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EMC E20-597 : Backup and Recovery Specialist for Storage Administrators Exam

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Test Number : E20-597
Test Name : Backup and Recovery Specialist for Storage Administrators
Vendor Name : EMC
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Exam Title : Dell EMC Certified Specialist - Systems Administrator - NetWorker (DECS-SA)
Exam ID : E20-597
Exam Duration : 90 mins
Questions in test : 60
Passing Score : 63%
Official Training : NetWorker Fundamentals (MR-1WP-NWFUN)
NetWorker Modules Overview (MR-1WPNWMODS)
NetWorker Implementation and Management (MR-1CP-NWIM)
NetWorker Implementation and Management – Online ILT (MR-1LP-NWIM)
NetWorker Implementation and Management – Video ILT (MR-1TP-NWIM-1601)
Exam Center : Pearson VUE
Real Questions : Dell EMC NetWorker Specialist Real Questions
VCE practice test : Dell EMC E20-597 Certification VCE Practice Test

Dell EMC NetWorker Overview 10%
- Describe a NetWorker solution and its advantages
- Identify and describe the NetWorker software components and their roles, data protection functions, and terminology
- Explain the use of NetWorker control data and administrative interfaces

Dell EMC NetWorker Modules Overview 15%
- Explain how NetWorker modules work with native applications to support backup and recovery
- Explain the backup and recovery process with NetWorker modules
- Explain the functionality of various NetWorker modules; for example, NMM and NMDA

Dell EMC NetWorker Installation and Configuration 30%
- Identify and describe how to configure NetWorker backups; including client, protection group, policy and directive resources, and client save set and backup command attributes
- Explain the NetWorker backup options; including synthetic full backup, block based backup, snapshot management, and VMware backup options
- Identify and describe the features of NetWorker backup devices and how they are configured and managed; including device types, media pools, client direct backups, cloning, and staging

Dell EMC NetWorker Administration and Management 30%
- Identify and describe the NetWorker security features; including NetWorker authentication (AuthC), NetWorker user groups, logs, and configuring firewalls
- Identify and describe how the NetWorker server and NetWorker Management Console are configured and managed; for example: notifications, reports, parallelism, multi-tenancy
- Identify and describe how to recover Windows hosts and configure NetWorker in cluster environments
- Identify and describe how NetWorker recoveries are performed; for example: directed, browsable, and save set
- Describe the management and backup and recovery of NetWorker databases; for example: media and resource databases and client file indexes

Dell EMC NetWorker Cloud Enablement 15%
- Describe the NetWorker features and capabilities that support backup to and in the Cloud
- Describe how to "configure" NetWorker with CloudBoost and Cloud Tier
- Describe how to "manage" NetWorker with CloudBoost and Cloud Tier
- Describe the features and capabilities provide by the NetWorker vRealize Data Protection Extension



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EMC Storage questions

concepts for Bench testing medical instruments | E20-597 test Questions and Real test Questions

at first posted MDDI April 2003

trying out

For a hit testing, choose the appropriate tests and conduct them at the right time—in an acceptable facility.

by using Robert Mosenkis

medical devices may also be Tested at a variety of degrees in their life cycle. all through their preliminary design, it is important for the design team to determine at the least some points of performance or defense to make sure that they are on the appropriate track. extra-extensive prototype checking out usually follows completion of the preliminary design phase, to exhibit that the equipment meets its design requisites. medical trials might also comply with.

trying out for regulatory approval, to fulfill the brought up or implicit requirements of one or more regulatory businesses, is carried out next; this should be performed on production gadgets or on preproduction prototypes that reflect the manufactured product. once a tool has earned approval, construction line start-up often requires further trying out to validate the creation gadget (for example, samples from each cavity of a mold) and inspection protocols. 

Later within the existence cycle, the advertising branch could request product-checking out information for use in brochures or on the business web web site. Comparative checking out is occasionally applicable; unbiased single-product trying out can also suffice. also, if design or cloth changes are ever made to the equipment that could have an effect on performance or safety, extra testing is warranted, despite the fact that a brand new regulatory submission isn't required.

finally, further testing can also comply with a suggested opposed incident, to verify what went incorrect and why. lots of the special issues associated with this certain round of trying out are beyond the scope of this text; youngsters, the advice introduced right here can also nonetheless show advantageous.

every round of trying out requires a special strategy. Failure to Boost the foremost strategy for each and every may outcome in even more checking out at a later time, or failure of the verify consequences to meet the normal purpose. for example, the usage of an existing ordinary to look at various a special device attribute or know-how can be inappropriate. 

An example of this befell when an organization was asked to evaluate the resistance of a couple of surgical masks to blood penetration. at the time, the only present standards have been for water-repellent fabrics under extended exposure or materials subjected to liquid below pressure—these had been not appropriate. To remedy the problem, the business developed a simple check methodology that concerned squirting animal blood from a syringe for a short while.

All stakeholders have to ask three fundamental questions when developing a trying out method:

• What assessments are crucial?• What contraptions may still be validated, and when?• Who may still do the testing?

a superb approach will emerge as these questions are mentioned and answered.

What assessments Are needed?

The aim of the trying out determines what assessments are vital. whether it is early within the design cycle, the usage of crude verify setups simply to determine that the gadget will function its simple feature will doubtless suffice. For an electrocardiographic (ECG) display screen, for example, attaching electrodes to a volunteer (or the design engineer) and exhibiting the output on an oscilloscope can reveal no matter if the waveform appears like a typical ECG; comparing the fee monitor against palpated pulse will display even if the price meter is functioning. Electromagnetic compatibility (EMC) testing, for example, is evidently now not warranted at this stage. Later, the design can also be confirmed in opposition t the entire requirements of a vital normal or in opposition t each of the product specifications.

The question of whether to examine towards recognized requirements or to advance a unique verify methodology is dependent upon who will evaluation the results. requisites are written to yield constant results, no remember who applies the usual, or when. here's why so many specifications require complicated, exact, and infrequently costly look at various setups, as is the case with a these days developed commonplace for the blood-resistance trying out of surgical masks outlined prior. while careful trying out to necessities is “overkill” within the preliminary design testing, it's commonly the choicest approach in a while.

In some situations, the superior method is to adjust a typical. for example, an ISO standard includes tests for leaks in luer fittings under force or vacuum. The becoming is attached to a delegated stainless-steel becoming, and force or vacuum is utilized. but some safeguard syringes may also be used most effective with their manufacturers' proprietary needles and don't consist of luer fittings. since the theory of a leak-free connection would follow to these devices as well, it is applicable to alter the average by using substituting the proprietary needle and its fitting for the common steel fitting and applying the drive and vacuum unique in the general.

if your equipment uses a brand new expertise or contains a novel function, you may also have no choice however to increase a brand new verify formulation, since standards conveniently do not follow. a further illustration for which trying out to a standard may not be the top-quality method is when products are being compared for marketing functions. since the effects are intended for the customer, it may well be more suitable to simulate clinical use, instead of to use check device or fixtures that are average of those mandated by requisites. 

custom check methods may additionally seem to be crude when in comparison with the fairly advanced methodology of specifications. despite the fact the previous may additionally lack repeatability, and the recommendations of different verify personnel can affect the consequences, such shortcomings aren't an element when all trying out is done at one time and area, by the same individuals.

What gadgets may still Be tested, and When?

The testing purpose will regularly dictate which, and how many, gadgets to test, as well as when within the lifestyles cycle to do the checking out. Prototypes are often built the usage of materials and ideas reasonably different from these used in creation; they are usually handcrafted and finely tuned. probably the most assessments that are vital to construction instruments are not relevant at this stage; besides the fact that children, be aware about the trap hidden in their postponement.

Some assessments which are required for a comprehensive product involve aspects of the device that don't seem to be involved in typical use. EMC comes to mind, as do severe storage and working conditions and biocompatibility. whereas it's easy to delay these checks until the design is frozen, the can charge of adjustments dictated by way of verify disasters at that aspect may be high. In some such cases, the solution might be a further circular of trying out, with the conception that one of the a hit test results could be valid later, particularly if design changes aren't necessary.

the place the goal of checking out is regulatory approval (see sidebar), the check samples ought to replicate construction devices for the effects to be valid. The objective of this trying out is to reveal that a top quality equipment can be constantly produced. hence, these tests should be finished handiest after the design process is finished; although, as mentioned previous, it might no longer be vital to repeat some previous exams. 

The variety of samples proven could smartly be dictated by way of the ordinary or guideline used. Relevance and/or statistical value are top considerations. trying out a single trial of a posh electronic device is continually sufficient for regulatory approval; checking out 20 samples of a mass-produced device can be essential to show uniformity. When opting for samples, they should be as dissimilar as imperative (as an example, samples from each creation line or every mold cavity), but in keeping with the trying out aim.

Who should still Do the checking out?

In most cases, somebody universal with the equipment and its application may still look at various the product; this continually elements to doing so in-condo. In bigger businesses, a separate community can habits all testing; in smaller ones, it will probably fall to the design engineer, at the least for preliminary testing. Some companies do not understand that self-testing might also even be executed when the report is blanketed in a 510(k)––youngsters this is no longer necessarily the case for different regulatory agencies. If testing is executed in-apartment, it be a good idea to have the check plan reviewed via a person who is not too close to the design, lest something be inadvertently unnoticed.

It is a component of some organizations' exceptional procedures to have an out of doors laboratory operate final trying out, to be certain objectivity. but when an outdoor lab is used, it is going to be one with experience in trying out clinical contraptions that knows the purpose of the testing and the nature of the machine being established. A scientific equipment enterprise once submitted the simplest prototype of its electronic equipment to a native verify condominium for vibration and influence trying out. lamentably, that lab's potential was in checking out for aerospace functions, and the influence check that it advised demolished the pattern.

The main reason for the usage of an outdoor examine residence is that the examine requires really good equipment. Biocompatibility, tensile strength, environmental, and EMC trying out are examples for which the device and facilities are too costly for the occasional wants of most medical gadget establishments. but even more convenient test gadget—and the potential to make use of it––may not be needed regularly sufficient to justify buy.

impartial look at various homes can offer a few different merits, together with the following:

• Familiarity with necessities, together with talents of average interpretations or upcoming changes.• The objectivity to critique a corporation's test protocols.• journey with regulatory company expectations of testing.• testing event with an identical gadgets, that may help in check setup and performance.• Credibility with device clients––primarily when comparative checking out is achieved for advertising purposes.

Some groups are thinking concerning the confidentiality of proprietary guidance it truly is shared with a test condo, specifically one which has worked for its competitors. while most check labs might be chuffed to sign nondisclosure agreements, remember that a lab depends on its attractiveness of integrity to live on and a single lapse will destroy this recognition. So or not it's seemingly the lab may be self-motivated to retain its valued clientele' confidentiality. also, the very indisputable fact that a lab has confirmed the same gadget for a competitor makes it stronger able to serve you.

Conclusion

As is correct of numerous different endeavors, careful planning is among the most vital points of a scientific device testing undertaking. deciding on the appropriate assessments and conducting them at the suitable instances, in an acceptable facility, can increase the product building and advertising and marketing manner. 

Copyright ©2003 clinical gadget & Diagnostic Industrya


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