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Exam Number : ECSS
Exam Name : EC-Council Certified Security Specialist
Vendor Name : EC-Council
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ECSS test Format | ECSS Course Contents | ECSS Course Outline | ECSS test Syllabus | ECSS test Objectives

Exam Title : EC-Council Certified Security Specialist (ECSS)
Exam ID : ECSS
Exam Duration : 120 mins
Questions in test : 50
Passing Score : 70%
Exam Center : Pearson VUE OR ECC test Center
Real Questions : EC-Council ECSS Real Questions
VCE practice test : EC-Council ECSS Certification VCE Practice Test

Information Security and Networking Fundamentals 9%
- Overview of Information Security Fundamentals
- Understanding Information Security Laws and Regulations
- Overview of Networking Fundamentals
- Overview of OSI and TCP/IP Model
- Understanding Basic Network Security Procedures and Policies
- Overview of Secure Network Protocols

Information Security Threats and Attacks 21%
- Understanding Various Stages of Hacking Cycle
- Understanding Internal Threats (Sniffing, ARP Spoofing, etc.)
- Understanding External Threats (Malware Attacks, Password Cracking, DoS, Session Hijacking, etc.)
- Overview of Different Social Engineering Techniques
- Understanding Various Firewall and IDS Evasion Techniques
- Understanding Various Wireless and VPN Threats
- Understanding Various Web Applications and Network Threats
- Understanding Email Crime

Information Security Controls 23%
- Overview of Identification, Authentication, and Authorization
- Overview of Cryptography and Encryption Algorithms
- Understanding Different Firewall Technologies
- Overview of Intrusion Detection System (IDS)
- Introduction to Data Backup
- Securing Organization Against Various Information Security Attacks

Wireless Network, VPN, and Web Application Security 17%
- Overview of Wireless Networks and Topology
- Understanding Different Types of Wireless Encryption
- Securing Wireless Networks
- Understanding VPN and Protocols Used to Secure VPN
- Introduction to Web Applications and Securing Web Application Against Web Attacks

Ethical Hacking and Pen Testing 1%
- Introduction to Ethical Hacking
- Introduction to Penetration Testing

Incident Response and Computer Forensics Fundamentals 6%
- Overview of Incident Handling and Response Process
- Understand Different Computer Security Incidents and Computer Crimes
- Overview of Computer Forensics Fundamentals
- Understanding Computer Forensics Investigation Methodology

Digital Evidence and File Systems 4%
- Understanding Digital Evidence and Examination Process
- Collecting Digital Evidence from Electronic Devices
- Overview of Different File Systems (Windows, Linux, Mac OS X, and CD-ROM / DVD File Systems)

Windows and Network Forensics 10%
- Understanding Network Forensics Analysis Mechanism
- Understanding Windows Forensics (Collecting Volatile and Non-volatile Information)
- Collecting Metadata and Events Data
- Introduction to Steganography
- Understanding Different Types of Steganography based on Cover Medium

Logs and Email Crime Forensics 6%
- Examining Various Security Logs
- Overview of Event Correlation
- Overview of Email Technology
- Investigating Email Crime and Violation

Investigation Report 3%
- Writing Computer Forensics Report
- Understanding Best Practices for Writing Forensics Report

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EC-Council Security PDF Dumps

replace on Regulatory Submission for Aducanumab within the European Union | ECSS mock test and boot camp

Biogen to are looking for re-examination following CHMP terrible opinion for aducanumab

CAMBRIDGE, Mass., Dec. 17, 2021 (GLOBE NEWSWIRE) -- Biogen Inc. (Nasdaq: BIIB) and Eisai Co., Ltd. (Tokyo, Japan) today announced that the Committee for Medicinal products for Human Use (CHMP) of the ecu drug treatments company (EMA) has adopted a negative opinion on the advertising and marketing Authorization utility (MAA) for aducanumab for the remedy of the early levels of Alzheimer’s ailment referred to as mild cognitive impairment (MCI) because of Alzheimer’s ailment and gentle Alzheimer’s sickness dementia. This decision is aligned to the terrible vogue vote of the committee in November 2021. Biogen will are trying to find a re-examination of the opinion by means of the CHMP.

“For Europeans impacted by using Alzheimer’s disorder, the lack of options to deal with its early tiers is felt daily. The longer they wait, the extra individuals will progress toward greater superior dementia and they may leave out the probability to doubtlessly treat them,” mentioned Priya Singhal, M.D., M.P.H., Head of world safety & Regulatory Sciences and interim Head of research & development at Biogen. “As a part of the re-examination technique, they will are looking for to handle the CHMP’s grounds for refusal, with the aim of making this medication obtainable within the eu. European patients deserve access to imaginitive remedies for Alzheimer’s ailment.”

the ecu fee’s regulations1 permit an applicant to request a re-examination of a CHMP opinion, adopted by using submission of documentation with particular grounds for the request. The Committee has 60 days after receipt of this documentation to re-verify their opinion2.

The MAA blanketed efficacy, safeguard and biomarker facts from a world, multi-analyze scientific development application which covered approximately three,600 sufferers in additional than 20 countries.

In June 2021, the U.S. meals and Drug Administration (FDA) granted accelerated acclaim for ADUHELM® (aducanumab-avwa) one hundred mg/mL injection for intravenous use because the first Alzheimer’s disease remedy to tackle a defining pathology of the ailment by means of reducing amyloid beta plaques in the mind. ADUHELM is also accepted within the United Arab Emirates (UAE).

Story continues

About ADUHELM®(aducanumab-avwa) injection 100 mg/mL solution for intravenous useIn the united states, ADUHELM is indicated for the medicine of Alzheimer’s sickness. medicine with ADUHELM should be initiated in patients with mild cognitive impairment or light dementia stage of disease, the population during which remedy became initiated in scientific trials. There aren't any protection or effectiveness information on initiating treatment at prior or later degrees of the disorder than were studied. This indication is accepted beneath accelerated approval based on discount in amyloid beta plaques observed in sufferers handled with ADUHELM. endured acclaim for this indication can be contingent upon verification of clinical improvement in confirmatory trial(s).

ADUHELM is a monoclonal antibody directed towards amyloid beta. the buildup of amyloid beta plaques in the brain is a defining pathophysiological characteristic of Alzheimer’s disorder. The accelerated approval of ADUHELM has been granted in response to data from medical trials displaying the effect of ADUHELM on reducing amyloid beta plaques, a surrogate biomarker that is reasonably more likely to predict scientific advantage, during this case a reduction in clinical decline.

ADUHELM may cause critical side effects including: Amyloid connected Imaging Abnormalities or “ARIA”. ARIA is a standard aspect impact that doesn't always cause any indicators but may also be critical. despite the fact most individuals won't have indicators, some americans might also have symptoms comparable to: headache, confusion, dizziness, vision changes and nausea. The affected person’s healthcare provider will do magnetic resonance imaging (MRI) scans before and during treatment with ADUHELM to examine for ARIA. ADUHELM can additionally cause serious allergy symptoms. probably the most common facet outcomes of ADUHELM include: swelling in areas of the brain, with or without small spots of bleeding within the brain or on the floor of the mind (ARIA); headache; and fall. patients should still name their healthcare provider for medical tips about aspect effects.

As of October 2017, Biogen and Eisai Co., Ltd. are collaborating on the world co-construction and co-promotion of aducanumab.

Please click right here for U.S. full Prescribing advice, including medication ebook, for ADUHELM.

About Alzheimer’s DiseaseAlzheimer’s sickness is a progressive neurological situation that impairs thinking, memory and independence, leading to untimely dying. The sickness is a growing to be global health crisis, affecting these residing with the sickness and their households. based on the world health company (WHO), greater than 30 million individuals global reside with Alzheimer’s sickness, and the number will grow in the years forward, outpacing the healthcare supplies mandatory to manage it and costing billions of bucks.

Alzheimer’s disorder is characterised by means of alterations in the mind, including the irregular accumulation of toxic amyloid beta plaques, which begins about two decades before sufferers display signs of the disorder. gentle cognitive impairment as a result of Alzheimer’s ailment is without doubt one of the earliest symptomatic ranges of the ailment when indicators start to be greater visible and might be detected and diagnosed.For extra advice about Alzheimer’s disorder, seek advice from

About BiogenAs pioneers in neuroscience, Biogen discovers, develops and grants global resourceful treatment options for americans living with serious neurological ailments in addition to connected therapeutic adjacencies. one of the vital world’s first global biotechnology companies, Biogen became established in 1978 by using Charles Weissmann, Heinz Schaller, Sir Kenneth Murray and Nobel Prize winners Walter Gilbert and Phillip Sharp. today, Biogen has the leading portfolio of drug treatments to treat varied sclerosis, has brought the first approved remedy for spinal muscular atrophy, and is featuring the primary and handiest accepted medication to address a defining pathology of Alzheimer’s disease. Biogen is additionally commercializing biosimilars and specializing in advancing the business’s most diverse pipeline in neuroscience as a way to transform the general of take care of patients in a few areas of high unmet want.

In 2020, Biogen launched a daring 20-year, $250 million initiative to address the deeply interrelated concerns of local weather, fitness and fairness. fit local weather, suit Lives™ goals to dispose of fossil fuels throughout the business’s operations, construct collaborations with well-known institutions to advance the science to enhance human fitness consequences, and aid underserved communities.

The enterprise automatically posts assistance that can be important to buyers on its web page at To study extra, please talk over with and comply with Biogen on social media – Twitter, LinkedIn, facebook, YouTube.

About Eisai Co., Ltd.Eisai Co., Ltd. is a leading international pharmaceutical company headquartered in Japan. Eisai’s company philosophy is according to the human fitness care (hhc) thought, which is to provide first idea to sufferers and their families, and to increase the advantages that health care gives to them. With a worldwide network of R&D facilities, manufacturing sites and advertising subsidiaries, they attempt to know their hhc philosophy by delivering imaginative items to target illnesses with high unmet scientific needs, with a particular focal point in their strategic areas of Neurology and Oncology.

Leveraging the event won from the construction and marketing of a medicine for Alzheimer’s disorder, Eisai aims to set up the “Eisai Dementia Platform.” via this platform, Eisai plans to convey novel merits to those dwelling with dementia and their families via developing a “Dementia Ecosystem,” by means of participating with companions such as clinical organizations, diagnostic building organizations, research organizations and bio-ventures besides inner most insurance companies, finance industries, fitness golf equipment, car makers, agents and care amenities. For greater advice about Eisai Co., Ltd., please talk over with

Biogen secure HarborThis information unlock includes ahead-searching statements, including statements made pursuant to the protected harbor provisions of the inner most Securities Litigation Reform Act of 1995, the knowledge scientific effects of ADUHELM; the advantage benefits, defense and efficacy of ADUHELM; Biogen’s strategy and plans; capabilities of, and expectations for, Biogen’s commercial enterprise and pipeline classes, including ADUHELM; planning and timing for the commercial launch of, and entry to, ADUHELM; predicted manufacturing, distribution, and provide of ADUHELM; the medication of Alzheimer’s disease; the anticipated advantages and skills of Biogen’s collaboration preparations with Eisai; the skills of Biogen’s business company and pipeline courses, including ADUHELM; and risks and uncertainties associated with drug development and commercialization. These statements may be recognized by using words corresponding to “goal,” “anticipate,” “trust,” “may,” “estimate,” “expect,” “forecast,” “intend,” “may additionally,” “plan,” “viable,” “knowledge,” “will,” “would” and other phrases and terms of an identical meaning. Drug development and commercialization contain a high diploma of possibility, and handiest a small number of research and building courses influence in commercialization of a product. consequences in early stage clinical trials may additionally no longer be indicative of full consequences or outcomes from later stage or greater scale clinical trials and don't be certain regulatory approval. you should not vicinity undue reliance on these statements or the scientific information presented.

These statements contain risks and uncertainties that might cause exact outcomes to differ materially from those mirrored in such statements, together with, without issue, uncertainty of success within the development and commercialization of ADUHELM; risks relating to the launch of ADUHELM, including preparedness of healthcare suppliers to deal with sufferers, the skill to attain and preserve sufficient repayment for ADUHELM, and different unexpected difficulties or hurdles; unexpected considerations that might also come up from additional facts or evaluation bought during medical trials; the incidence of adverse safeguard activities, restrictions on use, or product liability claims; regulatory authorities might also require more information or additional reports, or may additionally fail or refuse to approve or may additionally extend approval of Biogen’s drug candidates, together with ADUHELM; hazards of surprising expenses or delays; the chance of different sudden hurdles; dangers relating to funding in their manufacturing skill; issues with their manufacturing procedures; failure to protect and implement their records, highbrow property, and other proprietary rights and uncertainties relating to intellectual property claims and challenges; third party collaboration risks; hazards linked to existing and capabilities future healthcare reforms; dangers relating to the distribution and sale through third parties of counterfeit or unfit models of their products; and the direct and indirect influences of the continued COVID-19 pandemic on their business, effects of operations and economic situation. The foregoing sets forth many, however no longer all, of the factors that could cause genuine effects to vary from Biogen’s expectations in any forward-looking statement. traders should believe this cautionary commentary as well as the chance elements identified in Biogen’s most contemporary annual or quarterly report and in other studies Biogen has filed with the U.S. Securities and change fee. These statements are in keeping with Biogen’s latest beliefs and expectations and communicate simplest as of the date of this news free up. Biogen doesn't undertake any obligation to publicly replace any forward-searching statements, no matter if as a result of new suggestions, future trends or in any other case.

MEDIA CONTACT(S):BiogenAshleigh Koss+ 1 908 205

INVESTOR CONTACT(S):BiogenMike Hencke+1 781 464

Eisai Co., Ltd.Public family members DepartmentTEL : +81 (0)3 3817 5120

Eisai Co., Ltd.Investor relations DepartmentTEL: +eighty one-(0)70-8688-9685


1 EC guiding principle: regulation (EC) No 726/2004 OF the eu PARLIAMENT AND OF THE COUNCIL of 31 March 2004 (https://eur-lex.europa.ecu/LexUriServ/ European medicines company, Procedural information on the Re-Examination of CHMP Opinions, 2009. https://www.ema.europa.european/en/files/regulatory-procedural-guiding principle/procedural-advice-re-examination-chmp-opinions_en.pdf

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