to prepare the Chemistry Manufacturing and Controls Section of Scios' NDA for the Product. Abbott presently has a single Type 1 Drug Master File #2869 on file with the FDA. Abbott shall make available to Scios for inspection and copying (at reasonable times and upon reasonable notice to Abbott) any of the procedures and methods listed in Exhibit B as the same may be amended from time to time and shall, upon Scios' written request, send a letter to the FDA authorizing FDA to reference any appropriate Drug Master File on behalf of the Scios application, as might be necessary for Scios' filings with the FDA or to obtain NDA approval from the FDA based on Xxxxxx'x participation as formulator and manufacturer of the Product as contemplated by this Agreement. Abbott shall also provide such other assistance (including granting Scios the right to reference any of Xxxxxx'x Drug Master Files if additional filings are made by Abbott) as Abbott can reasonably provide to ***** Confidential portions of this material have been omitted and filed separately with the Securities and Exchange Commission. support Scios' efforts to obtain Regulatory Approval for Fill and Finish Work of Product by Abbott.
Process Documentation. Scios shall be responsible for obtaining all necessary Regulatory Approval for the clinical testing, marketing and sale of Product. Abbott agrees to provide to Scios all information necessary for Scios to prepare the Chemistry Manufacturing and Controls Section of Scios’ NDA for the Product. Abbott presently has a single Type 1 Drug Master File #2869 on file with the FDA. Abbott shall make available to Scios for inspection and copying (at reasonable times and upon reasonable notice to Abbott) any of the procedures and methods listed in Exhibit B as the same may be amended from time to time and shall, upon Scios’ written request, send a letter to the FDA authorizing FDA to reference any appropriate ***** Confidential portions of this material have been omitted and filed separately with the Securities and Exchange Commission.
Process Documentation. 4.9.2.1 Manufacturing Documentation for manufacturing shall be provided my HighwayMaster's contract manufactures. Documents should include the following types"
Process Documentation. Supplier shall develop, and IdentifySensors shall approve, the following:
Process Documentation. Supplier has provided to Customer certain documentation of end to end processes for the Services (the “Process Documentation”). Supplier shall maintain the Process Documentation on a reasonably current basis to reflect the end to end processes then being used to provide the Services. Without limiting the foregoing, reasonably promptly following any termination of this Agreement or any individual Service, Supplier shall update all of the Process Documentation or the Process Documentation for the terminated Service, respectively, and provide it to Customer.
