I think your videos are very useful for RA. If you don't mind, I would like to ask your permission to share your videos to the other website in China for the embarrassing reason that KZbin is blocked from accessing in China. Of course, I will give sources of the original website. Thank you very much!
@user-yn7kr7bv8u5 ай бұрын
I think your videos are very useful for RA. If you don't mind, I would like to ask your permission to share your videos to the other website in China for the embarrassing reason that KZbin is blocked from accessing in China. Of course, I will give sources of the original website. Thank you very much!
@6brman2246 ай бұрын
Watch MHRA board meetings. June Raine said they are now an enabling agency, revolving door with big pharma. None of you are trusted after the last 3 years, the farther you stay from me the happier I'll be. None of your made up rules apply to me.
@nakfurtulubka14 Жыл бұрын
Thank you for the informative presentation. Could you answer me, how european manufacturere handle the current situation with the proposal of the MDR. As you know there a two ways. The Notified Body should write a Confirmation letter for the manufacturer or themanufacture must write a own statement. But the Notified Bodies are currently not ready beacuse they must implement this proposal in their own process. This takes time. But if the manufacturer has no CE Certification acc. MDR and the valid MDD Certification will expired in the next time, how could manufacturer extend the registration in Saudi without the Confirmation Letter?. Accept SFDA/KSA self-written statements? Thank you.
@nusrathbaig6902 Жыл бұрын
Thank you for having an informative presentation. I would like to learn how in ghad system we can choose TFA route. Is it same as MDMA selection then which jurisdiction we have to choose if no ghtf route
@baraanofal16408 ай бұрын
In Ghad system the MDMA it is same as TFA that incudes the new regulation to include the technical file, I just say TFA to refer for the technical file documentation, MDMA: mean Marketing Authorization of Medical Devices in Saudi Arabia. So in the Ghad portal you will chose MDMA to apply for your application and completing your file.
@Abinradh Жыл бұрын
Dear Maam, Is it possible to share the presentation file here. It would be very helpfull for us.
@regdeskrims Жыл бұрын
Please provide your company email so that we can share the presentation slides with you. Thank you.
@alliebart33002 жыл бұрын
Nice video, I put on my Freestyle Libre 14days glucose sensor with NightRider! It's so good because 1) It shows if your sugars are trending up or down. 2) Give alarms if you go too low or too high. It is an amazing tool.
@alexanderwong35103 жыл бұрын
i want to register covid-19 antigen tests ,please contact me 86 18761880911
@lousheehan98253 жыл бұрын
Thank you for this. Might you also send us a compendium of the e-mail questions and answers?
@Cupcakeforever1233 жыл бұрын
Hi Priya, this was indeed a very useful webinar, however as you promised in the end of this video, kindly conduct more webinars covering Saudi FDA specially the new rules & regulations. Thanks a Lot.
@lablinkspk3 жыл бұрын
Please give me your contact number
@unamcdonagh43963 жыл бұрын
What is the name of draft guidance
@SMARTSServices3 жыл бұрын
SMARTS Services is a company which provide low cost regulatory consultancy services to get product registration from Drug Regulatory Authority of Pakistan (DRAP), Ministry of National Health Services Regulations & Coordination Islamabad, Pakistan. If you have any queries or require any further information please do not hesitate to contact us 24/7 at cell # 0333-4776655 or e-mail at [email protected] or visit www.drapregistration.com