Development Planning a.) If the order to the supplier includes developing duties, the requirement specification of the contracting partners has to be in written form for example as a target specification. The supplier obligates himself already in the planning phase of products, in operations and other trans-sectoral duties to apply project management and to grant examination into the project documentation to the customer by request.
b.) All the technical documents necessary for the support of the standard development like specifications, drawings, parts lists, CAD data must be checked on receipt by the supplier on completeness and consistency. If it is recognizable that the claims agreed upon in the technical documents contain faulty, unclear or incomplete descriptions of the product, these are to be indicated to the customer unsolicited in an adequate form. The same is valid, if product requirements can be substituted with more suitable, more economic and more effective procedures.
c.) For the development stage the contracting partners agree to apply suitable preventive methods of the quality planning. The experiences (process expiries, process data, ability studies etc.) from similar intentions are to be considered. Features with special demands for the documentation and archiving are to be fixed.
d.) For prototypes and pre-standard parts the production and testing terms are to be aligned and documented between customer and supplier. Aim is to produce the parts under production-oriented conditions.
e.) For the known – regulated or agreed – function-relevant features the supplier must carry out analyses of the suitability of the used production facility and document it. If agreed ability values are not achieved, the supplier must either optimize his facilities and processes accordingly or carry out adequate checks in the manufactured products to prevent defective deliveries.
f.) Before starting serial production and within serial production the supplier has to carry out the process and product release according the guidelines of VDA Band 2 (PPF) or QS 9000 (PPAP). The same approach is valid for:
1. Product changes
2. Tool changes 3. New production of tools 4. Process changes 5. Material changes
Development Planning. Prior to initiating clinical testing with the Licensed Product, BMI has provided BII a copy of the first clinical protocol for a Phase II clinical trial for the indication of treating viral hepatitis. Such protocol is attached to this Agreement as Appendix D. Both BII and BMI acknowledge that such protocol is subject to regulatory approval and to agreement with clinical investigators. Prior to initiating additional clinical trials for viral hepatitis or clinical testing for any other indication, BMI will also provide to BII a suitably detailed protocol or protocol outline for any other said clinical trial. BII will have the right but not the obligation to provide comments on each protocol or protocol outline to BMI. BMI may, at BMI’s discretion, modify any protocol in response to the comments or suggestions made by BII.
Development Planning. (1) The Contracting Parties shall take all necessary measures, within the framework of their respective national laws, to ensure that conservation and management of natural resources are treated as an integral part of development planning at all stages and at all levels.
(2) To that effect they shall, in the formulation of all development plans, give as full consideration to ecological factors as to economic and social ones.
(3) The Contracting Parties shall, where necessary, take appropriate action with a view to conserving and managing natural resources of significant importance for two or several Contracting Parties.
Development Planning cunova shall ensure that it provides the contractual partner with the specifications with all relevant documents such as drawings, parts lists and CAD data at an early stage and in full. The contracting party checks the specifications, including all technical documents, for completeness and consistency. cunova must be informed of any defects detected in the process. These are to be eliminated by mutual agreement. The Contractor undertakes to apply project management as early as the planning phase of products, processes and other cross-departmental tasks and to provide cunova with insight into the project schedule upon request. In the development phase, the parties must apply appropriate preventive methods of quality planning such as manufacturability analysis, fault tree analysis, reliability calculation, FMEA, etc. The experience (process flows, process data, capability studies, etc.) from similar projects must be taken into account. Characteristics with special requirements for documentation and archiving must be defined. For prototypes and pre-series parts, the manufacturing and testing conditions must be agreed and documented between cunova and the contractual partner. The aim is to manufacture the parts under near-series conditions. For the agreed product and process characteristics, the contractual partner must carry out and document analyses of the suitability of the production equipment used. If specified capability parameters are not achieved, the contractor must either optimize its equipment accordingly or carry out suitable tests of the manufactured products in order to rule out defective deliveries. Prior to the start of series production, the process and product release procedure must be carried out in accordance with cunova's process and procedure instructions. Design or development approvals by cunova must be given prior to the production process and product release procedure.
Development Planning. 1 HMPPS Management Information System (MIS) The MIS Database requires updating to ensure accurate and efficient recording and reporting of KPIs and MI. HMPPS and the Prisons will develop the MIS which sits on the Virtual Campus system to record and report all learning and skills activity in the Public Sector Prisons. For Prisons – ‘Starts’ means Starts (Minus Agreed Leavers) Starts Completed formula Performance Completion Rate 100 80 80 / 100 80% of those starting a Percentage of Learners x 100 = course Completed a who Start a course course. against the number who Completed a course. No. Achieved Completed Formula Performance Attainment 60 80 60 / 80 80% of those who Percentage of Learners X 100 = Completed a course who Achieved a and Achieved a Qualification against the Qualification number who Completed a course. Starts No. achieved Formula Performance Success 100 66 65 / 100 70% of those who start Percentage of Learners X 100 = a course Achieved a who Achieved a Qualification Qualification against the number who Start
Development Planning. Incorporate the physical manifestations of Pillar initiatives into a holistic and integrated planning and development process, and create strategies around project phasing, occupancy, statutory and regulatory matters, and implementation.
Development Planning. Prepare Preliminary CAM Program & Budget
Development Planning. Special Adviser.—Amina Mohammed (Nigeria).
Development Planning. Staff support the Heritage Designation (HD) and the Heritage Revitalization Agreement (HRA) for the subject property. The applicant has applied to have the existing heritage building, known as the Xxxxxxxxx House designated with an HD Bylaw. This will ensure long-term protection of the heritage asset through municipal bylaw, a power afforded to municipalities by the Local Government Act. Once the property is designated by bylaw, the owner must obtain a Heritage Alteration Permit to make any exterior alterations in the future. This is an acknowledgment that some changes to the protected heritage property will be inevitable over time as heritage buildings must be useful and safe like any other. The Official Community Plan (OCP) encourages the formal protection of heritage buildings and the consideration of adaptive reuse as a strategy to facilitate it. In exchange for restoring and protecting the heritage building, the property owner is proposing an HRA, which is a formal, written agreement with the City regarding the subject property’s land use regulations. An HRA is a powerful and flexible tool under the Local Government Act to suit unique properties and situations. The terms of the agreement will supersede the Zoning Bylaw and propose specific use, density and siting regulations (e.g. landscaping and parking) for mutual benefit between the property owner and City. The land use and development regulations for the HRA were developed by Staff in collaboration with the applicant. The proposed rehabilitation and adaptive reuse of the heritage building to an office commercial space will be carried out consistent with national heritage standards outlined in the Standards and Guidelines for the Conservation of Historic Places in Canada with the process monitored by a third-party Registered Heritage Consultant. Given the application timing, the City’s Heritage Advisory Committee (HAC) was not in operations, and so in lieu of that typical review, the applicant was required to retain the services of a Registered Heritage Consultant to review and comment on the proposed design (Attachment B). The Heritage Consultant identified that the proposal meets several key Heritage Conservation Area Guidelines and is generally in keeping with the Standards and Guidelines for the Conservation of Historic Places in Canada. Additionally, the proposal is consistent with the City of Kelowna’s Adaptive Reuse Guidelines for Residential Heritage Buildings, with its residential componen...
Development Planning. If the order to the supplier includes engineering work, the requirements are to be defined in writing by the contract partners, e.g. in the form of a requirements specification. The supplier undertakes to use project management in the planning phase of products, processes and other tasks across all departments and to allow BING to view the project plan upon request. All technical documents necessary to support development of the series such as specifications, drawings, parts lists and CAD data, have to be checked by the supplier after receipt for completeness and overall freedom from contradiction with regard to their foreseen application purpose; BING must be informed of any deficiencies identified. During the development phase, the contract partners must apply suitable preventive quality planning methods such as e.g. producibility analysis, fault tree analysis, reliability calculation, FMEA etc. The experiences (processes, process data, capability assessments etc.) from similar projects are to be considered. Characteristics with special documentation and archiving requirements are to be defined. The production and test conditions for prototypes and pilot production parts are to be agreed and documented between BING and the supplier. The aim is to produce the parts under almost series conditions. The supplier has to carry out and document analyses about the suitability of the used production plants for all characteristics relevant to functions. If stipulated capability characteristics are not fulfilled, the supplier either has to optimise his plant or carry out suitable tests on the manufactured products in order to rule out faulty supplies. Prior to the start of series production, the supplier has to carry out production process and product approval according to VDA Volume 2. Should BING demand a design approval, then this has to be carried out prior to the production process and product approval. When issuing the production process and product approval, the machine capability index and/or process capability index for agreed characteristics are to be stated, if demanded by BING. Version 6 | 2022-08-03
