Founder and Managing Director
Founder and Managing Director Interview Questions and Answers

Asked in Hendrix Pharmaceuticals

Q. Explain drug discovery process and Regulatory reporting
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

Asked in Hendrix Pharmaceuticals

Q. Explain pharmacology classifications
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

Asked in Hendrix Pharmaceuticals

Q. Glassory of Pv and CR
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.

Asked in Hendrix Pharmaceuticals

Q. ICH-GCP guidelines
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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