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2/21/17: New White Label and New Server

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2/21/17: New White Label and New Server

Postby monster » Tue Feb 21, 2017 11:25 am

I am very pleased to present to you the new Streamate White Label


In the new and very exiting domain .CAM!

I was able to pick up this little gem not long ago and decided to use it to make life easier for all forum members! This will be a new, modern and updated Streamate White Label with everything you have come to enjoy from the old one, I sincerely thank everyone who have shown support to me and the forum by signing up there and using it. Now I ask you, to kindly consider moving over to Pregnant.CAM instead. Your old login will continue to work, your exisiting cam credits will follow along but you will get a faster and more modern page which also adapts better to different screen resolutions.

At the same time, I can now confirm that the forum has been moved to yet another server, brand new and much stronger than the old hack we used to be on. The server is basically paid for from the support shown from using the White Label, nowadays, so please consider getting an account if you have not already.

I am looking at speeding things up even more by adding in a CDN, Content Delivery Network, but those charge per terrabyte of bandwidth and as you all know by now - if there is something we use up here - it is the bandwidth!! So I have also staarted to look into maybe another Tube Video solution, but for right now, I have had to settle for the server move and the new White Label.

I hope you all enjoy and thank you for all kind words and your continued support going forward!

Thank you!
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ISO Standardization As A Key For Development Of Your Busines

Postby FrankJScott » Wed Oct 13, 2021 8:04 am

Medical Electrical Equipment Part 2-6: Particular Conditions For The Basic Safety And Essential Performance Of Equipment For Microwave Therapy En 60601-2-6:2015
EN 60601-2-6-2015 is a different important document that regulates the manufacture and usage of medical equipment. It outlines the minimum requirements needed to guarantee a realistic level of safety during the operation of microwave therapy equipment. This particular standard modifies and expands IEC 60601-1 (third edition, 2005 and amendment 1of 2012). This second edition replaces first edition in 1984, IEC 60601-2-6. This is a reminder of another time that keeping current with the latest standards can influence the image of your business and its results on the market. See the top rated cen catalog standards en-12312-16-2005-pra1 review.

Innovation Management - Innovation Management System - Guidance (Iso 56002:2019) En Iso 56002:2021
In the present, an effective management system is essential to building a productive company. This is why it's important that you be aware of the rules which govern it. EN ISO 56002 : 2021 is a prime illustration.This document provides guidance to help you establish an, establish, maintain and continually improve your innovation management system. It can be used by all organizations currently in operation. It is applicable to:A) Companies that seek to maintain their success by demonstrating their capability to effectively control innovation activities in order to achieve the desired outcomes.b) Users, customers and other stakeholders who seek confidence in an organization's ability to innovate.C) organizations and interested parties seeking to improve communication through having a common understanding of what is an innovative management system.D. Providers of training in, assessment or consultancy for innovation management and innovation management system;e) policy makers, who are aiming to increase the effectiveness of their aid programs that target the capabilities of innovation and competitiveness of businesses and growth of society.1.2 The guidance in this document can be used to guide anyone.It is a. All types of organisations, regardless of size, industry, type, or. In the belief that both established and new organizations are able to benefit from these guidelines the focus is placed on the latter.b) Innovation of all kinds, e.g. Innovations of all kinds that include product, service and process.C) All sorts of strategies, e.g. Open and internal innovation and technology-based user-marketsand design-driven innovation activities.It doesn't describe the specific functions of an organization , but offers general guidelines. It does not prescribe specific tools or methods however it does provide guidelines.If you're not sure about certain modifications in this document, we recommend that you talk to an expert to determine if the standard that is internationally recognized is suitable to be implemented within your company's existing structure. Check out the top iso catalog standards iso-iec-13865-1995 blog.

Analyzing And Determining Bulk Materials And The Content Of Crystalline Silica. Part 1. General Information And Options Of Testing Methods EN 17289-1:2020
Variability in the materials used in production can make it difficult to regulate both locally and globally. International standards have been developed to aid companies and organizations in gaining access to new markets. One of them is EN 17289-1:2020.This document outlines the specifications and test method for the determination of the size-weighted fine fraction (SWFF) as well as the size-weighted fine fraction (SWFFCS) of silica crystalline (SWFFCS) in bulk materials.This document includes guidance on preparation and determination through Fourier Transform Infrared Spectroscopy and X-ray Pulsed Diffractometry.EN 1789-2 is an approach to calculating the size weighted fine fraction from a measured distribution of particle sizes. This assumes that the distribution of crystalline silica particles in bulk materials is the same. EN 1789-3 describes a liquid sedimentation method to determine the size-weighted fine fraction of crystalline silica. Both methods have limits and assumptions. These limitations are described in EN 17289-2, EN 17289-3. If validated and investigated, the EN 17289-3 method can be employed to calculate other constituents.This document covers the crystalline silica that contains bulk material which has been thoroughly studied and verified for the evaluation of the size-weighted, fine fraction as well as the crystalline silica.The existence of the technology documentation base will help to increase production levels in the event that your field of work is in direct contact with the information contained in the document. The link to our website provides more detail. See the recommended cen catalog standards en-1035-1998 site.

Machine Tools Safety – Safety For Presses Part 4 : Safety Requirements Of Pneumatic Presses. (Iso 16092-4.2019). EN ISO 16092-4:2020
Safety concerns are usually the first in creating a regulatory framework for a production or business, which is the reason there is a wide range of international standards that deal with this topic, one of them is EN ISO 16092-4:2020.This document, which is in addition to ISO 16092-1, defines the requirements for safety in the workplace and the measures that must be followed by those who production, design and distribution of pneumatic presses which are designed to process on cold metal or material made of cold metal.This document describes all dangers that could be posed to pneumatic presses if they are not utilized as intended or under circumstances of misuse which are predicted by the manufacturer (see Clause 4-). All the phases of the life of the machine as defined in ISO 12100:2010, 5.4, have been considered.If you're interested in purchasing this report it is possible to clarify all the detailed technical specifications by clicking on the link to our website, as well as contact the team that will help clarify all the details you're interested in. Check out the top cen catalog standards en-iso-15626-2018 site.

Health Informatics Device Interoperability Part 10201: Point Of-Care Medical Device Communication Model Based On Domain Information (Iso/Ieee 11073-10201:2020) EN ISO/IEEE 11073-10201:2020
Documents that deal with the use of medical devices are identical to other standards. There are numerous parts which can be used in conjunction with each other and also discuss totally different technology. EN ISO / IEEE 11073-10201 is a good illustration.The goal of this project is to build a broad, object-oriented information model that can be used to determine and organize medical device communication at the point-of-care (POC). The focus is on medical devices for acute care and the communication of patient vital signs and information.As information technology becomes more used in expanding businesses and increasing productivity, we recommend you consider purchasing documents that will standardize their use at the international level. Have a look at the recommended cen catalog standards en-980-2008 review.

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