HCLTech Regulatory Affairs Associate Interview Questions and Answers

Q1. Explain your work that you mentioned in CV
Ans. 
I have experience in preparing regulatory submissions, ensuring compliance with regulations, and communicating with regulatory agencies.
• Prepared regulatory submissions for new products and changes to existing products

• Ensured compliance with relevant regulations and guidelines

• Communicated with regulatory agencies to address any issues or questions

• Reviewed and updated regulatory documentation as needed
Answered by AI
Add your answer
Q2. Any tricky question relevant to their field
Add your answer

Q1. Clinical trials type
Add your answer
Q2. What is regulatory affairs
Ans. 
Regulatory affairs involve ensuring compliance with laws and regulations related to products and services.
• Regulatory affairs involve interpreting and implementing regulations set by government agencies.

• They ensure products meet safety and quality standards before being marketed.

• Regulatory affairs professionals work to obtain and maintain product approvals and registrations.

• They also monitor and report any changes in re...read more
Answered by AI
Add your answer

Q1. Job location in which state
Ans. 
The job location is in California.
• Job location is in California

• Specific city within California may vary

• California is known for its strict regulatory environment

• Many pharmaceutical and biotech companies are based in California
Answered by AI
Add your answer

General apti tests were there, you can try NQT test samples in TCS carer NQT website

Q1. Project related and technical questions
Add your answer
Q2. Regulatory Affairs, CTA
Add your answer
Q3. Clinical trials
Add your answer
Q4. Devolopment of new drugs
Add your answer
Q5. NDA, IND, ANDA, Health authority names
Add your answer