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EMC E20-555 : silon Solutions and Design Specialist for Technology Architects Exam

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Test Number : E20-555
Test Name : silon Solutions and Design Specialist for Technology Architects
Vendor Name : EMC
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E20-555 test Format | E20-555 Course Contents | E20-555 Course Outline | E20-555 test Syllabus | E20-555 test Objectives


Exam Title : Dell EMC Certified Specialist - Technology Architect - Isilon Solutions (DECS-TA)
Exam ID : E20-555
Exam Duration : 120 mins
Questions in test : 60
Passing Score : 60%
Exam Center : Pearson VUE
Real Questions : Dell EMC Isilon Solutions and Design Specialist Real Questions
VCE practice questions : Dell EMC E20-555 Certification VCE Practice Test

Isilon Infrastructure 20%
- Describe the nature and use of Isilon nodes, components, node pools, and node compatibilities
- Describe the nature and use of latency, sequential versus random access, and endurant cache
- Describe the nature of Isilon networking, Access Zones, and use of SmartConnect

Isilon Management, Identity Management, and Advanced Applications 47%
- Describe how to determine when to use SnapshotIQ when snapshots are not recommended
- Describe data requirements regarding SmartPools, File Pools, and CloudPools
- Describe data requirements regarding SyncIQ, SmartQuotas, SmartDedupe, Antivirus, and SmartLock
- Describe the client access, client permissions and client protocol access on the Isilon cluster
- Describe the nature and use of job engines
- Describe the nature and use of RBAC and ZRBAC
- Describe journaling, file striping, data protection, metadata, and caching
- Describe replication and recovery

Solution Design Process 7%
- Describe the information requirements for designing an Isilon solution, including determining hardware and software capacity, file server consolidation, file size considerations, performance sizing impact, data types, and I/O characteristics

Sizing Considerations 18%
- Describe how data availability and protection are implemented and measured on an Isilon cluster.
- Describe how disk space is utilized for small and large files and its effects on protection overhead.
- Describe how I/O patterns and latency requirements impact workflows on the Isilon cluster
- Describe the challenges and considerations for configuring backup and archive workflows

Workload Analysis Tools 8%
- Describe the cluster monitoring with InsightIQ and isi statistics
- Describe the nature and appropriate use of workflow analysis tools: iostat, iperf, tcpdump, Wireshark, NFSstat



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EMC test Questions

thoughts for Bench checking out clinical gadgets | E20-555 Test Prep and test dumps

at the start published MDDI April 2003

checking out

For a success trying out, choose the correct checks and habits them at the correct time—in a suitable facility.

by using Robert Mosenkis

clinical contraptions will also be established at numerous tiers of their existence cycle. all through their initial design, it's crucial for the design team to investigate at least some facets of efficiency or security to be certain that they are on the appropriate track. greater-extensive prototype trying out always follows completion of the initial design phase, to reveal that the machine meets its design requirements. medical trials may comply with.

trying out for regulatory approval, to satisfy the mentioned or implicit requirements of one or more regulatory groups, is carried out subsequent; this should still be finished on construction instruments or on preproduction prototypes that replicate the manufactured product. as soon as a device has earned approval, creation line birth-up commonly requires additional trying out to validate the production equipment (as an example, samples from every cavity of a mould) and inspection protocols. 

Later in the existence cycle, the advertising and marketing branch could request product-testing statistics for use in brochures or on the business web web site. Comparative trying out is every so often acceptable; independent single-product testing can also suffice. additionally, if design or fabric changes are ever made to the machine that might have an effect on efficiency or security, extra trying out is warranted, notwithstanding a new regulatory submission isn't required.

ultimately, additional testing may additionally observe a suggested adverse incident, to determine what went incorrect and why. most of the special concerns linked to this selected circular of testing are beyond the scope of this text; although, the information presented here may also nevertheless show positive.

each round of checking out requires a different approach. Failure to develop the top-quality method for each might result in even more trying out at a later time, or failure of the test results to fulfill the long-established purpose. for instance, the use of an present normal to examine a different machine attribute or expertise may be inappropriate. 

An example of this occurred when a company became requested to compare the resistance of a number of surgical masks to blood penetration. at the time, the handiest present specifications had been for water-repellent fabric below prolonged publicity or materials subjected to liquid under pressure—these have been now not suitable. To remedy the difficulty, the enterprise developed a simple check methodology that concerned squirting animal blood from a syringe for a short while.

All stakeholders ought to ask three fundamental questions when setting up a checking out approach:

• What tests are vital?• What devices should still be demonstrated, and when?• Who may still do the testing?

an effective method will emerge as these questions are discussed and answered.

What assessments Are vital?

The aim of the trying out determines what tests are vital. whether it is early within the design cycle, the use of crude test setups simply to check that the gadget will perform its simple function will doubtless suffice. For an electrocardiographic (ECG) monitor, for instance, attaching electrodes to a volunteer (or the design engineer) and exhibiting the output on an oscilloscope can exhibit even if the waveform looks like a customary ECG; evaluating the expense screen against palpated pulse will reveal whether the expense meter is functioning. Electromagnetic compatibility (EMC) checking out, for example, is obviously now not warranted at this stage. Later, the design can also be established in opposition t the whole requirements of a valuable average or towards each of the product standards.

The query of whether to look at various in opposition t diagnosed requisites or to Strengthen a different check methodology is dependent upon who will evaluation the results. specifications are written to yield constant consequences, no rely who applies the normal, or when. this is why so many specifications require complex, precise, and infrequently expensive examine setups, as is the case with a currently developed average for the blood-resistance trying out of surgical masks outlined previous. while careful trying out to requisites is “overkill” in the initial design trying out, it's frequently the premier approach afterward.

In some circumstances, the most excellent approach is to adjust a typical. as an instance, an ISO usual includes exams for leaks in luer fittings beneath pressure or vacuum. The becoming is attached to a chosen stainless-steel fitting, and power or vacuum is applied. but some safety syringes may also be used only with their manufacturers' proprietary needles and do not consist of luer fittings. since the concept of a leak-free connection would apply to these instruments as well, it is appropriate to alter the usual by substituting the proprietary needle and its becoming for the average metal fitting and making use of the drive and vacuum exact in the common.

in case your machine uses a new know-how or contains a novel characteristic, you may additionally have no choice but to strengthen a new examine system, due to the fact that requisites easily don't apply. a different example for which testing to a common may also now not be the optimal strategy is when items are being compared for marketing functions. because the outcomes are meant for the client, it could be better to simulate scientific use, rather than to make use of examine equipment or fixtures that are average of those mandated by way of necessities. 

customized examine methods may seem to be crude when compared with the enormously advanced methodology of standards. however the previous may additionally lack repeatability, and the recommendations of distinctive verify personnel can affect the consequences, such shortcomings aren't a factor when all trying out is carried out at one time and vicinity, by means of the identical people.

What devices should still Be tested, and When?

The checking out aim will frequently dictate which, and how many, instruments to look at various, as well as when within the life cycle to do the trying out. Prototypes are sometimes built the use of materials and strategies fairly diverse from those utilized in creation; they are constantly handcrafted and finely tuned. probably the most checks which are critical to construction devices aren't applicable at this stage; despite the fact, be aware of the lure hidden in their postponement.

Some tests that are required for a entire product involve facets of the device that don't seem to be concerned in standard use. EMC comes to mind, as do severe storage and operating conditions and biocompatibility. whereas it is handy to lengthen these exams unless the design is frozen, the cost of alterations dictated via check failures at that element may well be high. In some such cases, the solution could be an extra round of checking out, with the concept that one of the vital a hit look at various consequences might possibly be legitimate later, chiefly if design alterations aren't mandatory.

the place the goal of testing is regulatory approval (see sidebar), the examine samples need to replicate production devices for the consequences to be valid. The objective of this trying out is to show that a high quality equipment will also be continuously produced. for this reason, these tests have to be performed handiest after the design method is finished; however, as outlined previous, it may now not be quintessential to repeat some old checks. 

The variety of samples validated could well be dictated with the aid of the typical or tenet used. Relevance and/or statistical value are top concerns. testing a single sample of a fancy electronic equipment is constantly sufficient for regulatory approval; testing 20 samples of a mass-produced device can be mandatory to exhibit uniformity. When settling on samples, they may still be as varied as quintessential (as an example, samples from each and every creation line or each mildew cavity), however per the testing purpose.

Who may still Do the trying out?

In most cases, someone generic with the machine and its software should still test the product; this continually facets to doing so in-apartment. In greater corporations, a separate community can behavior all trying out; in smaller ones, it could actually fall to the design engineer, at the least for initial testing. Some groups do not understand that self-checking out may additionally also be carried out when the file is protected in a 510(ok)––youngsters this is no longer always the case for other regulatory corporations. If trying out is finished in-condominium, or not it's a good suggestion to have the look at various plan reviewed by using somebody who is not too near the design, lest anything be inadvertently ignored.

It is part of some corporations' great techniques to have an outside laboratory function last checking out, to be certain objectivity. but when an outdoor lab is used, it would be one with event in testing scientific gadgets that understands the aim of the checking out and the nature of the device being demonstrated. A clinical device firm as soon as submitted the best prototype of its electronic equipment to a local verify residence for vibration and affect testing. regrettably, that lab's competencies changed into in checking out for aerospace purposes, and the influence look at various that it advised demolished the sample.

The main reason behind using an outside check house is that the look at various requires specialized equipment. Biocompatibility, tensile strength, environmental, and EMC testing are examples for which the device and amenities are too costly for the occasional needs of most clinical equipment enterprises. but even less demanding test machine—and the talents to use it––could not be vital commonly satisfactory to justify buy.

independent look at various residences can offer a few different advantages, including right here:

• Familiarity with necessities, including knowledge of general interpretations or upcoming adjustments.• The objectivity to critique a company's examine protocols.• adventure with regulatory agency expectations of checking out.• trying out journey with equivalent gadgets, that could support in test setup and efficiency.• Credibility with device clients––certainly when comparative checking out is done for advertising applications.

Some organizations are panic about the confidentiality of proprietary suggestions it's shared with a check condominium, certainly one that has worked for its competitors. whereas most examine labs may be satisfied to sign nondisclosure agreements, remember that a lab relies on its attractiveness of integrity to live on and a single lapse will smash this recognition. So it be doubtless the lab should be self-influenced to keep its clients' confidentiality. also, the very proven fact that a lab has validated the same gadget for a competitor makes it superior in a position to serve you.

Conclusion

As is true of numerous different endeavors, careful planning is among the most essential features of a clinical gadget checking out undertaking. settling on the appropriate assessments and conducting them at the correct instances, in an acceptable facility, can enhance the product building and advertising manner. 

Copyright ©2003 clinical equipment & Diagnostic Industrya


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