RiskVision Interview Questions and Answers

Changing companies can provide new opportunities for growth and development.

• To seek new challenges and experiences

• To advance career goals

• To improve work-life balance

• To escape a toxic work environment

• To pursue a passion or interest

• To increase salary or benefits

• To relocate to a new city or country

HPLC calibration parameters and procedure ensure accurate and reliable results in High Performance Liquid Chromatography.

• HPLC calibration parameters include flow rate, retention time, peak area, and peak height.

• The calibration procedure involves preparing standard solutions of known concentrations, injecting them into the HPLC system, and plotting calibration curves.

• Flow rate calibration ensures accurate sample delivery and separation efficiency.

• Retention time calibration ens...read more

Reactors are vessels used for chemical reactions. Different types include batch, continuous, stirred tank, and plug flow reactors.

• Batch reactors are used for small-scale production and testing.

• Continuous reactors are used for large-scale production and can operate continuously for long periods of time.

• Stirred tank reactors are used for mixing and heating/cooling of liquids.

• Plug flow reactors are used for reactions that require a long residence time and have a continuous flow ...read more

Validation guidelines are a set of rules and standards used to ensure that a product or process meets its intended requirements.

• Validation guidelines are used in various industries, including pharmaceuticals, medical devices, and software development.

• They typically involve testing and documentation to ensure that a product or process meets regulatory requirements and industry standards.

• Validation guidelines may include requirements for equipment, facilities, personnel, and pr...read more

21 CFR Chapter is a set of regulations issued by the US Food and Drug Administration (FDA) to ensure the safety and effectiveness of drugs and medical devices.

• 21 CFR Chapter regulates the manufacturing, testing, labeling, and marketing of drugs and medical devices in the United States.

• It includes regulations for clinical trials, good manufacturing practices, and post-market surveillance.

• Examples of regulations under 21 CFR Chapter include labeling requirements for prescriptio...read more