Founder and Managing Director

Founder and Managing Director Interview Questions and Answers

Updated 8 Nov 2023

Q1. Explain drug discovery process and Regulatory reporting

Ans.

Drug discovery process involves identifying potential drug candidates and testing them for safety and efficacy. Regulatory reporting ensures compliance with laws and regulations.

  • Drug discovery process starts with target identification, followed by lead compound identification, optimization, preclinical testing, and clinical trials.

  • Regulatory reporting involves submitting data to regulatory authorities for approval to market a drug.

  • Regulatory reporting also includes post-marke...read more

Q2. Explain pharmacology classifications

Ans.

Pharmacology classifications categorize drugs based on their mechanism of action, therapeutic use, and chemical structure.

  • Pharmacological classifications categorize drugs based on their mechanism of action

  • Therapeutic classifications group drugs based on their primary use or indication

  • Chemical classifications categorize drugs based on their chemical structure

  • Examples include beta-blockers (mechanism of action), antibiotics (therapeutic use), and benzodiazepines (chemical struc...read more

Q3. Glassory of Pv and CR

Ans.

PV stands for photovoltaic and CR stands for conversion rate.

  • PV refers to the technology that converts sunlight into electricity.

  • CR is the measure of how effectively a website or landing page converts visitors into leads or customers.

  • PV systems can include solar panels, inverters, and batteries.

  • CR can be improved through A/B testing, optimizing landing pages, and improving user experience.

Q4. ICH-GCP guidelines

Ans.

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

  • ICH-GCP stands for International Conference on Harmonisation - Good Clinical Practice

  • These guidelines provide a unified standard for the European Union, Japan, and the United States to facilitate the mutual acceptance of clinical data by the regulatory authorities

  • They ensure the protection of the rights, safety, and w...read more

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