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Exam Number : E20-393
Exam Name : Unity Solutions Specialist test for Implementation Engineers
Vendor Name : EMC
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E20-393 test Format | E20-393 Course Contents | E20-393 Course Outline | E20-393 test Syllabus | E20-393 test Objectives


Exam Title : Dell EMC Certified Specialist - Implementation Engineer - Unity Solutions (DECS-IE)
Exam ID : E20-393
Exam Duration : 90 mins
Questions in test : 60
Passing Score : 63%
Exam Center : Pearson VUE
Real Questions : Dell EMC Unity Solutions Specialist Real Questions
VCE Practice Test : Dell EMC E20-393 Certification VCE Practice Test

Dell EMC Unity Platform Concepts- Features- and Architecture 10%
- Describe the Dell EMC Unity platform architecture- features- and functions
- Describe the Dell EMC UnityVSA software defined storage solution
- Identify the Dell EMC Unity XT hardware components: DPE- SPE- DAE- expansion modules

Dell EMC Unity XT and UnityVSA Installation and Service 13%
- Describe how to install and initialize a Dell EMC Unity XT storage system
- Describe how to deploy and initialize a Dell EMC UnityVSA system
- Identify key service tasks and related resources
- Describe the Dell EMC Unity Platform service functions- including alert levels- event logs- CRU replacement

Dell EMC Unity XT and UnityVSA System Administration 7%
- Identify and describe the user interfaces for monitoring and managing the Dell EMC Unity family of storage systems
- Describe how the support and basic system settings are configured for system administration

Dell EMC Unity XT and UnityVSA Storage Provisioning and Access 25%
- Describe the different types of storage pools - traditional and dynamic - and how they are provisioned
- Describe dynamic pool expansion- considerations for mixing drive sizes and the rebuild process
- Describe how to provision block- file and VMware datastore storage
- Describe how to configure host access to block storage resources
- Describe how to configure NAS client access to SMB and NFS file storage resources
- Describe how to configure VMware ESXi hosts to access VMware datastore storage resources

Storage Efficiency- Scalability- and Performance Features 23%
- Describe the nature and use of FAST Cache performance feature
- Describe the nature and use of the Host I/O performance feature
- Describe the nature and use of the File Level Retention feature
- Describe the nature and use of UFS64 file system scalability feature and the File System Quotas feature
- Describe the nature and use of the Data Reduction efficiency feature
- Describe the nature and use of the FAST VP Tiering efficiency feature
- Describe the nature and use of Thin Clones feature
Data Protection and Mobility 22%
- Describe the nature and use of the mobility features Local LUN Move and Local NAS Server mobility
- Describe the Snapshots data protection feature and how snapshots are created
- Describe how snapshot operations are performed on storage resources
- Describe the Replication data protection feature
- Describe how to create synchronous and asynchronous replication sessions for storage resources
- Describe synchronous and asynchronous replication operations for storage resources



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EMC Implementation Practice Test

Human elements Roundtable half II: requirements development and Implementation concerns | E20-393 test dumps and Questions and Answers

clinical device & Diagnostic industry MagazineMDDI Article Index

firstly posted February 2001

a bit greater than 12 months ago, american citizens have been greatly surprised to study that clinical mistakes in U.S. hospitals have been liable for extra deaths annually than were motorway accidents, breast cancer, or AIDS. The massive number of ongoing references in the everyday press to the Institute of medication's now one-year-ancient file on clinical mistakes is a clear indication of the influence of the study on the consciousness of the universal public. The proven fact that the analyze's findings attributed a substantial percentage of error to product-design problems has additionally caught the attention of the gadget business.

more and more, groups are realizing the significance of developing and following a coherent human elements application with the identical diligence they might commit to instituting a web approach or getting ready for ISO certification. even though it can be complicated to establish clear developments in the design world, there's definite flow towards an previous and more-intensive consideration of human elements concerns within the product development technique. As reflected in the dialogue that follows, the impending liberate of the AAMI human elements regular makes it much more pressing for enterprises to have a attainable human elements program at present underway—if an organization's now not up to speed now, they may be already late.

This function represents the 2d part of MD&DI's special human components roundtable. half I, entitled "The Regulatory vital," seemed in the January 2001 difficulty.

MD&DI: in the enviornment of specifications development, may a person supply us a brief history lesson on the AAMI human factors committee requirements building efforts, and tell us when they could are expecting to see these necessities published with the aid of AAMI?

Weinger: For more than two decades, there was a very shut relationship between specifications-making actions—each national and international—and regulatory activities by using FDA. The AAMI human factors guidelines were first approved in 1988, however there become a period of about five years of undertaking in advance of that approval. The guidelines have been revised over the five-12 months length after 1988 by using a committee that covered a number of participants of the existing panel. The leading alterations reflected within the current version—which is specific HE48 1993 and is an AAMI/ANSI average—are the inclusion of human-computing device interaction suggestions in regards to designing microprocessor-controlled instruments, and the inclusion of a quick description of the human elements engineering system. starting in 1996, the committee all started taking into account on a way to revise the 1993 doc, which turned into nevertheless insufficiently particular to clinical industry wants and had some gaps because of evolving know-how.

despite the fact, a larger situation of the put up-1996 committee was that the conventional information about how one should design a screen, as an instance, changed into perhaps much less important than a broader strategy that could outline an premiere human elements design process—especially given that this manner may differ from device to gadget. So the committee started work on a separate doc that changed into meant to be a national regular for the human elements design process. That doc is at the moment out for ultimate balloting, and is expected to be authorized by using July 1, 2001. Over the closing year and a half, the committee has similtaneously begun a parallel effort to revise and extend the classical "how-to" human components design instructions that are in HE48. Their existing plan is to try this as an internet site, and in reality they very a good deal need manufacturer aid and encouragement to be capable of bring on this probability to give respectable user interface design information.

I should have outlined earlier that the AAMI human factors committee comprises, in nearly equal numbers, representatives from business, clinicians, and others with pastime or expertise in human components and clinical device design, including FDA representatives and human factors consultants.

Wiklund: could you make clear some of the feedback you made, which became that the final version of the ordinary changed into nonetheless regarded lower than top-rated when it comes to how well it is desirable to medical gadgets? in all probability you might retrace the background of why, even after a 2nd revision, it still could no longer speak to clinical devices as readily as we'd adore it to.

Weinger: I feel the huge issue, frankly, is that mainly back in 1993—and even now—we simply did not have loads of clinical equipment–selected design suggestions purchasable. even though individual device businesses have lots of capabilities and adventure (besides the fact that children how tons of it became documented is hard to claim), this counsel turned into now not public. The material that changed into purchasable to the committee just before the 1993 document consisted basically of posted requirements from different domains, especially the military. And so the committee lifted heavily from military design advice necessities, and, along side some fabric from the NRC and different published design files, tried to modify them as choicest they could for the clinical business. youngsters, it become identified at the time—and definitely due to the fact—that a few of these adjustments have been more successful than others. In particular, the human-desktop interface sections have been not modified sufficiently to tackle the needs of clinical gadget producers with admire to building exact instruments, exceptionally for vital-care functions.

MD&DI: Why did the committee in the beginning focal point on design procedure concerns instead of ideas of decent design? What are the core points of AAMI's counseled manner?

Wiklund: What i will most likely do is customise the question. As a specialist, i am requested on occasion to take a glance at a medical device and render a judgment involving its usability and defense by means of virtue of the exceptional of its user interface. Now, it is a really challenging job to do. every so often there can be some low-mendacity fruit that you can select—it truly is, evident beauty shortcomings in the design, the character of the labeling, the measurement of characters in a display, things that you can comfortably establish with the aid of inspection and software of universal principles of first rate design. however, or not it's generally very complicated to make more overarching judgments about the usability of a tool just by way of looking at it. furthermore, as a clothier, you may come up with a design that you believe would flow any litmus check in terms of good design practices, however, until you validate it in the context of a usability check, you cannot be sure that you have developed a good design.

The AAMI work and FDA's assistance do stress good design tactics, as a result of we'd all probably agree that such an emphasis represents their premiere hope for producing a great person interface. As a pragmatic purpose, it be intricate to create perfection right off the bat via advantage of unbelievable design talent being dropped at a role. A greater attainable aim is to create an iterative manner of studying clients' needs and preferences, turning those into design dreams, constructing a design thought that reflects those desires as well as good design practices, then going ahead and modeling a design and having americans engage with it and seeing how things go—and then repeating the process. You could liken it to the way you wash your hair: you wet, lather, rinse, and repeat. One could say the identical aspect about cleaning a scientific device design of any kind of human factors shortcoming. The aim is to get conclusion-users concerned in the method of expressing their needs and preferences up front, after which evaluating the product by using having them put their fingers and minds on it and seeing how things go when they try to function tasks. that's probably the ultimate means of manufacturing a design that will perform neatly.

Hasler: one of the explanations they actually center of attention on design system issues is that—although that people regularly are looking to simply pick up some sort of a established "cookbook" doc and seek the accurate "recipe" they need—there is effectively too an awful lot variation within the person interface of scientific devices for an encyclopedic assistance to work. In different words, if we're focusing on a ventilator or an infusion gadget, they might come up with top notch guidelines, however when it be a count number of the total trade, an approach emphasizing respectable procedures is at the start the best solution to proceed.

MD&DI: what's the popularity of overseas efforts to advertise human components in clinical gadget design?

Carstensen: The overseas Electrotechnical commission (IEC) is within the process of updating its big doc, IEC 60601-1, which covers widespread requirements for the protection of electromedical equipment. As a part of that accomplishing, a few 12 months ago they initiated efforts to develop a brand new collateral standard that, as soon as in region, will become part of IEC 60601-1. Its quantity is IEC 60601-6; there are 5 different collateral necessities, protecting areas such as EMC trying out. the first committee draft (CD) is scheduled for distribution to countrywide committees for hearing and remark in February 2001, however the goal date for publishing the last document is not unless the fall of 2004. That feels like a long time, however the good news is that, traditionally, companies will get wind of what is going on and procure copies of the primary and 2d CDs and respond to them. they'll react in anticipation of a typical coming down the tune, and derive plenty of the decent results well before the publication date of 2004.

The overseas commonplace—in fact a global human components engineering tenet—is based on the AAMI files. but the IEC document itself likely does not occupy greater than about 10 pages, plus an informative annex that tells you how to go about doing the job. That informative annex may be the newly revised AAMI human factors design procedure commonplace. The intent is to achieve global harmonization at the outset, as antagonistic to what they always do, which is to have a global version of a common and a lot of home requisites, after which party years later and sort of argue concerning the ameliorations and try to choose anything that is fairly harmonious. This time, we're making certain it be harmonious from the starting.

additionally, ISO Technical Committee 210 on pleasant systems has expressed an interest in becoming a member of the IEC working neighborhood it really is constructing the overseas version of the AAMI average, to be able to put out a joint ISO/IEC edition of the ordinary. What that would do is enable us to expand the scope past electromedical contraptions to encompass all medical gadget.

MD&DI: Rod, as a human components professional working at a big company, what's your view of the new rules? What are the most advantageous challenges you face in responding to them? What about can charge pressures? finally, are there transformations in the manner the rules affect the way you boost items for domestic versus overseas markets?

Hasler: involving human factors considerations within the scientific gadget business, businesses can be divided into two camps. The camp I come from recognizes the magnitude of human factors at the least as long in the past because the early 1990s. at that time, they carried out a customer-focused system to outline an IV infusion gadget, and promptly found that the function most favored via the customer was ease of use. This drove us to look the significance of hu-man factors practices, and how decent human factors could advantage us. So my introduction to human components was definitely on the advertising side—a way to make more desirable-promoting items which are effortless for shoppers to use.

and that i believe it truly is probably where you are seeing the corporations that jumped into the discipline of human components early on—they were truly employing it for the convenience of use, and to power an improved product to the consumer. people that failed to appreciate that are a bit bit in the back of as far as converting.

I consider that lots of the larger agencies adopted this equal route, and usually have lengthy-standing human elements courses. Many smaller companies are nonetheless in some thing of a catch-up mode; they are making an attempt to take into account exactly what's required and the way they can enforce it. but I believe that this law has a very strong upside for the whole clinical equipment trade—it's going to really Excellerate the trade as an entire, as far as reducing design mistakes.

MD&DI: Do you observe any differences within the emphasis on human factors in items destined for the U.S. market versus the remote places market?

Hasler: What you see a good deal less of in Europe is human components used as a part of a advertising and marketing method or strategy. related to home and overseas markets, although, one of the vital complications in the machine business is that they are likely to Excellerate items which are oriented towards and designed for a selected customer in a particular country, however are then launched to other nations with no changes. Whereas although the genuine scientific software can also stay the identical, there are sometimes differences on a country-with the aid of-nation groundwork in how the clients react to the design and make use of the gadget. So the largest situation I actually have on a worldwide entrance considerations releasing a product that was designed for one market into distinctive markets.

MD&DI: How do the new suggestions affect the advertising and marketing of contraptions that were developed earlier than the human factors regulations had been adopted? What happens with products that represent slight changes to older items that may also no longer have included respectable human elements design principles?

Wiklund: i would be satisfied to answer this question from a consultant's point of view. I feel here's going to be a superb supply of anxiousness in the future for these organizations that are not getting clear indicators as to their vulnerability in terms of promoting any product that hasn't benefited from a very good human components design method. because many groups might be introducing products that signify slight diversifications of old versions, one could argue that they should habits a radical human elements contrast of the modified design—which might infer getting client comments in the context of usability assessments, and so on. Of route, a corporation that has marketed a product for a very long time—a product that turned into at first accepted by means of FDA—could ask itself even if it in reality needs to move through all of that effort after making handiest minor changes to the product.

Compounding this whole issue is the undeniable fact that, as soon as laws are in location and individuals turn into extra privy to them, a corporation that doesn't follow good human components procedures could be accused of now not making use of due diligence in pursuing state-of-the-paintings apply. In other phrases, you carry the opportunity of legal liability publicity if a company fails to comply with the brand new common. My bet is that companies that perform minor changes to existing products will at the least need to habits a usability check to ascertain that the brand new changes are in fact good changes. they may wish to make sure that they have not inadvertently delivered different forms of issues, or somehow corrupted the preexisting design in a way that could lead to user error. So at a minimum, I believe that companies taking a conservative and careful method will seemingly begin doing more usability testing than they might have earlier than these regulations had been in vicinity.

Hasler: What i am seeing in the industry displays very a good deal what Mike has simply described. It will also be reasonably perplexing finding out a way to tackle a product that you've got been producing for, say, two decades once you appreciate that a minor characteristic has to be modified. according to all previous strategies of comparison, you would have long past forward and made the exchange for any further contraptions bought. Now, however, when you birth dealing, as an example, with the user interface, you can also realize that different points of the device can also now not meet the current regular and might deserve to be changed. besides the fact that children a corporation actually wants to support its valued clientele, you are now confronted with a full-blown venture—a whole transform—of some thing that in fact is never the product line you want to circulation into the long run. in brief, it is awfully difficult to keep in mind how the rules should be utilized to older products.




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https://spaces.hightail.com/space/v47qz1ixkg/files/fi-b43864b7-df94-478a-a224-3ce8f3de7d9a/fv-f21f3c8c-3450-43d7-be11-a0ef0fe43f82/Unity-Solutions-Specialist-Exam-for-Implementation-Engineers-(E20-393).pdf#pageThumbnail-1
https://www.coursehero.com/file/70402393/Unity-Solutions-Specialist-Exam-for-Implementation-Engineers-E20-393pdf/
http://ge.tt/9WenbY83
https://ello.co/killexamz/post/7ck0h1-fb7zrehgmio9faw
http://feeds.feedburner.com/ExactlySameE20-393QuestionsAsInRealTestWtf
https://sites.google.com/view/killexams-e20-393-exam-dumps
https://www.clipsharelive.com/video/5141/e20-393-unity-solutions-specialist-exam-for-implementation-engineers-updated-cheet-sheet-by-killexams-com
https://youtu.be/_Y8AiMie_1A
https://justpaste.it/E20-393



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