This video will tell you Deviation handling in Pharmaceutical industry, Deviation management in pharma industry and will let us know that what is Deviation.
Пікірлер: 163
@rajatsharma45399 ай бұрын
Helpful
@nileshchudasama43238 ай бұрын
Nice👍
@loveforpharma9346 ай бұрын
Thanks ✌
@PriyankaPandey-vm3fc2 жыл бұрын
Sir please make a detailed vedio on calibration of weight balance ⚖️⚖️⚖️
@rahulbhutnar28022 жыл бұрын
Badhiya
@mohammedtareqaziz47102 жыл бұрын
Very informative video. Love & respect from Bangladesh
@loveforpharma9342 жыл бұрын
Mr. Tareq. thanks for watching and appriciating my video, specifically when when you said love from Bangladesh it touched my heart. Thanks a lot.
@deepakgaur55442 жыл бұрын
Bahut badhiya
@dattatraydungahu19513 жыл бұрын
Nice
@loveforpharma9343 жыл бұрын
Thanks
@Hillboy...2 жыл бұрын
Very helpful video sir, I'm working IPQA department in pharma company.
@loveforpharma9342 жыл бұрын
All the best
@user-qc8nx3zc3t2 жыл бұрын
Nice information
@gurramkondasalam13292 жыл бұрын
Dear sir, excellent job but voice in little room resound. Thank you so much you providing best information
@anumehta94624 жыл бұрын
thank you so much sir to give such good information 🤗🤗🤗🤗👏👏👏👏👏👏
@loveforpharma9344 жыл бұрын
Thanks Dear
@fury_goals59233 жыл бұрын
Ooooooooooooo99
@rajivofficial.87923 жыл бұрын
Very good🌹🌹🌹🌹🌹🌹🌹🌹🌹🌹 good information
@loveforpharma9343 жыл бұрын
Thanks dear
@aabhyasharma97523 жыл бұрын
Good information sir.
@loveforpharma9343 жыл бұрын
Thanks and welcome
@SaiSai-st9nf2 жыл бұрын
Excellent 👏 please make more videos...... We have no of topics, I want to learn in your easy way
@loveforpharma9342 жыл бұрын
Will upload soon
@AmanYadav-tc4um2 жыл бұрын
Good lecture
@shivrajwadekar9807 Жыл бұрын
Thanx sir
@dilipbaganiya51803 жыл бұрын
Good information for everyone..... Now my one sugesion Pls provide Reason for broken/damade tablets in BQS & CAM nMX machine
@loveforpharma9343 жыл бұрын
Thanks dear to like d video, sure I will make d video as demand
@shrinivaasa3 жыл бұрын
Bring more video's sir
@loveforpharma9343 жыл бұрын
sure dear
@kapilwalia274 жыл бұрын
Superb sirji thank you
@joganikrunal6519 Жыл бұрын
Thank you for this video 🎉🎉
@loveforpharma93410 ай бұрын
Ur welcome
@BharathKumar-gm5zz3 жыл бұрын
Hi sir , In Analytical R&D- Is analytical development formulation department is better for career growth in pharma.
@shwetathakur31584 жыл бұрын
Change in shipper size in secondary packing is also an example of planned deviation
@loveforpharma9343 жыл бұрын
Sorry dear any how I just skipped your question.It depends that if the change is temporary and preplanned then it would comes under planned deviation.
@rameshmanda38773 жыл бұрын
Thank u sir .most valuable information shared to us . Could Pls explain about change control , incident ..
Sure y not, but as I told earlier that due to lock down I am stocked somewhere, as soon d lockdown get withdraw, I will post my new videos.
@deepakjaiswal39883 жыл бұрын
Please make a video for change control
@loveforpharma9343 жыл бұрын
sure
@ganeshhiware25154 жыл бұрын
Superb video sir, change control ka video banayi na
@loveforpharma9344 жыл бұрын
Thanks dear for liking d video, well dheera dheera sare topic cover karne ki koshish hai, waise agar achcha laga hi to plz video ko share or channel ko subscribe zaroor kijiyega
@anilkumarthemburu37174 жыл бұрын
Very useful
@loveforpharma9344 жыл бұрын
Glad you think so!
@anilshewale96494 жыл бұрын
Godd sir
@qualityassurance46463 жыл бұрын
Good Information. I have a question: should I include an Impact Assessment section in my Deviation template?
@loveforpharma9343 жыл бұрын
ya sure y not, even it would be better to estabilish your deviation
@vikassingh-91183 жыл бұрын
Sir change control KO bhi btayiye
@loveforpharma9343 жыл бұрын
sure dear
@jayachandrank10754 жыл бұрын
Dear Sir Please explain what is the difference between Deviation and Event in pharmaceutical industry and give examples. I am confused literally between which one is deviation and which one is event. If one person did not wear his gowning in production is this event or deviation? One manufacturing step not followed is this event or deviation ?
@loveforpharma9343 жыл бұрын
well dear i already explain d same to one of my subscriber. you may read d explanation on my video for deviation's comment box.
@shashikantrao5524 жыл бұрын
Explanation very simple Sir Please explain 21cfr & urs
@loveforpharma9344 жыл бұрын
well you may watch mu video on ALCOA and i will capture urs in my next video.
@hermosadios3084 жыл бұрын
I like it
@loveforpharma9344 жыл бұрын
sorry for late reply and thanks a lot to loke d video
@pinkubisoyi19953 жыл бұрын
Well done Sir ... So easy way to Explain ... I think you have pharmaceutical Employee ?
@loveforpharma9343 жыл бұрын
Thanks dear yes I am a pharma employee
@dharmendrarautela95493 жыл бұрын
Thanks sir..
@loveforpharma9343 жыл бұрын
welcime dear
@ajaysingh-iz6mf3 жыл бұрын
Hlo sir kindly give knowledge of warehouse Department
@loveforpharma9343 жыл бұрын
any specific point or general
@deonath2ray7114 жыл бұрын
Good topics sir I like it but now a daya's peoples are saying planned and unplanned deviation are closed
@loveforpharma9344 жыл бұрын
Well dear it's right, but if you will see my video about difference between GMP and CGMP, there I explain that to execute new guidline really takes time, same is in this case it is till low not mandatory, as B grade and C grade company can't perform their activities without Deviations.
@nitishpandey50104 жыл бұрын
Veri nice sir 🙏💕 thank u so much love ❤😘❤😘u Sir aise hi aage bhi Gmp vs cgmp??? Btaaiyega??
@loveforpharma9344 жыл бұрын
Okndear thanks n ofcourse
@vikassingh28774 жыл бұрын
Dear sir , Thanx a lot for explaining nicely about deviation! I hv some doubt like if in my STP no of blank injections mentioned 2 but by mistaken I gave one shall we consider as a deviation! Second during analysis if I forgot to give entry in log book!!
@loveforpharma9344 жыл бұрын
Well dear in this case you may raise a incident because now you cab not rectify you mistake in same sequence , you need to repeat he sequence that's why you need to raise an incident.
@vikassingh28774 жыл бұрын
@@loveforpharma934 thanx a lot sir!
@vijaykusalkar3285 Жыл бұрын
Sir deviation ke liye investigation kar na ho to kon kon se document collect kar hoga
@loveforpharma93410 ай бұрын
Deviation k liye us particular deviation se related har important docs collect karne honge matlab jo kuch b us deviation se associated hai
@abhisheknandy22614 жыл бұрын
Explain about Equipment periodic qualifications necessaries?
@loveforpharma9344 жыл бұрын
Will capture in my another video
@VishalPatel-ms2vr4 жыл бұрын
Sir please discribe different b/w incident and unplanned deviation
@loveforpharma9344 жыл бұрын
Dear incident is an unrecoverable accident which happen unintentionally, while an Unplanned Deviation is an activity which we may do intentially and the same could be recoverable
@m.skumar1473 жыл бұрын
@@loveforpharma934 please make a clear video on this sir
@vikassingh-91183 жыл бұрын
Gmp and CGmp bhi btayiye please
@loveforpharma9343 жыл бұрын
kzfaq.info/get/bejne/Y8pyatWirq-amZc.html is the link for my video about difference between GMP N cGMP
@sunteljet90424 жыл бұрын
Sir how we can close planned deviation, this also required change control to be close with deviation?
@loveforpharma9344 жыл бұрын
If there is any permanent change which is caused by that particular deviation then only u need to take change control, other wise you close the same by prescribed format.
@sunteljet90424 жыл бұрын
@@loveforpharma934 ok thanks sir
@Kalpana03114 жыл бұрын
Thanku sir nice video aap sir change control and qms ke baare me discuss kijiye
@loveforpharma9344 жыл бұрын
Definitely dear, these days I am quite busy with some of my personal issues, but very soon I will share videos on said topics. THANKS FOR LICKING D VIDEO. PLEASE SHARE THE VIDEOS WITH YOUR KNOWN ONES.
@lokeshtijare4594 жыл бұрын
The presentation is very good but what about the impact assessment ........need to addreesed during handling of deviation....
@loveforpharma9344 жыл бұрын
Thanks dear for liking the video, obviously impact assessment is a part of Deviation but it is itself a complete and big topic, so will surely capture under my another video.
@shwetathakur31584 жыл бұрын
Sir plz make vedio on three types of stability chambers used in quality assurance pharma ( long term , short term or intermediate term stability chamber and accelerated term stability chamber )
@loveforpharma9344 жыл бұрын
Ok dear ofcourse
@shwetathakur31584 жыл бұрын
@@loveforpharma934 Thanks a lot sir
@shwetathakur31584 жыл бұрын
@@loveforpharma934 sir plz also explain on what basis medicines or products are placed in different chambers ?
@RV-jy3jv2 жыл бұрын
Walk the Talk
@sunteljet90424 жыл бұрын
Sir i is there any event/source except deviation that lead to capa ??
@loveforpharma9344 жыл бұрын
CAPA is taken for any incident, market complain or any other activity which leads failure and its investigation.
@sunteljet90424 жыл бұрын
@@loveforpharma934 thank you sir
@haribasyal22344 жыл бұрын
sir can u plz upload a video about IQ,OQ and PQ document sample with example
@loveforpharma9344 жыл бұрын
Dear I think u didnt subscribe my channel otherwise you must know abt my latest video, which is for IQ, OQ, PQ, DQ and other qualification parts. Just go to my channel and watch d video
@haribasyal22344 жыл бұрын
I went through those but those have only explainations about what IQ,OQ and PQ is not the whole document sample....
@loveforpharma9344 жыл бұрын
@@haribasyal2234 well dear whole documents can't share sorry
@loveforpharma9344 жыл бұрын
@@haribasyal2234 but I will try to share d samples, ok
@haribasyal22344 жыл бұрын
@@loveforpharma934 thank you sir
@vikassingh-91183 жыл бұрын
Sir app age ki video kyu nhi bna rhe please change control pr bnayiye
@loveforpharma9343 жыл бұрын
well dear agar aapne gaur kiya ho to mai just kisi guidline ko padta nahi hu balkj use is tarah se narrate karne ki koshish karta hu ki wo easly kisi ko b samajh aa jaye ir aisa karne k liye muze kafi time dena padta hai. filhal mai apne kisi or project me busy hu or isis liye video nahi bana pa ra hu but jaldi hi banaunga aap logo k liye.THANKS
@vishugoo3 жыл бұрын
Please make video on change control and other QMS
@shwetathakur31584 жыл бұрын
Sir mixing of 2 different batches ye kiske under aayega ...major deviation ya phr critical deviation ke under ??
@loveforpharma9344 жыл бұрын
Dear it will come under incident
@anilwaybhase23203 жыл бұрын
Critical
@shwetathakur31584 жыл бұрын
Sir can you please explain the difference between unplanned deviations and Non conformity report
@loveforpharma9344 жыл бұрын
NCRs are the activities performed intentionally or unintentionally by some persons, which were not as per your standard procedures.
@shwetathakur31584 жыл бұрын
@@loveforpharma934 machine ki speed agar limit se bahar ho production fast krne ke liye to ye NCR ke under aayega ya unplanned deviation ... As per Ur definition NCR ke under because ye ek person kr rha hai ?
@loveforpharma9344 жыл бұрын
Dear m/c ki limit always m/c QUALIFICATION or product validation k samay verify kar li jati hai jaise minimum medium or maximum, yani ki m/c ki maximum limit par hum apne product ko chala k pahle hi validate kar chuke hote hain, is liye machine ki speed limit badhana Deviation nahi hota until unless it should mentioned in your BMR or BPR
@loveforpharma9344 жыл бұрын
And as I said ki wo activities which seems like accident may come under incident and also which were near to recover, machine ki speed kabi b accidentally nahi badri hai hamesh intentionally badaya jati hai or use ham jab chahe change ya manage kar sakte hain
@shwetathakur31584 жыл бұрын
@@loveforpharma934 ok sir thnku 100 Percent satisfied with Ur answer 👍
@ChandanSingh-gd3gy4 жыл бұрын
Media filling ke bare me batao
@loveforpharma9344 жыл бұрын
Well dear sure but abhi kuch or videos pipeline me hai, so after those videos
@hermosadios3084 жыл бұрын
But apne ye nhi btaya ki kitne din mai ise close krte hai aur agr utne bhi nhi ho paya close fir kya karte hai??????
@loveforpharma9344 жыл бұрын
Of course dear, every activity should complete within a time frame and the same should mention in your respective SOP, any deviation in said time line should cover under Unplanned deviation.
@dharmapresents85003 жыл бұрын
Slide is not visible
@loveforpharma9343 жыл бұрын
Not visible means, will u please tell me, coz no body complain me till, d video is already have thousand of views
@navashbasha88693 жыл бұрын
Thanks you so much
@unpluggedartist24664 жыл бұрын
Plz tell me difference between non compliance n Incident......
@loveforpharma9344 жыл бұрын
well dear, non compliance is when you dony obey the SOPs, protocol or other written procedures. It may intentional or unintentional. on the other hand incidence is an uncontrolled event or accident which probably take palce un intentionally.
@unpluggedartist24664 жыл бұрын
@@loveforpharma934 but if we don't follow the written procedure it is called deviation.......
@loveforpharma9344 жыл бұрын
@@unpluggedartist2466 yes dear there is again difference between incident and Deviation.
@unpluggedartist24664 жыл бұрын
@@loveforpharma934 Dear sir I just want to know difference between non conformance n incident.....
@loveforpharma9344 жыл бұрын
@@unpluggedartist2466 dear when we do not follow d written procedures it would definitely a Deviation. The chalan what we raised to address that Deviation or such things is known as NCR or non conformance report.
@vikashjurel89534 жыл бұрын
Kindly tell me the Tcd of deviation
@loveforpharma9344 жыл бұрын
Good question dear, actually the exact TCD is not mentioned in any of guidline but it depends on the type of Deviation generated. We shall categories the TCDs for Deviation in justified way in our SOP.
@anumehta94624 жыл бұрын
Good morning sir
@loveforpharma9344 жыл бұрын
Gud morning dear
@Shorts-mk2zc4 жыл бұрын
Hii
@dmadityakhorne68274 жыл бұрын
Hi
@nitishpandey50104 жыл бұрын
Sir ye kahe rhe h ki data integrity?? And alcoa bhi batayega??
@loveforpharma9344 жыл бұрын
Of course dear as I said one by one I will try to cover every technical and non technical point, but obviously it will take time. To prepare a single video it take lot of efforts and time so keep patience and weight.
@nitishpandey50104 жыл бұрын
Ok thanks hm wait krenge?
@ManjuDevi-ik5mz3 жыл бұрын
Procesor to btaya ni
@loveforpharma9343 жыл бұрын
????
@Itsraaz-wl6jd4 жыл бұрын
Deviation hota kya h...iska matlab h kya...🤔🤔🤔
@loveforpharma9343 жыл бұрын
well dear you may go through my video for deviation kzfaq.info/get/bejne/eciloJmLv6e3l4U.html, this is d link.
@shwetathakur31584 жыл бұрын
Amber bottle breaking during filling ..ye incident ke under aayega ya phr unplanned deviations ??
@loveforpharma9344 жыл бұрын
Definitely it's a incident, actually incident ko moti tarah se samajhna chaho to jo activities accident ki tarah ho or jo almost non recoverable ho wo hamesha incidence me aati hain, jaise koi spillage.
@shwetathakur31584 жыл бұрын
@@loveforpharma934 Thanku so much sir
@loveforpharma9344 жыл бұрын
Wais bahot sare log Unplanned Deviation ko hi incident me cover karte hain, but it's a point of common sense ki ek hi cheez ke liye do terminology kyo hogi kya kisi or cheez ki do terminology hai pharma me????
@shwetathakur31584 жыл бұрын
@@loveforpharma934 yes u r right sir Sir agar koi person without gowning enter krta hai area me to ye unplanned deviation ke Ander aayega . Bt as per Ur definition of NCR ye Non conformity report ke under bhi aa skta hai ??
@shwetathakur31584 жыл бұрын
Mera jo doubt that unplanned deviation or incident ka vo to 100 percent clear kr diya Apne bt I m still confused between unplanned deviation and NCR