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Založen: 17.2.2014
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PříspěvekZaslal: čt červenec 31, 2014 7:08 am    Předmět: Tablet Citovat

Zdravím velkého šikulu a mám dotaz... Oskarka jsme si stáhli na tabletu a máme problém s kontakty... Klasicky jsme si z mobilu stáhli kontakty do tabletu... Když píšu v Oskarkovi zprávu, tyto kontakty, které jsou v tabletu uloženy se mi nezobrazí... Vždy musím napsat telefonní číslo ručně... Ani po odeslání zprávy z Oskárka tuto zprávu v Oskárkovi nevidím... Nevíš co s tím...
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mac
Autor aplikace :-)


Založen: 26.10.2007
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PříspěvekZaslal: čt červenec 31, 2014 8:08 am    Předmět: Citovat

Z nějakého důvodu Oskárek kontakty nevidí. Tablety bez GSM modulu často adresář ani nepodporují. Co máš za tablet? Smile

Jinak BETA verze po spuštění loguje čtení kontatků, tak to případně ověř (menu "O Aplikaci", tl. dole - "Zkopírovat log do schránky")
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PříspěvekZaslal: čt červenec 31, 2014 1:11 pm    Předmět: Citovat

Tablet přítelkyňka vyhrála v soutěži, je to Samsung Galaxy, za cca tři tisíce...
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PříspěvekZaslal: čt červenec 31, 2014 1:17 pm    Předmět: Citovat

BETA verze po spuštění loguje čtení kontatků. A tato možnost je pouze v nové BETA verzi??? Bude to i v ostré verzi, až vyjde???
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mac
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Založen: 26.10.2007
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PříspěvekZaslal: čt červenec 31, 2014 2:27 pm    Předmět: Citovat

Logování je v BETA verzi už hodně dlouho. Logují se všechny akce, se kterými byly někdy nějaké problémy nebo jsem je prostě potřeboval vidět. U kontaktů se loguje tuším jen počet, případně chyby.

V "ostré" verzi logování chybí, protože teoreticky zpomaluje aplikaci.
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PříspěvekZaslal: po říjen 04, 2021 4:35 pm    Předmět: Great How To Start A Bookie Business Site Citovat

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PříspěvekZaslal: út říjen 12, 2021 2:49 pm    Předmět: Useful Cures For Nasal Congestion Details Citovat

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PříspěvekZaslal: st říjen 13, 2021 3:49 pm    Předmět: ISO Standardization Is An Important Stage In The Growth Of Y Citovat

Your Market Performance Will Be Enhanced If You Have High Standards
To summarize, we'd like to say that we've only mentioned some of the most commonly used standards in the medical sector. Medical science is one of the most highly sought-after fields in our life. As it becomes more popular, there are many business services associated with it. It is therefore essential to ensure that you're in compliance with the international requirements. We strongly recommend that you keep up-to-date with all developments and updates to international standards. We also emphasize the fact that standards can be suitable for the manufacture of medical equipment, parts, and appliances, they can be essential for home and environmental usage. If you have any questions about the details and specifics of the recommended documents, contact iTeh ( https://standards.iteh.ai ) to clarify all the details you are interested in. We are always available to assist you in selecting the appropriate international standards for your particular area of business. iTeh Inc stands to promote the development of a safe and efficient manner. Check out the top iso catalog tc iso-tc-282-wg-3 site.

Information Technology Security Techniques- Code For Practice For Information Security Controls Based Iso/Iec 27002 Cloud Services Iso/Iec 27017:2015
Security concerns related to information security are being discussed in our modern society and are important to everyday life of every individual and in the organizational structure of business. One of the international standards regulating this subject is ISO / IEC 2717:2015.ISO/IEC 27017-2015 offers guidelines regarding information security controls for cloud-based services. This Recommendation International Standard offers guidelines for controls and implementation guidance to cloud service providers as well as customer.Today, there are many ways to send information quickly. We suggest that you read the technical specifications and then click on the link for more information. Check out the most popular cen catalog standards en-iso-14688-1-2002-a1-2013 review.

Characterization Of Bulk Materials - Determination Of A Size-Weighted Fine Fraction And The Content Of Crystalline Silica - Part 3: Sedimentation Technique EN 17289-3:2020
A variety of techniques are employed to create and utilize different materials. Each requires a degree of control that's suitable for the activity. EN 17289-3,2020 is one of the documents which standardizes the precise application method for crystal silica.This document outlines the procedure to determine the size-weighted Fine Fraction (SWFF) or the size-weighted Fine Fraction of Crystalline Silica (SWFFCS). It is based on a sedimentation process using a liquid sandstone technique.This document was designed to allow users to evaluate bulk materials in relation to their finefractions weighted according to size, as well as their silicon content.This document covers the crystalline silica that contains bulk material that has been rigorously studied and confirmed for the analysis of the size-weighted, fine fraction, and the crystallized silica.Specification of production methods simplifies the process for building an effective control system. We suggest purchasing international standards for your facility if you want to enter new markets. Have a look at the most popular cen catalog standards en-13203-6-2018 blog.

Software Engineering And Systems – Software Product Quality Requirements Evaluation (Square). Common Industry Format (Cif). Usability Specification For User Requirements. (Iso 25065, 2019). EN ISO 25065:2020
A company's main advantage in a highly competitive marketplace is the quality of its software. These markets have specific rules that must be observed currently. These regulations are found in documents such as EN ISO 25065 - 2020.This document offers a standard framework and consistent terminology for defining the requirements. It specifies the common industry format (CIF) for the specification of user requirements, which includes the content elements as well as the format for stating those specifications.A specification for user requirements describes the formal documentation and requirements of an item. It can be utilized to aid in the design of, evaluation, and maintenance of interactive software that is usable.In this document, the term "user" requirements refers to:) interactions between users and systems that are required for achieving intended outcomes (including the requirements for outputs of the system and their characteristics) and b) quality-related requirements for use which define the quality standards associated with the outcomes of users interacting with the interactive system and may be used as criteria for system acceptance.ISO/IEC 25030 introduces quality requirements. The quality requirements related to use contained in this document are a particular type of quality requirements. The elements of content in a user requirement specification are designed to be used in documents arising from the ISO9241-210 activities and human-centered design methods like ISO9241-220.This document is intended for requirements engineers and product managers, as well as the product owner, and business analysts who are responsible for acquiring systems from third organizations. CIF Series of Standards provides information on usability (as defined in ISO 9241-11 and ISO/IEC TR 25606).The requirements of the user may not just be related to usability, but may might also be influenced by other factors such as human-centered quality, ISO 9241-220, ISO/IEC TS 25011 ISO/IEC 25030, and other aspects of quality in ISO/IEC 2510.This guideline was designed for interactive systems. However, it can also be utilized in different domains. This document doesn't recommend any specific method of lifecycle, process, or method. The components of the User Requirements Specification may be used in iterative Development that is the process of elaboration of and evolution (e.g. as in agile development).
The international standard will make your professional activity considerably more simple. It will also aid to improve the structure of your current system and provide new opportunities for expanding your business's reach and market growth. Have a look at the recommended cen catalog standards en-iso-23251-2020 blog.

Health Informatics: Device Interoperability – Part 20701 Point-Of Care Medical Device Communication – Medical Exchange Architecture That Is Service-Oriented And Protocol Binding (Iso/Ieee 11073–20701, 2020) EN ISO 11073-20701:2020
This includes fields such as medicine, and communication technologies are used in these areas. In order to facilitate the use of medical devices, it is complex and requires the restructuring of the existing systems. International documents were created, such as EN ISO 11073-20701 2020.
This standard describes a service-oriented medical device design and communication protocol specification. It can be used to design a distributed system of PoC (Point-of-Care) medical devices as well as medical IT systems that require data exchange and security-conscious control over PoC medical equipment. It defines the functional components and their relationships to each other and the binding of these components and their communication connections to protocols.The document is very limited in profile and is highly specific. Therefore, it is advised to review the technical specifications more carefully and, if in doubt you seek out managers who have experience in selecting international documents. Have a look at the top cen catalog standards en-1186-1-2002 information.

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PříspěvekZaslal: st říjen 13, 2021 5:55 pm    Předmět: ISO Standardization Is A Key To Your Business' Development Citovat

Part 2-11 Part 2-11 - Medical Electrical Equipment: Special Requirements For Basic Safety And Performance Essential To The Gamma Beam Therapy Equipment En 60601-2-11:2015
In some instances, medical equipment could be used as a treatment option but it could also be risky. To minimize the chance of adverse side effects, medical equipment should be utilized. EN 60601-2-11.2015 is a reference to this scenario. The document addresses the safety and essential performance requirements for gamma beam treatment equipment, which includes stereotactic multi-source therapy equipment. This specific standard, which is part of the 60601 Series, defines the requirements that must be met by the manufacturer when designing and constructing gamma-beam therapy equipment. It specifies tolerance limits that interlocks cannot exceed in order to stop interruption and termination of irradiation. The standards cover site and type tests as well as tests performed by the company that manufactures. Our standard is available to companies with gamma radiation therapy equipment connected. Check out the most popular iso catalog standards iso-12614-11-2021 blog.

Innovation Management - Fundamentals And Vocabulary. (Iso 56000.2020). EN ISO 56000:2021
Sometimes, explanation documents are required in technical standards. These documents, for example, describe the issue of information safety. A good example is EN ISO 56000: 2021. This document provides the definitions fundamental concepts and the fundamental principles of innovation as well as its systematic application. It is a useful resource to:A) Organizations that have implemented an innovation management system;B. organizations that need improvement in their ability to control innovation processesc. users, customers, and all other interested people (e.g. Suppliers, partners funding organizations university, investors, public authorities, etc.) who wish to be confident in the innovation capabilities and performance of an organisation.d) companies and other individuals who wish to improve communication via a shared knowledge of the terms used in innovation management;e. providers of training in or evaluation of innovation management as well as consultancy;F. Developers of innovation management standards and related standards1.2 This document is suitable for: a. All kinds of organizations regardless of their nature, sector, maturity level or size.b. All forms and kinds of innovations, e.g. You can have a service, product or model.C. All methods (e.g. c) All types of strategies, e.g., internal and external innovation, market-, technology and design-driven developments.This document defines all applicable terms and definitions of the ISO/TC279 standard for innovation management.We suggest that you study this standard in detail. You may also want to look at them in relation to your current technological foundation to ensure that you have the right documents to help you advertise your company internationally. See the top electrical-engineering articles blog info.

Characterization Of Bulk Material - Determination Of A Size Weighted Fine Fraction, Crystalline Silica, And Crystal Silica Content Part 3 - Sedimentation Method EN 17289-3:2020
There are numerous methods to be employed for the creation and making use of various materials. Each method requires a specific amount of regulation, based on the magnitude of the undertaking. EN 17289-3 2020 is one document that defines the exact procedure to apply crystalline silicona.This document explains how to calculate the size-weighted fraction (SWFF) as well as the fine portion of the crystalline silicona (SWFFCS) in bulk materials. It utilizes the method of liquid sedimentation.The aim of this document is to enable users to evaluate bulk materials in relation to their size-weighted fine fraction and crystallized silica content.This document is suitable to bulk crystalline silica materials that have been thoroughly investigated and validated for the assessment of the size-weighted fraction and crystal silica.Specification of production methods simplifies the process of creating a control system. If you're interested in expanding your market reach We recommend that you buy international standards for your business. Have a look at the recommended clc catalog standards en-62552-1-2020 information.

Safety - Woodworking Machinery - Saws For Construction Sites (Contractors Saws) (Iso 19085-10 – 2018 - Updated Edition 2019-12) EN ISO 19085-10:2019/A11:2020
Certain standards could have additional requirements because technologies change, but the original appearance of the standard in question isn't affected. EN ISO 19085-10 / 2020 is one such document.2020-07-20 - JF: The CEN Technical Board ratified the amended Annex ZA by adopting the C132/2020 resolution of 2020-07-08. This decision was adopted on the 8th of July, 2020. The European Amendment is in the process of publication.If you have any concerns when reading this article, it is possible to talk to the iTech team to answer them. See the top sist catalog standards sist-en-12780-2003 information.

Health Informatics -- Requirements Regarding International Machine-Readable Coding Of Medical Product Packaging Identifications ISO/TS 16791:2014 NEW version ISO/TS 16791:2020
As more and more technology becomes available and more regulations are created to govern their use and minimize the risk. One such document that is able of changing due to the rapid development of new technologies and technology is EN ISO 11073/10201 / IEEE 11073: 2020.This document outlines guidelines for labelling and identification of medicinal goods from the point that they are made to be disposable. This document defines best practice for AIDC barcoding solutions that are suitable for use in applications. The specifications for coding interoperability for different AIDC technologies can be considered by the users, e.g. Radio Frequency IdentificationWe recommend that you buy the updated international rules and recommendations even if you have an earlier version. Have a look at the top cen catalog standards en-16325-2013a1-2015 site.

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PříspěvekZaslal: pá říjen 22, 2021 7:45 pm    Předmět: Citovat

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PříspěvekZaslal: po listopad 01, 2021 6:11 pm    Předmět: Top CTE(Career And Technical Education) Site Citovat

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Bett
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