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Neha, the video's are very informative and well explained. The initial background music is not pleasant just a suggestion kindly see if it can changed for further video's

Thank you for Information!

Great Explanation Neha, Thanks for sharing the knowledge

Mam you are soo better ❤️

Hi mam I am a B.Pharm graduate with around 4 years of experience in the QA department in the Pharmaceutical industry I want to change to Regulatory could you suggest a road map Please

Very Informative! Thanks Neha

Pls make a video on timeline for variation submission for dcp mrp

How to map NDA ids to NCT ids?

Ma'am how and where we apply for DRA in foreign countries

Hi Neha, I had 6 years experience in regulatory affairs in India.I moved to US in 2021 and I have gap of 4 years for starting job. Now I am confused how to start career in regulatory affairs. Can you guide me on that?

Helpful.. keep updating us.. thank you

Thnks for the information

Please make video from casa

Hi Neha, I have been watching all your video's, well very explained and informative video's. Very Inspiring. Please keep sharing the knowledge.

If in Usfda it's DP patented , and this patent is worldwide or Indian companies can make generic of it.???

Which procedure is applicable for Abbreviated new drugs (Combination drugs) Application. I want to take Marketing authorization for all 27 countries in EU. In this case which procedure is applicable?

Usefull information

Very good explanation.

Hi Neha- Do you have slide deck to provide for your presentations?

make more video

In Japan Regulatory body is PMDA

For veterinary products we want to go through cp is it compulsory?

Really helpful, thank you 😊

Project management certification video

Hai neha you are such a gem please make a vedio on PMP certification course and other certification courses which are imp in Regulatory field

Useful

Thank you mam it will be really helpful for me as fresher💫😊 i

Excellent explanation madam

Wowww thank you so much for this mam,

thanks you so much neha you are legend

Pls tell about novel therapy regulatory requirements

Nice Neha, best research and very professional way of explanation, Thank you. Will wait for your videos on ATMPs, and CAT !..... Greetings from London.

Can u please make vdo related to biologics regulations, and different pathways by usfda nd ema to get approval, Thanks a lot

Hii mam what a wonderful explanation, thanks a lot

pls cover this topic PQMC

Please make a video on PMP certification course😊

The content is great, but please consider removing the background music. It was very distracting and made it difficult to hear what you were saying.

Can you make videos on reporting requirements for combination products?

Hi ma'am. Can a microbiology graduate opt for pharmaceutical regulatory affairs ?

Very helpful. Keep doing what you do

Promo SM

Thank you Ma'am !!

Mam do u have any presentation regarding EU whole regulatory process

Nice Neha... Informative one

Neha good motivation for entry level.

Excellent and informative presentation

Please share about NCE-1 filing details.

Hi Neha, great video thanks for that. It'd will be great if you make a video about project management certificate too. I need your opinion before getting that one. Also CMC video will be amazing as well. I like the way how you explain it so it would be very informative. Thanks