Видео

Nice video. Thanks

Very useful information explained in simple words. Thanks a lot. Please keep making new videos

So informative..

Please make a video on EU variation guidelines. I saw your videos on EU MAA applications, You have explained very well.

Thank you Neha for sharing your knoweldge. I find your videos informative and great thing that they are still short videos. Regarding ADR, I assume you meant when adverse reaction is due to drug or when causal relationship is established.

Hii Neha, thank you very much for a very informative video. Can you share your experience where paying attention to details helped or some fallouts you experienced ? It will be something most of us don't know and there's little info out there

Can you please explain in Hindi

Please make a video on clinical trials for cancer drugs

Mam your videos are very informative and unique No RUclips channel provides such kind of information

Useful

😍

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?