Cleaning Validation | CEHT | DEHT
5:26
Sterilization Science
3:37
6 ай бұрын
Пікірлер
@CarlosPerez-ob1tx
@CarlosPerez-ob1tx 20 күн бұрын
UN EXCREMENTO COMO MADURO SOLO APESTA A VENEZUELA Y A TODA AMERICA
@vipulbhatu
@vipulbhatu 23 күн бұрын
From where can we purchase a validation kit can you suggest
@PharmaGyan
@PharmaGyan 23 күн бұрын
Okay i will look into it and suggest a good vendor
@vishakhagour3365
@vishakhagour3365 25 күн бұрын
Thanks
@deepufitness12ww
@deepufitness12ww 27 күн бұрын
Thanks sir ❤
@pravinsingh8170
@pravinsingh8170 28 күн бұрын
Sir Em m kya revised huya grade a me
@PharmaGyan
@PharmaGyan 28 күн бұрын
Limits of 0.5 and 5 micron particles revised, also clarification on viable particles monitoring limits provided, much more changes for detailed information please watch our upcoming videos and you can also read EU GMP Annexure 1, 2022
@vaibhav6046
@vaibhav6046 Ай бұрын
Why we cant measure 1,2,3,4 micron particles??
@PharmaGyan
@PharmaGyan Ай бұрын
Absolutely we can measure all particle size but in Pharmaceutical Industries we only measure recommended particle size as per respective guidelines like EU GMP Annex 1, ISO 14644
@PankuThakur-nv2mk
@PankuThakur-nv2mk Ай бұрын
Sir dealy before hold vlt me kis bjha se aata rejoin tell me please
@PharmaGyan
@PharmaGyan 28 күн бұрын
Sorry I dont understand your query
@user-vx6kp4dt7f
@user-vx6kp4dt7f Ай бұрын
Cooling water kha used hota h
@PharmaGyan
@PharmaGyan Ай бұрын
For cooling of load items
@krish_krish354
@krish_krish354 Ай бұрын
What is the difference between method validation and process validation
@PharmaGyan
@PharmaGyan 28 күн бұрын
Method validation is generally used in QC to develop testing methodology such as testing methods for particular products Process validation is generally used to validate processes such as Manufacturing process etc
@krish_krish354
@krish_krish354 27 күн бұрын
Thank you sir
@mangeshmochi460
@mangeshmochi460 Ай бұрын
Thanks sir best video
@PharmaGyan
@PharmaGyan Ай бұрын
Most welcome
@vinodsahni8179
@vinodsahni8179 Ай бұрын
Nice 👍
@PharmaGyan
@PharmaGyan 24 күн бұрын
Thanks ✌
@carryminati3144
@carryminati3144 2 ай бұрын
Sir data integrity pai bhi video bnaiye
@PharmaGyan
@PharmaGyan Ай бұрын
Okay
@senapathidileepkumar532
@senapathidileepkumar532 2 ай бұрын
Can u please tell me in vacuum leak test which pressure we need to consider either positive or negative and why?
@PharmaGyan
@PharmaGyan 2 ай бұрын
If your chambers pressure is more than atmospheric pressure then it is considered as positive pressure but if your chamber pressure is less than the atmospheric pressure then it is considered as negative pressure. Don't correlate it with - & +.
@MZM49
@MZM49 2 ай бұрын
Sir,very informative ,thanks
@sourabhshetake0909
@sourabhshetake0909 3 ай бұрын
👍 nice information
@PharmaGyan
@PharmaGyan 2 ай бұрын
Thanks
@TinkuKumar-uv3yh
@TinkuKumar-uv3yh 3 ай бұрын
हिंदी में नही।हैं
@brijmohantiwari2011
@brijmohantiwari2011 3 ай бұрын
Wow, super information of IPR
@PharmaGyan
@PharmaGyan 2 ай бұрын
Thank you
@ramukrishnudu6526
@ramukrishnudu6526 3 ай бұрын
Very important topics discussed..
@yogeshkoli851
@yogeshkoli851 3 ай бұрын
Autoclave criteria kya he sir...?
@PharmaGyan
@PharmaGyan 3 ай бұрын
A video will be published very soon for Autoclave Qualification Acceptance Criteria
@yogeshkoli851
@yogeshkoli851 3 ай бұрын
Link send kro n sir
@51vetrivels8
@51vetrivels8 3 ай бұрын
This is process validation type..Not a validation type..This is wrong answer of type of validation
@51vetrivels8
@51vetrivels8 3 ай бұрын
Validation type 1) analytical method validation 2) process validation 3) equipment qualification 4)vander qualification..etc..
@PharmaGyan
@PharmaGyan 2 ай бұрын
Don't mess up, i am explaining few parts not a complete guide here. Thank you for your queries.
@VikramJadhav-tp5li
@VikramJadhav-tp5li 3 ай бұрын
Very nice information...
@Virqlloveindia
@Virqlloveindia 3 ай бұрын
Goood
@RuthiJaanvi
@RuthiJaanvi 3 ай бұрын
Why using single slot and double slot stopers .
@PharmaGyan
@PharmaGyan 3 ай бұрын
Regardless the number of vents, during the lyophilization process, after the freezing step, the ice crystals sublimate via the vent(s) in the rubber stopper. It has been observed that the rate of moisture transfer from the vial increases as the cros-sectional area of the vent increase itself.
@Sylvie_in_the_Sea
@Sylvie_in_the_Sea 3 ай бұрын
I am sad it is not in English 😢
@RakeshKumar-sx8zm
@RakeshKumar-sx8zm 4 ай бұрын
Useful calculation..... thanks for sharing
@mrbappy3474
@mrbappy3474 4 ай бұрын
Nice presentation
@PharmaGyan
@PharmaGyan 4 ай бұрын
Glad you liked it
@socialseller347
@socialseller347 4 ай бұрын
बहुत अच्छा लगा आपका ये वीडियो ओर भी सम्पूर्ण जानकारी इसी तरह हिन्दी व इंग्लिश दोनों में समझाते रहना जय श्री राम 🚩
@PharmaGyan
@PharmaGyan 4 ай бұрын
Dhanyabad Jai Shree Ram
@PraveenS-lv2gh
@PraveenS-lv2gh 4 ай бұрын
Why only 3520 and 20?
@PharmaGyan
@PharmaGyan 4 ай бұрын
Its given in EU GMP Annexure 1
@PraveenS-lv2gh
@PraveenS-lv2gh 4 ай бұрын
Hi sir I have one doubt. Why NVPC limit is 20 and 3520 only?
@PharmaGyan
@PharmaGyan 4 ай бұрын
Its Given in EU GMP Annexure 1
@parvinder_singh_69
@parvinder_singh_69 4 ай бұрын
is negative pressure possible in autoclave?
@PharmaGyan
@PharmaGyan 4 ай бұрын
So what is vacuum?
@awineshtripathitripathi7016
@awineshtripathitripathi7016 4 ай бұрын
How to write CQP
@PharmaGyan
@PharmaGyan 2 ай бұрын
its not about writing CQP you need to identify first all relavent CQPs related to your process based on impact on the product quality and SISPQ, then write the same for CQP.
@drx.trimbak3126
@drx.trimbak3126 5 ай бұрын
Very Informative Information Thanks Sir
@PharmaGyan
@PharmaGyan 4 ай бұрын
Thanks for liking
@Gulfraj_kinda
@Gulfraj_kinda 5 ай бұрын
Sir exam mai ayga ky
@PharmaGyan
@PharmaGyan 2 ай бұрын
May be
@nileshbhusari5559
@nileshbhusari5559 5 ай бұрын
Why NVPC carried out for 3 days??
@PharmaGyan
@PharmaGyan 2 ай бұрын
Watch this video, you will get more clarity on this. kzfaq.info/get/bejne/pdt8iK-D2LqmnGg.html
@hiralpatel1160
@hiralpatel1160 5 ай бұрын
How can we decide in which ISO class our clean room should include? We don't know particle count of room.
@PharmaGyan
@PharmaGyan 5 ай бұрын
For that you need to do qualification of that room and based on the outcome of the result you can classify that room
@ramanpurohit7922
@ramanpurohit7922 5 ай бұрын
Sir 3day k liye kyu karte h
@user-gr6sj6lr3n
@user-gr6sj6lr3n 6 ай бұрын
Very knowledgeable videos
@akyadav7742
@akyadav7742 6 ай бұрын
How long it take from the date of order is placed for manufacturing the capsule
@ranjeetnagarkoti3274
@ranjeetnagarkoti3274 6 ай бұрын
Very helpful.thank you.
@anantbadode7193
@anantbadode7193 6 ай бұрын
Can you explain about Air detection test
@PharmaGyan
@PharmaGyan 6 ай бұрын
Sure we will prepare a video on that
@anjigoud6697
@anjigoud6697 6 ай бұрын
Good information sir.
@adnanazhar7227
@adnanazhar7227 7 ай бұрын
Sir am not found chapter 4
@adnanazhar7227
@adnanazhar7227 7 ай бұрын
Thanks
@adnanazhar7227
@adnanazhar7227 7 ай бұрын
Sir where is chapter 4
@adnanazhar7227
@adnanazhar7227 7 ай бұрын
Sir where is chapter 4
@adnanazhar7227
@adnanazhar7227 7 ай бұрын
👍👍👍👍👍
@adnanazhar7227
@adnanazhar7227 7 ай бұрын
Very informative
@PharmaGyan
@PharmaGyan 2 ай бұрын
Glad it was helpful!
@adnanazhar7227
@adnanazhar7227 7 ай бұрын
❤❤❤❤❤
@adnanazhar7227
@adnanazhar7227 7 ай бұрын
👍👍👍👍👍