Which Is The Electronic Equivalent Of A User Manual
The Dataset can be defined as the electronic equivalent of the cover page for the sampling and analytical results that are submitted to the SRP via hard copy. The DATASET file provides basic information about the sampling event, including site description, investigation phase, consultant, submittal date, and other information. There should be only one record in each Dataset file. The Dataset may represent one or more sampling episodes at a site. For example, the sampling and analytical results of four rounds of quarterly monitoring (at the same site) can be submitted as a single dataset.
Which Is The Electronic Equivalent Of A User Manual
The ICE Model, which is the electronic version of the "Model Incurred Cost Proposal" provides contractors with a standard, user-friendly ICE submission package for preparing adequate incurred cost proposals in accordance with FAR 52.216-7, "Allowable Cost and Payment" (see note 1 below). To assist contractors in meeting this requirement, this web page provides Version 2.0.1h (released April 2018) of DCAA's electronic model incurred cost proposal.
The intent of this user manual is to provide guidance on the procedures to be followed to successfully create, upload, verify, and submit the monthly CEM data to Alberta Environment and Parks and the Alberta Energy Regulator.
Two example Project Data Sets are available for use as examples of comprehensive data entry and documentation. The file Method 29-30B Example Data 2014 (zip) contains a populated Project Data Set example of single and paired train manual test methods. A second Project Data Set which is unpopulated is provided for users to test the importing of field data. Included in the ZIP file are two spreadsheet files and two XML files for use in demonstrating importing the point and header field data. The file RATA DATA Demo 08-27-2012 (zip) contains a populated Project Data Set example of instrumental test methods and the performance specifications for those test methods. Updated October 2014.
The ERT has the ability to import stack test data for manual test methods from either a specially formatted spreadsheet or from an XML file complying with an established Schema (available through a link in the next paragraph). We have prepared four properly formatted spreadsheet templates which companies may use to import data into the ERT. These are intended to reduce the effort associated with field data entry into the ERT and improve the reliability of data transcription. The document, Requirements for modifying a spreadsheet for ERT import (3 pp, 25 K, About PDF), describes how to merge the ERT point and header data spreadsheet template with a proprietary corporate field data spreadsheet so you can use the import function into the ERT.The Isokinetic and manual methods import sheet (3. above) includes instructions for importing the common point and header data when a single sample train is used for each test run. The Method 30B import template (2. above) is a spreadsheet that includes instructions for importing similar data when dual sample trains are used for each test run. We also have two XML Schema for ERT field data which are alternatives to the spreadsheet templates. Equipment vendors would be the most likely users of the Schema to program their equipment to generate XML files that the ERT can import. The Schema ERT Single Sampler Manual Method XML Schema (XSD) (xsd) is used to describe the format of an export file for single sample train equipment.
The NUCC has developed a 1500 Reference Instruction Manual detailing how to complete the claim form. The purpose of this manual is to help standardize nationally the manner in which the form is being completed.
The Medical Device Reporting (MDR) regulation (21 CFR Part 803) contains mandatory requirements for manufacturers, importers, and device user facilities to report certain device-related adverse events and product problems to the FDA. The regulation specified that reports be filed on the FDA's Medwatch Form 3500A or an electronic equivalent. The FDA published a final rule on Feb. 14, 2014, requiring manufacturers and importers to submit MDRs to the FDA in an electronic format that the FDA can process, review, and archive. This rule will be effective as of Aug.14, 2015.
Please note that 803.30 (which addresses User Facility Reporting Requirements) does NOT state that device user facilities are required to report device malfunctions where the malfunction would likely cause or contribute to death or serious injury if the malfunction were to recur.
(a) The regulations in this part set forth the criteria under which the agency considers electronic records, electronic signatures, and handwritten signatures executed to electronic records to be trustworthy, reliable, and generally equivalent to paper records and handwritten signatures executed on paper.
(c) Where electronic signatures and their associated electronic records meet the requirements of this part, the agency will consider the electronic signatures to be equivalent to full handwritten signatures, initials, and other general signings as required by agency regulations, unless specifically excepted by regulation(s) effective on or after August 20, 1997.
(2) The document or parts of a document to be submitted have been identified in public docket No. 92S-0251 as being the type of submission the agency accepts in electronic form. This docket will identify specifically what types of documents or parts of documents are acceptable for submission in electronic form without paper records and the agency receiving unit(s) (e.g., specific center, office, division, branch) to which such submissions may be made. Documents to agency receiving unit(s) not specified in the public docket will not be considered as official if they are submitted in electronic form; paper forms of such documents will be considered as official and must accompany any electronic records. Persons are expected to consult with the intended agency receiving unit for details on how (e.g., method of transmission, media, file formats, and technical protocols) and whether to proceed with the electronic submission.
(c) Persons using electronic signatures shall, prior to or at the time of such use, certify to the agency that the electronic signatures in their system, used on or after August 20, 1997, are intended to be the legally binding equivalent of traditional handwritten signatures.
(2) Persons using electronic signatures shall, upon agency request, provide additional certification or testimony that a specific electronic signature is the legally binding equivalent of the signer's handwritten signature.
EDP performs a series of formatting checks on the EDD and identifies a select group of errors in the data file prior to submission. Recent Version 4 EDD format changes have incorporated most of the checks that data providers were completing manually formerly contained in the Final Checklist for Submission of EDDs (PDF) (1.3 MB) to DEC. This should streamline the process of preparing, reviewing, and finalizing EDD submissions to NYSDEC now that these error checks are part of the EDD format files. You will need to register the EDP software with EarthSoft (this is free), instructions on this are located in the EDP Quickstart Guide (PDF). You will typically receive an email within 2 business days from the NYSDEC EIMS Administrator confirming the software registration and providing a user login id and password to submit the checked EDD. If you do not receive a confirmation email within 2 days, please do not attempt to reregister, contact the NYSDEC EIMS Administrator at NYENVDATA@dec.ny.gov.
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The documents supplied with your bike provide useful info about your Ducati: from the colour code to the specifications of some electronic and mechanical components, all the way to details about the main service interventions. You may download a digital version of your owner's manual, but remember to contact Ducati Service at all time to service your motorcycle.