this was very informative and valuable the problem is the recroding of the sound was horrible
@23Change4 ай бұрын
Excellent webinar ✅
@glockeinteractive4 ай бұрын
how can I get a free copy of the power point?
@zul.cenaheyn5 ай бұрын
Is 510k documents needed for ultrasonic dental tartar removal machine?
@slz11194 ай бұрын
I think you should check 21 CFR to identify if it is class I or class 2 , most class 1 is 510k exempt.
@carol_hyejinkim10 ай бұрын
Great webinar. Thank you😊
@yumingzhao557711 ай бұрын
True expert
@DerekEdington-t4p Жыл бұрын
Thanks for the information
@Anon-up3be Жыл бұрын
This place is an email spam factory.
@timglover4180 Жыл бұрын
Really good video content and really helpful! Unfortunately I had to listen to it multiple times and keep rewinding as the sound was quite muffled, I tried it on multiple devices.
@benlee3545 Жыл бұрын
hi, your video is good. you also share some of the experience you have in software but it will be better if you can include examples of the device master record for clearer illustrations and templates etc.
@ysshaikali1643 Жыл бұрын
Thank you for your information. I learned, understand well
@jerrylee2698 Жыл бұрын
arrest the medical mafia
@lissaoneill8008 Жыл бұрын
44:50 Stock Recovery. Interested to know would this be considered stock recovery?: manufactured lot has known defect. Some part of lot was distributed but it is known that all distributed devices were used up with no harm. The firm still decides to destroy what's left in stock - would this be a stock recovery since it is known nothing is currently in distribution or it is no longer stock recovery since part of lot had been distributed and it doesn't matter whether there is nothing in distribution anymore?
@SamHarmony2 Жыл бұрын
Thank you for the content. Very helpful! Is it possible to receive a copy of this powerpoint presentation?
@AbbyGhignone-yy7yt Жыл бұрын
I miss you papa. I love you. You’re amazing.
@beaudyorcel4987 Жыл бұрын
This is a great presentation
@sonandpets1215 Жыл бұрын
What an incredibly, clear, and to the point presentation
@NazrulIslam-kb2tt Жыл бұрын
How can i get pdf of this presentation?
@liorx102 жыл бұрын
Thanks I really appreciate your explanation, it was definitely very clear and educated.
@CityWalkSHA2 жыл бұрын
Still a very good training material today! Thank you!
@davidmuseau14062 жыл бұрын
Seriously get rid of that straw Dan
@tinthings3142 жыл бұрын
Very good overview of validation principles, thank you very much
@dorrinasefi94002 жыл бұрын
I wish i read the comment. No content here!
@SanthoshKumar-np8pr2 жыл бұрын
Great session
@fadumaali57382 жыл бұрын
Thank you, I learned a lot from this webinar
@davidfrancis12992 жыл бұрын
Fantastic overview! I am saving for reference. Please let me know if there is an updated version. Great job!
@kkwok92 жыл бұрын
Nice job Thorough, formal, technical and to the point. Thank you Sir
@gxpmatters57052 жыл бұрын
kzbin.info/door/yB3GFq6cWuAZzGWpnTX70A
@daltonymd83912 жыл бұрын
sterilization is definitely design output, biocompatibility aswell
@sanketmane71092 жыл бұрын
Thank you🙂
@kkwok92 жыл бұрын
A nice presentation. This gal knows her stuff. Thank you
@abhilovemarvel18102 жыл бұрын
sir i want some book suggestion where i get knoledge abou this think
@kkwok92 жыл бұрын
This gal knows her stuff. I have heard her other presentations on your channel. Melinda is an amazing speaker
@bobtan93212 жыл бұрын
Sounds impressive but don't be taken in. NOt listed is Preventing doctors from seeing Clinical Trial Data. As it is clear, many of you are not aware of Pfizer's clinical trial data being locked up for 75 years by our boys at the FDA. Also not listed is the dictatorial ruling by the FDA to ignore the warning of the Advisory Committee on Vaccines, "Members of the FDA advisory committee struck a skeptical tone during the meeting Friday, questioning Pfizer's conclusions that immunity is waning to the point that vaccinated people of all ages" It is sad that so many people that should know better are duped by an FDA that's been running amuck. Houston, we've got a problem, a huge problem of integrity. And we are all being played.
@shivakumar-ll6ro2 жыл бұрын
Sir can you please explain me in standard iso 2859 or is 2500 Based on lot size and sample size we have accept and reject numbers I want to know how those accept and reject numbers are calculated and created .... please do needful 🙏🙏🙏
@TeW33zy3 жыл бұрын
Didn't even understand half the words? What is the document he said download. I couldn't make out the word cusid?
@TeW33zy3 жыл бұрын
What is cusid?
@jlak8922 жыл бұрын
It's QSIT- Quality System Inspection Technique. Google for examples.
@paragkale54593 жыл бұрын
nice
@kkwok93 жыл бұрын
Very nice. Information was much appreciated
@kkwok93 жыл бұрын
Good information. Thank you
@jennifercamison38153 жыл бұрын
Very helpful video
@kkwok93 жыл бұрын
Excellent presentation Thank you folks
@parveshthakur29793 жыл бұрын
Can i Get this course certification
@nguyentung54063 жыл бұрын
can you upload slide show pdf, it'll be fantasic
@BharathKumar-gm5zz3 жыл бұрын
Very good information sir, Is analytical development formulation department is come under A R&D in pharma industries.
@tlm77903 жыл бұрын
Outstanding job Dan!
@kkwok93 жыл бұрын
Good stuff Shes good at presenting
@orisolesolutions38673 жыл бұрын
Introduction to regulatory affairs. Scope and Opportunities of Regulatory Affairs . kzbin.info/www/bejne/faS1gH6Odrlsaa8
@kevinkane64183 жыл бұрын
What a complex protol(s) to follow!!!!! excellent information and clinically sound, thank you!!!!!