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20+ DHL Supply Chain Interview Questions and Answers

Updated 4 Mar 2025
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Q1. What is Pharmacovigilance, Difference between ADR and ADE, Seriousness criterias, Medical significant meaning, one task was given to tell the chronological order of narrative writing, Regulatory authorities of...

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Q2. 1. Types of dimensions 2. What is the use of staging layer 3. How MDM testing is performed 4. How to find the day if date is given

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Q3. What is the importance of Phase 3 Clinical trials, and what is the document that is signed by Study Subjects to show their agreement to participate willingly in a clinical trial?

Ans.

Phase 3 Clinical trials are crucial for determining the safety and efficacy of a new treatment before it can be approved for public use. Study Subjects sign an Informed Consent document to show their agreement to participate willingly.

  • Phase 3 Clinical trials are the final stage of testing before a new treatment can be approved for public use.

  • These trials involve a larger group of participants to further evaluate the safety and efficacy of the treatment.

  • Study Subjects sign an ...read more

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Q4. What do you mean by Pharmacovigilance role? What are AE and casualty? Authority of CLINIC TRAILS in the world?

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Q5. CLINIC TRAILS? What are ICH GCP GUIDELINES? NAMES OF DICTIONARY OF CLINIC TRAILS AND WHY THEY ARE USED?

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Q6. What are the Key Stakeholders involved in a Clinical trial?

Ans.

Key stakeholders in a clinical trial include sponsors, investigators, participants, regulatory authorities, and ethics committees.

  • Sponsors: Provide funding and resources for the trial

  • Investigators: Conduct the trial and collect data

  • Participants: Individuals who volunteer to participate in the trial

  • Regulatory authorities: Ensure compliance with regulations and guidelines

  • Ethics committees: Review and approve the trial protocol to protect participant rights

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Q7. Why add covariates to a Cox model in a randomized trial

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Q8. Describe organizing tasks based on daily updates. Ensuring data accuracy in Excel/Access. Experience with analytical duties and quality control. Handling discrepancies in data documentation. Demonstrating flexi...

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Q9. 2-What is pharmacokinetics and pharmacodynamics?

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Q10. What survival analysis methods I had used

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Q11. 0.03 p value is significant? Why and how?

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Q12. What was my FDA submission experience

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Q13. differnece between innovator drugs, and generic drugs

Ans.

Innovator drugs are brand-name drugs developed by pharmaceutical companies, while generic drugs are copies of innovator drugs made after the patent expires.

  • Innovator drugs are developed by pharmaceutical companies and have a brand name.

  • Generic drugs are copies of innovator drugs and are usually cheaper.

  • Generic drugs can only be made after the patent for the innovator drug expires.

  • Both innovator and generic drugs must meet the same FDA standards for safety and effectiveness.

  • Ex...read more

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Q14. Phases of clinical trail, knowledge of clinical trail.

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Q15. 13 Principles of ICH GCP E6 R2

Ans.

The 13 Principles of ICH GCP E6 R2 are guidelines for conducting clinical trials in a way that ensures the safety and well-being of participants.

  • Principle 1: Clinical trials should be conducted in accordance with ethical principles.

  • Principle 2: The rights, safety, and well-being of trial subjects are the most important considerations.

  • Principle 3: The available non-clinical and clinical information should support the proposed trial.

  • Principle 4: The trial should be scientifical...read more

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Q16. Estimate at Completion (EAC)

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Q17. Phases of Clinical Trial

Ans.

Phases of Clinical Trial involve different stages of testing a new drug or treatment.

  • Phase 1: Small group, safety and dosage testing

  • Phase 2: Larger group, effectiveness and side effects

  • Phase 3: Even larger group, compare to existing treatments

  • Phase 4: Post-marketing surveillance for long-term effects

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Q18. Phases of clinical trials

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Q19. Experience in flow Cytometry

Ans.

Experience in flow cytometry is essential for this role, as it involves analyzing cells and particles in a fluid stream.

  • Hands-on experience with flow cytometers and related software

  • Ability to design and optimize flow cytometry experiments

  • Knowledge of different flow cytometry applications, such as cell counting, cell sorting, and biomarker analysis

  • Experience in analyzing and interpreting flow cytometry data

  • Troubleshooting skills for flow cytometry instrumentation and data anal...read more

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Q20. Pharmaceutical Experience

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Q21. Phases of clinical trail

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Q22. Clinical trial phases

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Q23. ICH GCP Guidelines

Ans.

ICH GCP guidelines are international standards for the design, conduct, performance, monitoring, auditing, recording, analysis, and reporting of clinical trials.

  • Established by the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH)

  • Provide a unified standard for the European Union, Japan, and the United States

  • Emphasize the protection of human subjects and the quality and reliability of trial data

  • Cover aspects such as ethics...read more

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