Conditions of Supply. 9.3.1.1 An employee, when working on site, is required to wear all footwear and clothing supplied.
Conditions of Supply. Turnkey Workflows and Precedent Documents Our Turnkey workflows are designed to enable you to get your case management off to a flying start by giving you a suite of dossier fields and pages, precedent letter templates, and workflows across a number of areas of legal work. The areas of law available at present are as detailed below, and we are currently working to increase the range offered. The Turnkey workflows do provide a fully automated process for your case management, but are not a fully customised case management configuration. Training on editing the precedent documents, workflows etc, and creating new precedents is included within the basic package to enable you to fine tune the case management to meet your specific requirements. In view of the highly automated and complex nature of the Turnkey case management, we would stress the importance of your chosen trainee(s) being fully conversant with Word functionality. While we endeavour to ensure that the content is as up to date as possible, Pracctice Limited and our partner companies can take no responsibility for the legal content of the precedent documents supplied as part of a workflow package. Turnkey case management can only be used with the standard set of worktypes developed by Pracctice Limited and cannot be imported onto your existing worktypes. CASE MANAGEMENT OPTIONS Case Management Custom Built Package A case management bespoke package consists of one on site specification day, three off site development days and two on line training sessions. During the morning of the on site specification day a member of our training team will demonstrate and discuss the functionality offered by OspreyTM that you can use in your case management package. During the afternoon we shall help you build your case management system using our standard forms. Once you have completed these they will then be submitted to Pracctice so that the 3 days of development can begin. You are limited to providing us with 75 standard letters/forms (each day we expect to create 25 letters) however you may purchase additional case management development days should your requirement exceed this. Whilst we would encourage you to make full use of all of the case management functionalities within OspreyTM you may only choose to use certain facilities such as dossier pages, keydates or standard letters initially. You can of course decide to start by using the basics of the system and then build on your use of the application as y...
Conditions of Supply. Full Rights This document is supplied in confidence to MOD in accordance with Contract No [ABC/1234, task XYZ/9876]. (see note 1) The document comprises information proprietary to [Rights Owner] and whose unauthorised disclosure may cause damage to the interests of [Rights Owner]. (see note 2) The document is supplied to MOD as a FULL RIGHTS VERSION under the terms of DEFCON 705 (Edn 11/02) and, except with the prior written permission of [Rights Owner], MOD’s rights of use and dissemination in the document are limited to those set out in that Condition and the Contract for the use of Full Rights Versions of Technical Deliverables. Requests for permission for wider use or dissemination should be made to the relevant [Rights Owner] Account Manager. Conditions Of Supply – Limited Rights This document is supplied in confidence to MOD in accordance with Contract No [ABC/1234, task XYZ/9876]. (see note 1) The document comprises information proprietary to [Rights Owner] and whose unauthorised disclosure may cause damage to the interests of [Rights Owner]. (see note 2) The document is supplied to MOD as a LIMITED RIGHTS VERSION under the terms of DEFCON 705 (Edn 11/02) and, except with the prior written permission of [Rights Owner], MOD’s rights of dissemination of the document are limited to UK government departments and to service providers under the terms of Clause 14 of DEFCON 705. Requests for permission for wider use or dissemination should be made to the relevant [Rights Owner] Account Manager. (see note 3) Notes:
Conditions of Supply. General conditions GDF procures only quality assured medicines. All medicines and commodities shall be provided to patients free of charge. Standard production lead times are 4-6 months after receipt of funds. No approval from Green Light Committee, either global or regional, is needed. However, GDF may provide a copy of this document to the responsible regional or global Green Light Committee(s) for their advice; this is particularly relevant for Global Fund supported procurements. Procurement processes WHO/GDF works with procurement agent(s) (PA) to coordinate the purchasing and logistics of WHO/GDF order(s) under this MPTA (MDR-TB Procurement Request Form and Technical Agreement). The execution of this MPTA can be initiated only after signing of a commercial contract between the PA and the Client and receipt of the prepayment of funds by PA, or as agreed in writing between the PA and the Client. The Client will be responsible for payment or obtaining waiver of any applicable duties, any import requirements, as well as to facilitate product registration in cooperation with manufacturers or obtaining relevant waivers, in-country storage, distribution and monitoring of all supplies, unless otherwise agreed with the PA and/or WHO/GDF The Client understands the importance of quality medicines. Applicants submitting a MPTA for partial regimens understand that it is their direct responsibility to ensure that other medicines provided are of assured quality and they are fully accountable for the care of their patients. In the case of Global Fund supported procurements, prior written agreement of the Global Fund is required if the funds are to support partial regimens. Monitoring and technical assistance WHO/GDF reserves the right to conduct monitoring mission(s) by an independent technical agency on the use of medicines and related commodities delivered under this document. The Client agrees to interact with experts which WHO/GDF may notify and from which WHO/GDF may request assessments, such as but not limited to WHO Regional TB Advisors, regional Green Light Committee (rGLC) representatives, WHO Regional Supply Officers and Country Supply Officers. The assessment report will be shared with the Client. The Parties may also consult on and mutually agree on implementation of technical assistance on MDR-TB medicines management. Special provisions Any serious adverse effects that come to the Client’s attention and that may be related to the use of the medicines are...
Conditions of Supply. 2.1 The Contractor represents, warrants and agrees that it and its Personnel will:
Conditions of Supply. 5.1 Unless otherwise agreed in relation with a specific project the following terms and conditions shall be applicable to all orders for the purchase of the Products (or portion thereof) to be supplied by P-COM to Siemens and such terms and conditions shall take preference over any conflicting or inconsistent terms of Siemens' purchase orders or P-COM conditions of sale.
Conditions of Supply. Before we arrange for the supply of Energy to your Site, and before this Energy Agreement comes into effect:
Conditions of Supply. (a) The User does not (and must not represent to any other person that the User or any other person can) acquire any right or title to, or interest in, the Distribution System or any part of the Distribution System under this Agreement.
Conditions of Supply. 4.1 Deliveries of the Contracted Product shall be at *** as indicated in the relevant Order (***, all costs included).
Conditions of Supply. 8.1 All sales made by Quotient or Suisse SA to OCD shall, except where otherwise agreed in writing, be subject to the terms herein. Any inconsistency between the terms of this Agreement and any other applicable conditions of sale shall be governed by the terms of this Agreement.
