Pensée du 26 février : Le remords

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Pensée du 26 février : Le remords

Message par JPA » 26 févr. 2021, 01:01

Le remords
« Notre vie auparavant dominée par la culpabilité et le remords est grandement changée par cette Huitième Étape. »
Texte de base, p. 49

Juste pour aujourd’hui, je vais me servir de tout sentiment de remords comme tremplin pour guérir au moyen des Douze Étapes.

Joël de Montpellier
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Re: Pensée du 26 février : Le remords

Message par Joël de Montpellier » 26 févr. 2021, 06:50


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Re: Pensée du 26 février : Le remords

Message par lucky » 26 févr. 2021, 06:51


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Best Anti Snoring Devices Details

Message par FrankJScott » 12 oct. 2021, 15:16

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ISO Standardization Is An Essential Step In Your Business's Development

Message par FrankJScott » 13 oct. 2021, 17:20

Standards Are The Most Important Factor In Your Successful Performance On The Market
In the end, we would like to state that we've mentioned some of the most popular standards used in the medical industry. Medical practice is among today's most desired areas of human existence. Due to the growing demands for medical services, compliance with appropriate international standards is vital. We strongly encourage you to stay informed of all changes and updates to international standards. Not only can standards be utilized by the manufacturers of medical parts and equipment and equipment, but they also play important roles in domestic and environmental matters. If you have any questions about the details and specifics of the recommended documents, contact iTeh ( ) to clarify all the details you are interested in. We're always available to assist you in selecting international standards in the field where your business operates. iTeh Inc represents safe and effective advancements. Check out the top rated cen catalog standards en-1514-1-1997 blog.

Innovative Technologies As A Topic For International Standardizations
Innovative technologies are gaining control of the world. Every day each minute, every second, a brand new gadget is created, a new technique of utilizing existing technology, and the world is inevitably shifting in the wake of this. Human life is greatly affected by the availability of both digital and electrical devices, and also the growing amount of artificial intelligence. It can be dangerous to keep these devices in a state of chaos. The Internet's rapid speed of data transmission has led to an increase in the risk of leakage of information. This is why security is becoming more important every day. Today we will provide information on the technical aspects of where and how to utilize these technologies in conjunction with the international standards that are responsible for data safety. Have a look at the recommended cen catalog tc cen-tc-67-wg-3 site.

Characterization Of Bulk Material - Determination Of A Size-Weighted Fine Fraction, Crystalline Silica And Crystalline Silicon Content - Part I General Information And The Choice Of Testing Methods EN 17289-1:2020
The vast array of materials used in production complicates regulation both locally, and internationally. International standards have been developed to ease companies and organisations' entry into new markets. One of these standards is EN 17289-1: 2020.This document specifies the specifications and test methods to determine the size of the size-weighted fine portion (SWFF) and the size-weighted fine portion of crystalline silica (SWFFCS) in bulk materials.This document also provides guidance on how to prepare the sample and determination of crystallized silica using X-ray Powder Diffractometry (XRD) and Fourier Transform Infrared Spectroscopy (FT-IR).EN 17178-2 provides a method to determine the size-weighted percentage of fine particles using the size distribution that is measured. It assumes that the size distribution for the crystal quartz particles is the exact same as that of other particles found in bulk materials. EN 17289-3 describes a liquid sedimentation method for determining the fine size-weighted portion of the crystalline silica. The two methods are based upon certain limitations and assumptions that are described in EN 17289-2 and EN 17289-3 as well as EN 17289-3. If the method is validated and studied, the EN 17289-3 method could be employed to calculate other constituents.This document can be used to crystalline silica containing bulk substances that have been fully investigated and validated for determination of the fine fraction that is weighted by size or crystalline silica.The existence of the technology documentation base will help you scale up production if your area of activity is directly connected to the materials described in this document. Click here to visit our website to learn more. See the most popular iec catalog standards iec-60747-18-1-2019 info.

Software Engineering And Systems. Software Product Quality Requirements Evaluations And Evaluations (Square) For Software Products. Common Industry Format (Cif), For Usability Specifications For Users (Iso 25065.2019). EN ISO 25065:2020
In order for a business to achieve an undisputed position on an international market it is vital that they have software that is of top quality. There are specific rules for these markets that must be followed in the present. These rules are contained in documents such as EN ISO 25065: 2020.This document provides a framework and consistent language to define the user's requirements. It offers a standard industry format (CIF) that specifies the requirements of users. This includes both the content as well as the format.A user requirements specification outlines the formal requirements and documentation of an item. It can be used to aid in the development as well as the evaluation and maintenance of interactive software that is usable.User requirements, as used in this document, are A. user-system interaction requirements (including requirements system outputs and their characteristics); the second. use-related Quality Requirements that specify the quality criteria that users interact with the interactive system. This could be used to establish system acceptance requirements.ISO/IEC 25030 specifies quality requirements. The document provides a particular type of quality demand which is the quality requirements related to use. The elements in specifications for user requirements are intended to be used as an element of documentation that results from the processes described in ISO 9241-210 as well as from human centred design processes similar to those found in ISO 9241-220.This document is designed to be used by requirements engineers business analysts, product managers as well as product owners and people acquiring systems from third party. CIF's standard series covers information related to usability (as specified in ISO 9241-11 and ISO/IEC TR25060).Beyond the user-friendly aspect, requirements for usability could also be viewed from other angles including human-centric quality introduced in ISO 9241-220, and other quality aspects that are described in ISO/IEC 25210, ISO/IEC TS 2511 and ISO/IEC 25030.Although this document was designed to be used in interactivity, it can be applied to other domains. This document does no prescribe any method, process or lifecycle. The elements of the User Requirements Specification could be utilized for iterative Development which is the development of and the evolution (e.g. as in agile development).
Use of this international standard can greatly help your professional work. It can also help you structure your current system and offer new opportunities to conquer new markets and expand your business. Check out the best iso catalog standards iec-tr-80001-2-2-2012 blog.

Health Informatics Interoperability Of Devices. Part. 0701; Point-Of-Care Medical Device Communications. Service-Oriented Medical Instrument Exchange Architecture. Protocol Binding (Iso/Ieee 11073–20701 2020). EN ISO 11073-20701:2020
The use of communication technologies is in many areas and not only ones that directly relate to this field but also in medical industries. The introduction of various medical devices requires complex transformation. To facilitate these processes, international documents have been created.
This standard addresses a service-oriented medical device design and communication protocol specification. It is applicable to distributed system of PoC (Point-of-Care) medical devices as well as to medical IT systems which require data exchange and safe control over PoC medical devices. It specifies the functional components, communication relationships, and the binding to protocol specifications.The document is specific and has a limited scope. Therefore, we recommend that this document be reviewed for more information. If you have any questions you should consult managers who are specialists on international document choice. See the top rated cen catalog standards en-1789-2007a2-2014 site.