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@pranamks5104 16 күн бұрын
Useful
@pharmajobalert2933 Ай бұрын
😍
@vanithas6582 Ай бұрын
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
@vanithas6582 Ай бұрын
Thank you for Information!
@vanithas6582 Ай бұрын
Great Explanation Neha, Thanks for sharing the knowledge
@GPAT..24 Ай бұрын
Mam you are soo better ❤️
@sakthikumarand339 Ай бұрын
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
@shyammahajan4098 Ай бұрын
Very Informative! Thanks Neha
@priyam-xm1wj Ай бұрын
Pls make a video on timeline for variation submission for dcp mrp
@TrishaDas-xd5ew Ай бұрын
How to map NDA ids to NCT ids?
@user-nl6lc5vi7g Ай бұрын
Ma'am how and where we apply for DRA in foreign countries
@shilpagcp Ай бұрын
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?
@shivarajkumbar3865 Ай бұрын
Helpful.. keep updating us.. thank you
@shalinijha6890 2 ай бұрын
Thnks for the information
@regulatoryvision7926 2 ай бұрын
Please make video from casa
@vanithas6582 2 ай бұрын
Hi Neha, I have been watching all your video's, well very explained and informative video's. Very Inspiring. Please keep sharing the knowledge.
@maitighar1757 2 ай бұрын
If in Usfda it's DP patented , and this patent is worldwide or Indian companies can make generic of it.???
@AeshaPatel-gz6io 2 ай бұрын
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?
@Anilkumar-ww9gu 2 ай бұрын
Usefull information
@ashishkokate7862 3 ай бұрын
Very good explanation.
@roxananikoui3810 3 ай бұрын
Hi Neha- Do you have slide deck to provide for your presentations?
@tusharvashisth5102 3 ай бұрын
make more video
@mounikaadla7227 3 ай бұрын
In Japan Regulatory body is PMDA
@jagdishchavan3630 3 ай бұрын
For veterinary products we want to go through cp is it compulsory?
@Aamenaaaa 4 ай бұрын
Really helpful, thank you 😊
@pratikjagtap8267 4 ай бұрын
Project management certification video
@omkarprabhumu7662 4 ай бұрын
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
@hariomdixit7754 4 ай бұрын
Useful
@PremKumar-ct7rj 5 ай бұрын
Thank you mam it will be really helpful for me as fresher💫😊 i
@pharmacamp 4 ай бұрын
Most welcome 😊
@gangadharm1983 5 ай бұрын
Excellent explanation madam
@pharmacamp 5 ай бұрын
Thanks
@sambhajimasal4248 6 ай бұрын
Wowww thank you so much for this mam,
@pharmacamp 5 ай бұрын
Most welcome 😊
@hirendayani6523 6 ай бұрын
thanks you so much neha you are legend
@sharmilam8496 6 ай бұрын
Pls tell about novel therapy regulatory requirements
@bapufromUK 6 ай бұрын
Nice Neha, best research and very professional way of explanation, Thank you. Will wait for your videos on ATMPs, and CAT !..... Greetings from London.
@pharmacamp 5 ай бұрын
Thank you :-)
@sambhajimasal4248 6 ай бұрын
Can u please make vdo related to biologics regulations, and different pathways by usfda nd ema to get approval, Thanks a lot
@pharmacamp 5 ай бұрын
We will cover in the future videos. Thanks.
@sambhajimasal4248 6 ай бұрын
Hii mam what a wonderful explanation, thanks a lot
@pharmacamp 5 ай бұрын
Thank you :-)
@shivangsaxena7723 7 ай бұрын
pls cover this topic PQMC
@bishwamitrakhoirom9244 7 ай бұрын
Please make a video on PMP certification course😊
@piranha10 7 ай бұрын
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.
@rubinasharma3134 8 ай бұрын
Can you make videos on reporting requirements for combination products?
@ROJASDTECHY 8 ай бұрын
Hi ma'am. Can a microbiology graduate opt for pharmaceutical regulatory affairs ?
@pharmacamp 5 ай бұрын
Of course they can.
@dreamoutloud4942 8 ай бұрын
Very helpful. Keep doing what you do
@pharmacamp 8 ай бұрын
Thank you:-)
@thomasmerz1843 8 ай бұрын
Promo SM
@sambhajimasal928 8 ай бұрын
Thank you Ma'am !!
@pharmacamp 8 ай бұрын
😊
@60anushkashinde99 9 ай бұрын
Mam do u have any presentation regarding EU whole regulatory process
@nileshbawane842 9 ай бұрын
Nice Neha... Informative one
@pharmacamp 9 ай бұрын
Thanks Nilesh
@arpitjaiswal272 9 ай бұрын
Neha good motivation for entry level.
@pharmacamp 9 ай бұрын
Thanks Arpit
@ankurgeete1235 9 ай бұрын
Excellent and informative presentation
@pharmacamp 9 ай бұрын
Thank you 😊
@rajibmishra6795 9 ай бұрын
Please share about NCE-1 filing details.
@pharmacamp 9 ай бұрын
Hi Rajib, sure will cover this in future videos