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MuleSoft Certified Platform Architect - Level 1 Exam Dumps

MCPA-Level-1 Exam Format | Course Contents | Course Outline | Exam Syllabus | Exam Objectives

Exam Code: MCPA Level 1

Exam Name: MuleSoft Certified Platform Architect - Level 1

Format: Multiple-choice, closed book, proctored, online

Length: 60 questions

Duration: 120 minutes (2 hours)

Pass score: 70%

Language: English

A MuleSoft Certified Platform Architect should be able to define and be responsible for an organization’s Anypoint Platform strategy. The MCPA – Level 1 exam validates that an architect has the required knowledge and skills to direct the emergence of an effective application network out of individual integration solutions following API-led connectivity across an organization using Anypoint Platform. Certified candidates should be able to:

- Optimize and shape the Anypoint Platform deployment in the specific organizational context, working with business, infrastructure, InfoSec, and other teams.

- Define how Anypoint Platform is used in conjunction with other tools and applications in the organization.

- Define the usage of Anypoint Platform and the corresponding organizational and process changes needed to help the platform be sustainable.

- Provide guidance and drive the creation of standards, reusable assets, and automation required for scale and multi-LoB adoption.

Details;

- Explaining application network basics

- Establishing organizational and platform foundations

- Designing and sharing APIs

- Designing APIs using System, Process, and Experience Layers

- Governing APIs on Anypoint Platform

- Architecting and deploying API implementations

- Deploying API implementations to CloudHub

- Meeting API quality goals

- Monitoring and analyzing application networks

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MCPA-Level-1
MuleSoft Certified Platform Architect � Level 1
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QUESTION 50
When must an API implementation be deployed to an Anypoint VPC?
A. When the API implementation must invoke publicly exposed services that are deployed outside of CloudHub in a customer-managed AWS instance.
B. When the API implementation must be accessible within a subnet of a restricted customer-hosted network that does not allow public access.
C. When the API implementation must be deployed to a production AWS VPC using the Mule Maven pluginD. When the API implementation must write to a persistent Object Store
Correct Answer: A
QUESTION 51
What is true about API implementations when dealing with legal regulations that require all data processing to be performed within a certain jurisdiction (such as in the USA or the EU)?
A. They must avoid using the Object Store as it depends on services deployed ONLY to the US East region.
B. They must use a jurisdiction-local external messaging system such as Active MQ rather than Anypoint MQ.
C. They must be deployed to Anypoint Platform runtime planes that are managed by Anypoint Platform control planes, with both planes in the same jurisdiction.
D. They must ensure ALL data is encrypted both in transit and at rest.
Correct Answer: C
Reference: https://docs.mulesoft.com/eu-control-plane/
QUESTION 52 An API has been updated in Anypoint Exchange by its API producer from version 3.1.1 to 3.2.0 following accepted semantic versioning practices and the changes have been communicated via the
API's public portal.
The API endpoint does NOT change in the new version.
How should the developer of an API client respond to this change?
A. The update should be identified as a project risk and full regression testing of the functionality that uses this API should be run.
B. The API producer should be contacted to understand the change to existing functionality.
C. The API producer should be requested to run the old version in parallel with the new one.
D. The API client code ONLY needs to be changed if it needs to take advantage of new features.
Correct Answer: D
Explanation
Reference: https://docs.mulesoft.com/exchange/to-change-raml-version
QUESTION 53
Mule applications that implement a number of REST APIs are deployed to their own subnet that is inaccessible from outside the organization.
External business-partners need to access these APIs, which are only allowed to be invoked from a separate subnet dedicated to partners - called Partner-subnet. This subnet is accessible from the public internet, which allows these external
partners to reach it.
Anypoint Platform and Mule runtimes are already deployed in Partner-subnet. These Mule runtimes can already access the APIs.
What is the most resource-efficient solution to comply with these requirements, while having the least impact on other applications that are currently using the APIs?
A. Implement (or generate) an API proxy Mule application for each of the APIs, then deploy the API proxies to the Mule runtimes.
B. Redeploy the API implementations to the same servers running the Mule runtimes.
C. Add an additional endpoint to each API for partner-enablement consumption.
D. Duplicate the APIs as Mule applications, then deploy them to the Mule runtimes.
Correct Answer: A
QUESTION 54
When could the API data model of a System API reasonably mimic the data model exposed by the corresponding backend system, with minimal improvements over the backend system's data model?
A. When there is an existing Enterprise Data Model widely used across the organization.
B. When the System API can be assigned to a bounded context with a corresponding data model.
C. When a pragmatic approach with only limited isolation from the backend system is deemed appropriate.
D. When the corresponding backend system is expected to be replaced in the near future.
Correct Answer: A
QUESTION 55
Refer to the exhibit.
An organization uses one specific CloudHub (AWS) region for all CloudHub deployments.
How are CloudHub workers assigned to availability zones (AZs) when the organization's Mule applications are deployed to CloudHub in that region?
A. Workers belonging to a given environment are assigned to the same AZ within that region.
B. AZs are selected as part of the Mule application's deployment configuration.
C. Workers are randomly distributed across available AZs within that region.
D. An AZ is randomly selected for a Mule application, and all the Mule application's CloudHub workers are assigned to that one AZ.
Correct Answer: D
QUESTION 56 What is most likely NOT a characteristic of an integration test for a REST API
implementation?
A. The test needs all source and/or target systems configured and accessible.
B. The test runs immediately after the Mule application has been compiled and packaged.
C. The test is triggered by an external HTTP request.
D. The test prepares a known request payload and validates the response payload.
Correct Answer: D
QUESTION 57 An API implementation is updated. When must the RAML definition of the API
also be updated?
A. When the API implementation changes the structure of the request or response messages.
B. When the API implementation changes from interacting with a legacy backend system deployed on-premises to a modern, cloud-based (SaaS) system.
C. When the API implementation is migrated from an older to a newer version of the Mule runtime.
D. When the API implementation is optimized to improve its average response time.
Correct Answer: D
QUESTION 58 What Mule application can have API policies applied by Anypoint Platform to the endpoint exposed by that
Mule application? A. A Mule application that accepts requests over HTTP/1x.
B. A Mule application that accepts JSON requests over TCP but is NOT required to provide a response.
C. A Mule application that accepts JSON requests over WebSocket.
D. A Mule application that accepts gRPC requests over HTTP/2
Correct Answer: D
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MCPA-Level-1 1 testing

MCPA-Level-1 1 testing :: Article Creator

the use of IEC 60601-1-2 for testing scientific gadgets

For effective EMC trying out, scientific manufacturers may still personalize a standards doc such as IEC 60601-1-2.

because the electromagnetic spectrum becomes increasingly congested and electronic devices proliferate, making certain electromagnetic compatibility (EMC) among electrical and digital equipment becomes a important challenge.

guaranteeing EMC is a a must have situation for groups producing electrical and digital medical instruments. These forms of contraptions ought to perform as intended and not intrude with different equipment, or the consequences could be catastrophic. For scientific producers, making bound that devices meet EMC necessities is not handiest a advertising necessity, but additionally a societal concern.

There are a number of EMC specifications, however none of them by myself will supply appropriate trying out guidelines for extremely really good clinical devices. To cut back confusion and make sure that instruments may be confirmed as it should be, scientific manufacturers should use an current typical as a e-book for developing a personalized testing plan.

IEC 60601-1-2

The international Electrotechnical commission (IEC) is a global body that promotes foreign standardization in electronics. In 1993 it launched the 60601-1-2 commonplace, "scientific Electrical equipment—part 1: accepted requirements for safety, amendment No. 2. Collateral common: Electromagnetic Compatibility necessities and exams."1

The IEC 60601 regular offers a superior foundation for medical gadget testing. however they are tremendously new, the IEC 60601-1-2 requirements have rapidly turn into identified throughout the realm and are instrumental in checking out to the eu medical gadgets Directive. businesses such as the American country wide specifications Institute (ANSI) use the IEC 60601 ordinary as a foundation for their own necessities.

This document specifies desirable stages for immunity and refers to other files to specify emission degrees. however, these levels might also no longer be strict enough to make sure that machine will operate as supposed. manufacturers should use the IEC standards as a e book but tailor them to provide product-selected limits.

verify requirements and bounds

The IEC 60601-1-2 ordinary specifies look at various limits for emissions, immunity, electrostatic discharge (ESD), radiated radio-frequency electromagnetic fields, bursts, and surges.

Emissions. equipment should still conform to the conducted and radiated emissions requirements of the overseas special Committee on Radio Interference (CISPR). Classification of equipment for this intention is based on meant use and determined by the brand.

device may be confirmed for emissions at a standard check site, which might encompass a turntable and floor plane, and have general attenuation curves. equipment may also be tested after it has been installed on the clients' premises. it is recognized that scientific gadget may additionally have wonderful installation considerations and that category testing of the installation is the best useful solu-tion to display compliance to the requirements.

producers should still confer with CISPR eleven for the applicable requirements and amplitude levels once the class of machine and check area has been decided.2

presently, there are no requirements for low-frequency emissions, harmonic distortion, and voltage fluctuations, however some machine that operate in an intermittent mode will need to meet selected variations of the CISPR 14 click on requirements.three

CISPR eleven covers a frequency latitude from 150 kHz to 18 GHz. conducted emissions for low- and medium-voltage power mains (100–415 V) are carried out from 150 kHz to 30 MHz. The frequency latitude for radiated emissions is from one hundred fifty kHz to 18 GHz. counting on the type and use of the machine, numerous frequency levels may well be defined. most effective the magnetic part of the radiated box is measured from one hundred fifty kHz to 30 MHz. Above 30 MHz, each the vertical and horizontal add-ons of the box ought to be measured.

Amplitude limits in well-known are established to protect the public broadcast services, not for machine that may have to function in close proximity to sensitive clinical gadget.

The specification also refers to frequencies distinctive by the international Telecommunication Union: 2450 MHz for industrial, 5800 MHz for scientific, and 24,one hundred twenty five MHz for medical gadget.

Immunity. normal immunity requirements are unique in IEC 60601-1-2. look at various tiers are given and examine methods are in accordance with the IEC 801 series of immunity necessities. If lower limits are justified, accompanying files may still explain this and describe any action that allows you to, as a outcome, be taken by means of the installer or user.

Accompanying files should still encompass guidelines for avoiding or deciding on and resolving adverse electromagnetic effects. If using the machine is proscribed on account of its electromagnetic characteristics, significant restrictions should be described in the accompanying documents.

Compliance with the necessities may still be checked by verifying that the equipment continues to operate its meant services as targeted by means of the manufacturer or fails without growing a security hazard.

ESD. equipment may still conform to the present version of IEC 801-2.four A restrict of 3 kV applies for direct contact discharge to all conductive purchasable ingredients and coupling planes. A restrict of 8 kV applies for air discharge to nonconductive accessible ingredients.

Radiated Radio-frequency Electromagnetic Fields. machine may still conform to the IEC 801-3 requirements, that are being up to date.5 A limit of 3 V/m should be used over a frequency range of 26 MHz to 1 GHz. other ranges apply to equipment utilized in shielded locations, such as x-ray and MRI amenities. The three-V/m requirement is lowered in percentage to the expanding protective effectiveness of the vicinity.

There are provisions for amplitude modulation of the signal, based upon the passband of the equipment beneath look at various (EUT). If the EUT does not have a passband, the sign should be amplitude modulated at 1 kHz.

Bursts. examine methods and instruments designated in IEC 801-4 may still be followed.6 A 1-kV degree applies to equipment related to the energy line with a plug. For completely put in equipment, a degree of 2 kV applies. Interconnecting traces longer than three m should still be able to stand up to a 0.5-kV surge.

Surges. check strategies and contraptions distinct in IEC 801-5, which is at the moment still beneath consideration, should still be followed.7 power strains should still meet ranges of 1 kV for differential mode and a pair of kV for ordinary mode. sign strains need not be validated, and telecom strains are coated by using different specifications. Ring wave and damped sinusoid checks don't seem to be relevant.

There are future provisions for voltage dips, short interruptions, and voltage diversifications on vigor strains, in addition to for performed immunity above 9 kHz and magnetic box immunity.

customized requirements

producers of electrical and digital gadget for any use are recognizing the want for necessities that be sure compatibility among gadget. scientific electronics manufacturersalso appreciate that such popular necessities aren't always appropriate; they may be too extreme, or, even worse, now not extreme enough to protect their items. To diminish confusion and to make certain that examine specifications may be acceptable, clinical producers should still use an existing document equivalent to IEC 60601-1-2 as a basis for growing their own product-specific specifications.

REFERENCES

1. "clinical Electrical device part 1: standard necessities for security, change No. 2. Collateral standard: Electromagnetic Compatibility—necessities and assessments," Geneva, IEC, Bureau central de la commission Electrotechnique, 1st ed, 1993.

2. foreign particular Committee on Radio Interference, CISPR e-book 11, "Limits and strategies of size of Radio Interference characteristics of commercial, Scientific and clinical (ISM) Radio Frequency machine (excluding Surgical Diathermy equipment)," Geneva, IEC, 2nd ed, 1990.

three. international special Committee on Radio Interference, CISPR ebook 14, "Limits and methods of Measurements of Radio Interference traits of household Electrical appliances, portable equipment and identical Electrical equipment," Geneva, IEC, 2nd ed, 1985.

four. IEC 801-2, "Electromagnetic Compatibility for Industrial-manner measurement and control device, part 2: Electrostatic Discharge necessities," Geneva, IEC, 2nd ed, 1991.

5. IEC 801-three, "Electromagnetic Compatibility for Industrial-process size and control equipment, part three: Radiated Electromagnetic box requirements," Geneva, IEC, 1st ed, 1984, third impression, 1991.

6. IEC 801-4, "Electromagnetic Compatibility for Industrial-system dimension and handle gadget, part 4: Electrical quick Transient/Burst requirements," Geneva, IEC, 1st ed, 1988.

7. IEC 801-5, "Electromagnetic Compatibility for Industrial-method measurement and handle machine, half 5: Surge Immunity requirements," draft, Geneva, IEC, July 1992.

Gary Fenical is a senior EMC engineer with Instrument Specialties company, Inc. (Delaware Water gap, PA).

Illustration by Sarah Whitehead

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