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ST0-093 - Symantec Data Loss Prevention 10.5 (STS) - Dump Information

Vendor : Symantec
Exam Code : ST0-093
Exam Name : Symantec Data Loss Prevention 10.5 (STS)
Questions and Answers : 132 Q & A
Updated On : Click to Check Update
PDF Download Mirror : ST0-093 Brain Dump
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ST0-093 Questions and Answers

Pass4sure ST0-093 Dumps with Real Questions & Practice Test


Which feature is a key benefit of on-screen notification?

  1. uses on-screen notification in different languages

  2. educates the user about the violation that has occurred

  3. stops the movement of data that violates policies

  4. notifies the user that the Endpoint Agent is active

Answer: D


Which two components perform a scan of a workstation? (Select two.)

  1. Endpoint Server

  2. DLP Agent

  3. Network Prevent

  4. Enforce Server

  5. Network Monitor

Answer: A, B


Which Network Protect feature is a Data Loss Prevention administrator unable to configure?

  1. ability to restore files

  2. location of the file marker

  3. location of quarantined files

  4. content of the file marker

Answer: B


A Data Loss Prevention administrator needs to modify a policy to a Network Discover scan that has already started. For the remaining shares, files larger than 100 MB need to be ignored. How should this be accomplished?

  1. pause the scan, edit the policy, and start the scan

  2. stop the scan, edit the policy, and restart the scan

  3. modify the policy, the scan will be updated automatically

  4. create a new scan with the updated policy and start the scan

Answer: A


What is one function of a Network Discover scanner?

  1. It scans an organization's network to identify Network Discover targets.

  2. It collects content and metadata from a repository.

  3. It sends collected content to the Enforce Server for processing.

  4. It specifies the types of repositories that can be scanned.

Answer: B


How and when is a solution pack installed?

  1. run SolutionPackInstaller after installing the Enforce Server

  2. run SolutionPackInstaller after installing the database

  3. import the solution pack from the user interface (UI) after logging in to the console for the first time

  4. copy the solution pack into the bin directory on the Enforce Server after installation

Answer: A


When and how is the license for Symantec Data Loss Prevention 10.5 applied during installation?

  1. move the license file to the bin directory after installation

  2. copy and paste the license key when prompted during the installation

  3. upload the license file when prompted by the installer

  4. copy and paste the license key after logging in to the console for the first time

Answer: C


When installing an Endpoint Server, at which point does it register with the Enforce Server?

  1. after installation, the Endpoint Server automatically registers itself with the Enforce Server

  2. after the first Endpoint Agent connects with the Endpoint Server

  3. after adding the server from within the Enforce user interface (UI)

  4. after restarting the Enforce and Endpoint Servers

Answer: C


Which database does Symantec Data Loss Prevention 10.5 support for incident and policy storage?

  1. Microsoft SQL only

  2. Oracle and Microsoft SQL

  3. Oracle only

  4. any database that supports JDBC

Answer: C


When configuring DLP Agents, what does the File Recovery Area Location setting determine?

  1. the securefilestore of incidents and data while agents are offline

  2. the location of files quarantined through Endpoint Discover scans

  3. the temporary backup location of blocked files

  4. the location of files for redeployment or upgrade of agents

Answer: C


What is the main benefit of installing and using the Symantec Management Platform for managing DLP Agents?

  1. the ability to view agent events

  2. the ability to view the health status of the agents

  3. the ability to reconfigure the agent filters

  4. the ability to easily manage agents remotely

Answer: D


Which incidents appear in the Network Incident List when the Network Prevent Action filter is set to "Modified"?

  1. incidents in which confidential content was removed from an SMTP email

  2. incidents in which an SMTP email was changed to include a specified header

  3. incidents in which confidential content was removed from a Web mail

  4. incidents in which confidential content resulted in a blocked Web mail

Answer: B


Which two fallback options are available for a Network Prevent: Remove HTTP/HTTPS Content response rule? (Select two.)

  1. determining a secondary site for posts

  2. blocking content from being posted

  3. sending to an encryption gateway

  4. sending a notification email

  5. allowing content to be posted

Answer: B, E

Symantec ST0-093 Exam (Symantec Data Loss Prevention 10.5 (STS)) Detailed Information

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Validate technical knowledge and competency by becoming a Symantec Certified Specialist (SCS) based on your specific area of Symantec technology expertise. To achieve this level of certification, candidates must pass one proctored SCS exam based on a combination of Symantec training material, commonly referenced product documentation, and real-world job scenarios.
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The Symantec Certification Program provides rigorous, objective assessments of Symantec technical expertise through securely proctored, computer-based, multiple-choice exams (based on real-world job tasks). The program validates the skills and technical competencies necessary for Symantec professionals to efficiently implement, administer, and maintain their data protection, high availability, and security environments utilizing Symantec solutions.
Successful completion of the programs’ current requirements will result in the achievement and reward of either a Symantec Certified Specialist (SCS) or Symantec Certified Professional (SCP) certificate.
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Symantec End Users, Customers, Employees, and Partners (optional). Although each product varies in complexity and depth, all certification exams are created specifically for customers and cover core elements measuring technical knowledge against factors such as installation, configuration, deployment, product management & administration, and day-to-day maintenance. While certification is optional for partners and employees, certification is not a requirement of the Symantec Partner Program and does not count toward program classification.
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Symantec certified candidates and their companies have the ability to gain industry recognition, competitive differentiation, greater productivity & results, increased user community satisfaction, and a tangible measure of their education investment.
Did you know that 76% of candidates and recruiters verified that Symantec Certification was discussed as part of the hiring process? Certification can open the door to increased visibility, better opportunities and new jobs in your industry. In today’s highly competitive environment, certification differentiates you as a professional who is serious about applied learning, making you an asset to a prospective employer. Read about the benefits of Certification for an Individual and Employer.
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End user certification does NOT count toward Partner Program requirements. To learn more view this FAQ sheet (PDF).
Is my Clearwell certification still valid?
See below for details to learn about the acquisition of Clearwell:
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See below for details to learn about the legacy acquisition of PGP:
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How are passing scores established?
Training and Education
The exams are computer-based and delivered at Pearson VUE testing centers. Pearson VUE provides computer-based testing for information technology, academic, government and professional testing programs around the world. Pearson VUE provides a full suite of services from test development to data management, and delivers exams through the world’s most comprehensive and secure network of Test Center Locations in 175 countries. Pearson VUE is a business of Pearson (NYSE: PSO; LSE: PSON), the international media company, whose businesses include the Financial Times Group, Pearson Education and the Penguin Group.
Are exams published on the same schedule worldwide?
Exams will be available on the same schedule worldwide in English at Pearson VUE. Translations will be determined on a country-by-country basis.
How do I register and pay for a Symantec certification exam?
To register for a Symantec certification exam, login or create a Symantec CertTracker account. Exam fees are payable by credit card or by voucher. View the step-by-step instructions on how to register.
View the step-by-step instructions on how to purchase exam vouchers.
How much does it cost to take an exam?
The fee for a standard released Certification exam is $225 USD (or your country’s currency equivalent).
Symantec reserves the right to change exam fees at any time. Always check Pearson’s website to verify exams costs, schedules, and locations.
What is the format of the exams?
Exams are delivered in multiple-choice format, with each having approximately 65-100 questions. It’s common for the exams to contain exhibits/graphics. Exhibits/graphics are shown directly above the question.
How much time is allowed to take an exam?
Allotted exam time varies by exam length. It typically takes one minute to complete each exam question.
How will I be notified that I have passed an exam?
Pearson VUE provides you with instant results at the completion of your exam. A score report will be printed and given to you before you leave the testing center. Candidates are also able to view exam progress by logging into CertTracker.
How will Symantec be notified that I have passed an exam?
Symantec receives candidate exam results daily via file transfers from Pearson VUE to CertTracker Be sure you keep your personal information in your CertTracker profile up-to-date so that you receive proper credit for exams passed and certifications earned.
What score must I achieve to pass an exam?
Passing scores vary by exam. For more information on specific certifications in each category, please see the certification exam details within your selected product solution training path.
Who sees my exam score(s)?
You, Symantec, and your company (if you designate).
If I do not pass an exam, can I find out which questions I got wrong?
No. Symantec maintains this policy to ensure security over the exam questions.
How many times can I take an exam, is there a waiting period, and is there a cost to retake an exam?
If you do not pass an exam on your first attempt, you must wait at least 3 days (72 hours) before a second attempt. If you do not pass an exam on your second attempt, then you must wait at least 2 weeks (14 days) between each additional attempt. If you need to retake an exam that you have already passed in order to fulfill a certification track requirement, you may do so after 3 months. The same cost applies whether you take an exam once or many times.
How can I find out what topics an exam will cover?
Certification requirements, sample exams, exam objectives, recommended training and registration is available for each certification and corresponding exam. For more information on specific certifications in each category, please see the certification exam details within your selected product solution training path.
Are the exams based on current Symantec product versions?
Exams are developed for the current version of the Symantec product release at the time of development. Exams may be updated after significant new versions are released. New exams may not always correspond to the software release schedule.
How do I know what software release version an exam covers?
For more information on specific certifications in each category, please see the certification exam details within your selected product solution training path.
Are practice or sample exams available?
Sample exams are available. Each sample exam consists of multiple-choice items. Some items may have a supporting exhibit which you will be directed to view before answering the item. The sample exams are not timed, however, you should attempt to complete them as quickly as you can. Certification requirements, sample exams, exam objectives, study guides, recommended training, and registration is available for each certification and corresponding exam. For more information on specific certifications in each category, please see the certification exam details within your selected product solution training path.
Why does Symantec list a range of questions for exams?
Symantec regularly conducts statistical analyses of certification exam results for exam maintenance purposes. In doing so, Symantec publishes a range of questions per exam to account for “unscored” questions. In order to ensure the value of the Symantec certification program, Symantec routinely updates exams with new questions on an unannounced basis. Those new questions are initially delivered as “unscored” so that Symantec can evaluate the performance in the field/on the released exam. The “unscored” questions do not count towards your passing score and additional time is already incorporated into the total exam duration to answer these questions.
Symantec also regularly updates exam questions where the actual number of questions per exam may vary from time to time as these unannounced updates occur.
How are the exams developed?
Symantec end users, both internally and in the field, are studied to define the job performance requirements. The results determine the minimum level of competence required for the defined job performance and is tested in the exams. Symantec follows industry standards for “high stakes” exam development.
How are passing scores established?
Although it is intuitive to think that an appropriate passing score for an examination should be 70 or 75 percent correct based on personal experiences taking classroom tests, these arbitrary values may not reflect the performance level expected of the “minimally qualified candidate” given the difficulty of the test. For example, if the examination is very easy, a passing score of 70 may be too low. However, if the examination is very difficult, this same value may be too high.
Establishing passing scores requires the application of systematic procedures that consider the defined performance level definition of the “minimally qualified candidate” and the difficulty of the examination. Before the final passing scores are established, they are evaluated to ensure that the available validity evidence supports their use for the intended purpose of distinguishing the “minimally qualified candidates” from those who are not yet qualified. This systematic method is used to establish and maintain the fairness, validity and reliability of exams.
In order to ensure the value of the Symantec certification program, Symantec routinely updates exams with new questions. In these cases the passing percentage could change per exam from time to time as these unannounced updates occur
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Pretreatment prognostic components for little ones with hepatoblastoma results from the international Society of Paediatric Oncology (SIOP) examine SIOPEL 1. Eur J melanoma 2000;36:1418-1425. 4. Maibach R, Roebuck D, Brugieres L, et al. Prognostic stratification for toddlers with hepatoblastoma: the SIOPEL journey. Eur J cancer 2012;forty eight:1543-1549. 5. Perilongo G, Maibach R, Shafford E, et al. Cisplatin versus cisplatin plus doxorubicin for general-risk hepatoblastoma. N Engl J Med 2009;361:1662-1670. 6. Knight KR, Kraemer DF, Neuwelt EA. Ototoxicity in babies receiving platinum chemotherapy: underestimating a commonly happening toxicity that might also have an impact on educational and social development. J Clin Oncol 2005;23:8588-8596. 7. Stelmachowicz PG, Hoover BM, Lewis DE, Kortekaas RW, Pittman AL. The relation between stimulus context, speech audibility, and perception for typical-listening to and listening to-impaired babies. J Speech Lang Hear Res 2000;forty three:902-914. eight. Gurney JG, Tersak JM, Ness KK, Landier W, Matthay KK, Schmidt ML. hearing loss, satisfactory of lifestyles, and academic complications in long-term neuroblastoma survivors: a report from the little oness Oncology group. Pediatrics 2007;one hundred twenty(5):e1229-e1236. 9. Boothroyd A. Developmental components in speech consciousness. Int Audiol 1970;9:30-38. 10. Brock PR, Bellman SC, Yeomans EC, Pinkerton CR, Pritchard J. Cisplatin ototoxicity in infants: a pragmatic grading gadget. Med Pediatr Oncol 1991;19:295-300. 11. Knight KR, Chen L, Freyer D, et al. group-large, potential analyze of ototoxicity evaluation in babies receiving cisplatin chemotherapy (ACCL05C1): a report from the infantss Oncology community. J Clin Oncol 2017;35:440-445. 12. Brock PR, Brugieres L, Perilongo G, et al. Cisplatin ototoxicity in little ones with hepatoblastoma: can it's reduced? results from the SIOPEL method group. Pediatr Blood melanoma 2006;47:362-362. abstract. 13. Howell SB, Pfeifle CL, Wung WE, et al. Intraperitoneal cisplatin with systemic thiosulfate coverage. Ann Intern Med 1982;ninety seven:845-851. 14. Pfeifle CE, Howell SB, Felthouse RD, et al. excessive-dose cisplatin with sodium thiosulfate insurance policy. J Clin Oncol 1985;3:237-244. 15. Goel R, Cleary SM, Horton C, et al. impact of sodium thiosulfate on the pharmacokinetics and toxicity of cisplatin. J Natl melanoma Inst 1989;eighty one:1552-1560. sixteen. Neuwelt EA, Brummett RE, Doolittle ND, et al. First facts of otoprotection towards carboplatin-brought about hearing loss with a two-compartment equipment in patients with significant fearful gadget malignancy using sodium thiosulfate. J Pharmacol Exp Ther 1998;286:77-eighty four. 17. Blakley BW, Cohen JI, Doolittle ND, et al. suggestions for prevention of toxicity caused with the aid of platinum-based mostly chemotherapy: assessment and abstract of the annual meeting of the Blood-brain Barrier Disruption program, Gleneden seaside, Oregon, March 10, 2001. Laryngoscope 2002;112:1997-2001. 18. Muldoon LL, Pagel MA, Kroll RA, et al. Delayed administration of sodium thiosulfate in animal models reduces platinum ototoxicity without reduction of antitumor exercise. Clin cancer Res 2000;6:309-315. 19. Muldoon LL, Walker-Rosenfeld SL, Hale C, Purcell SE, Bennett LC, Neuwelt EA. Rescue from improved alkylator-prompted phone death with low molecular weight sulfur-containing chemoprotectants. J Pharmacol Exp Ther 2001;296:797-805. 20. Doolittle ND, Muldoon LL, Brummett RE, et al. Delayed sodium thiosulfate as an otoprotectant towards carboplatin-triggered listening to loss in sufferers with malignant brain tumors. Clin melanoma Res 2001;7:493-500. 21. Neuwelt EA, Pagel MA, Kraemer DF, Peterson DR, Muldoon LL. Bone marrow chemoprotection with out compromise of chemotherapy efficacy in a rat brain tumor mannequin. J Pharmacol Exp Ther 2004;309:594-599. 22. Doolittle ND, Muldoon LL, Culp AY, Neuwelt EA. beginning of chemotherapeutics across the blood-mind barrier: challenges and advances. Adv Pharmacol 2014;71:203-243. 23. Harned TM, Kalous O, Neuwelt A, et al. Sodium thiosulfate administered six hours after cisplatin doesn't compromise antineuroblastoma endeavor. Clin melanoma Res 2008;14:533-540. 24. Erdlenbruch B, Nier M, Kern W, Hiddemann W, Pekrun A, Lakomek M. Pharmacokinetics of cisplatin and relation to nephrotoxicity in paediatric sufferers. Eur J Clin Pharmacol 2001;fifty seven:393-402. 25. Brock PR, Knight KR, Freyer DR, et al. Platinum-brought on ototoxicity in infants: a consensus overview on mechanisms, predisposition, and insurance policy, together with a new overseas Society of Pediatric Oncology Boston ototoxicity scale. J Clin Oncol 2012;30:2408-2417. 26. Brock PR, Koliouskas DE, Barratt TM, Yeomans E, Pritchard J. Partial reversibility of cisplatin nephrotoxicity in toddlers. J Pediatr 1991;118:531-534. 27. Delanaye P, Ebert N, Melsom T, et al. Iohexol plasma clearance for measuring glomerular filtration rate in scientific apply and analysis: a assessment. half 1: a way to measure glomerular filtration cost with iohexol? Clin Kidney J 2016;9:682-699. 28. Otte JB, Pritchard J, Aronson DC, et al. Liver transplantation for hepatoblastoma: effects from the overseas Society of Pediatric Oncology (SIOP) study SIOPEL-1 and review of the world experience. Pediatr Blood melanoma 2004;forty two:seventy four-eighty three. 29. Czauderna P, Otte JB, Aronson DC, et al. guidelines for surgical remedy of hepatoblastoma in the modern era techniques from the Childhood Liver Tumour strategy neighborhood of the foreign Society of Paediatric Oncology (SIOPEL). Eur J melanoma 2005;forty one:1031-1036. 30. Cooper BW, Veal GJ, Radivoyevitch T, et al. A phase I and pharmacodynamic examine of fludarabine, carboplatin, and topotecan in patients with relapsed, refractory, or excessive-possibility acute leukemia. Clin melanoma Res 2004;10:6830-6839. 31. Jarvis IWH, Meczes EL, Thomas HD, et al. therapy-induced carboplatin-DNA adduct ranges in human ovarian tumours in relation to evaluation of adduct size in mouse tissues. Biochem Pharmacol 2012;eighty three:69-77. 32. OBrien pc, Fleming TR. A distinct checking out technique for scientific trials. Biometrics 1979;35:549-556. 33. Zsiros J, Brugieres L, Brock P, et al. Dose-dense cisplatin-primarily based chemotherapy and surgery for little ones with high-risk hepatoblastoma (SIOPEL-four): a prospective, single-arm, feasibility analyze. Lancet Oncol 2013;14:834-842. 34. Freyer DR, Chen L, Krailo MD, et al. results of sodium thiosulfate versus remark on construction of cisplatin-caused listening to loss in children with melanoma (ACCL0431): a multicentre, randomised, controlled, open-label, section three trial. Lancet Oncol 2017;18:63-74. 35. Bouffet E. reducing cisplatin ototoxicity in children: some hope and a lot of questions. Lancet Oncol 2017;18:6-7. 36. Neuwelt EA, Gilmer-Knight k, Lacy C, et al. Toxicity profile of delayed excessive dose sodium thiosulfate in infants treated with carboplatin along with blood-mind-barrier disruption. Pediatr Blood cancer 2006;forty seven:174-182. 37. Brock PR, Yeomans EC, Bellman SC, Pritchard J. Cisplatin therapy in little ones: brief and long-time period morbidity. Br J melanoma Suppl 1992;18:S36-S40. 38. Hoebers FJ, Pluim D, Verheij M, et al. Prediction of treatment outcomes by cisplatin-DNA adduct formation in patients with stage III/IV head and neck squamous cellphone carcinoma, treated by using concurrent cisplatin-radiation (RADPLAT). Int J melanoma 2006;119:750-756. 39. Hoebers FJ, Pluim D, Hart AAM, et al. Cisplatin-DNA adduct formation in sufferers handled with cisplatin-based chemoradiation: lack of correlation between normal tissues and primary tumor. melanoma Chemother Pharmacol 2008;sixty one:1075-1081. forty. Breglio AM, Rusheen AE, Shide ED, et al. Cisplatin is retained in the cochlea indefinitely following chemotherapy. Nat Commun 2017;eight:1654-1654. While it is hard errand to pick solid certification questions/answers assets regarding review, reputation and validity since individuals get sham because of picking incorrectly benefit. ensure to serve its customers best to its assets as for exam dumps update and validity. 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