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Virtusa Consulting Services Interview Questions and Answers

Updated 21 Jan 2025
Popular Designations

Q1. How to reduce setup and hold

Ans.

Reducing setup and hold time requires optimizing timing constraints, minimizing clock skew, and using proper synchronization techniques.

  • Optimize timing constraints by adjusting clock frequencies and paths

  • Minimize clock skew by balancing clock distribution and using clock tree synthesis

  • Use proper synchronization techniques like flip-flops or latches to ensure data stability

  • Consider using multi-cycle paths for critical timing paths

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Q2. How to reduce congestion

Ans.

Congestion can be reduced by improving public transportation, implementing congestion pricing, promoting telecommuting, and creating carpooling incentives.

  • Improve public transportation by expanding routes and increasing frequency

  • Implement congestion pricing to discourage driving during peak hours

  • Promote telecommuting to reduce the number of vehicles on the road

  • Create carpooling incentives such as designated lanes or discounts on tolls

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Q3. How do you place macros

Ans.

Macros can be placed in a document by using the 'Developer' tab in Microsoft Word.

  • Go to the 'Developer' tab in Microsoft Word

  • Click on 'Macros'

  • Select 'Create' to write a new macro or 'Record' to record a series of actions as a macro

  • Name the macro and assign it a shortcut key if desired

  • Click 'OK' to save the macro

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Q4. Difference between EUMDR and MDD

Ans.

EUMDR is the new regulation replacing MDD for medical devices in the EU.

  • EUMDR stands for European Union Medical Device Regulation

  • EUMDR has stricter requirements for clinical evidence and post-market surveillance compared to MDD

  • EUMDR requires a Unique Device Identification (UDI) system for better traceability

  • MDD (Medical Device Directive) was the previous regulation governing medical devices in the EU

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Q5. Input file for Physical Design

Ans.

Input file for Physical Design is a file containing information needed for the physical implementation of a circuit.

  • Input file typically includes information on floorplanning, placement, routing, and timing constraints.

  • Examples of input files for Physical Design include LEF/DEF files, Verilog netlists, and technology libraries.

  • The input file is crucial for generating the layout of the circuit and ensuring its functionality and performance.

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Q6. What is mean by DHF

Ans.

DHF stands for Design History File, which is a compilation of documents that describes the design history of a medical device.

  • DHF is a key document required for medical device manufacturers to demonstrate compliance with regulations.

  • It includes design inputs, outputs, verification, validation, and changes made throughout the design process.

  • Examples of documents included in DHF are design plans, risk analysis, design reviews, and design verification reports.

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Q7. DHF documentation steps

Ans.

DHF documentation steps involve creating, updating, and maintaining Design History Files for medical devices.

  • Create DHF documentation for each medical device design iteration

  • Include design inputs, outputs, verification and validation activities

  • Update DHF as design changes are made

  • Maintain DHF throughout the product lifecycle

  • Ensure DHF is easily accessible for audits and reviews

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Interview Process at Virtusa Consulting Services

based on 3 interviews
2 Interview rounds
Resume Shortlist Round
Technical Round
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