Sir please upload videos of whole industrial pharmacy I will be be very grateful to you Your teaching techniques is very impressive. Concept building classes.
Content uniformity and blend uniformity are both critical concepts in pharmaceutical manufacturing and quality control. Here's a brief explanation of the differences between them and how you can express them during an interview: Content Uniformity: Content uniformity refers to the consistency of the active ingredient's concentration within each individual dosage unit (e.g., tablet or capsule) of a pharmaceutical product. In other words, it ensures that each unit contains the specified amount of the active ingredient, which is crucial to ensure consistent therapeutic efficacy and safety for patients. Variability in content uniformity can lead to potential under-dosing or over-dosing of patients, impacting the treatment's effectiveness and safety. Blend Uniformity: Blend uniformity, on the other hand, focuses on the uniform distribution of all the ingredients, both active and inactive, within a batch of pharmaceutical material before it is further processed into dosage forms. This is especially important for solid dosage forms like tablets, where the uniformity of the mixture ensures that each tablet within a batch has a consistent distribution of the active and inactive components. Inadequate blend uniformity could result in variations in content uniformity across the finished dosage forms. During your interview, you can express your understanding of these concepts and their importance by highlighting the following points: Content Uniformity: "Content uniformity is critical to ensure that each patient receives the intended dose of the active ingredient in every dosage unit. This consistency is vital for patient safety and treatment effectiveness. Variability in content uniformity can lead to therapeutic failures or adverse effects. To achieve content uniformity, proper sampling techniques, accurate testing methods, and meticulous quality control processes are essential." Blend Uniformity: "Blend uniformity plays a pivotal role in ensuring that all the ingredients, both active and inactive, are evenly distributed within a batch of pharmaceutical material before it's further processed. This uniform distribution serves as the foundation for consistent content uniformity in the finished dosage forms. Achieving blend uniformity requires thorough mixing techniques, proper equipment, and stringent quality control measures to prevent any segregation or agglomeration that might affect the final product's quality." By articulating your understanding of these concepts and their significance, you'll demonstrate your knowledge of pharmaceutical manufacturing processes, quality control, and your commitment to ensuring product consistency and patient safety.
very nice , got a clarity on subject , thanks for sharing
Tq for all efforts to make this lecture sir...it is very helpful to us..ur down to earth.
It was very helpful sir h explained so well thank u may god bless you
Sir please upload videos of whole industrial pharmacy
I will be be very grateful to you
Your teaching techniques is very impressive.
Concept building classes.
Excellent sir 👏 thanks for give for us to watch the this video
Very well explained sir. Thanks alot.
Your way of teaching extremely good sir I learned lot about granulation an I hope it will helpful for interview ! Thanks a lot sir
Well explained
Sir please make more videos on industrial pharmacy subject😌
Sir roll compactor se hi slagging banate hai
Tysm sir
Animations are superb make more videos
Aur video banao sir..pharmaceutical guidline ke upar..
Please don't stop making videos
At least upload twice per month
Kucha malum nehi tha malum hua again thank you
Thank you Sir...
Hi dr namaz...can we make threptin like diskettes with tablet machine? Like an edible non baked biscuit
Yes. we can. juz change the punches and dies. And maintain compression force and most importantly direct compression
@@LearnwithDrNawaz thanks . Also can i use vegetable fat for granulation
@@satyenrulz yes but we have to use surfactants in particular concentration
Thank you sir good lesson
Sir interviews kese hotahee granulation mye pura questions answers ek vidio banaiye
Thanks uhhh sir..🥰🙏
Nice video
Thanku Sir and plz aap industrial pharmacy ki sabhi topics p video bnaye, that's why I need🙏🙏
Plz send me all ur topics
Thanks sir 🙏🙏
Tablet coating and liquid orals
Soft gelatin capsule or hard gelatin capsule per bhi sirr..
My question is that in wet granulation (wet screening method) why we add recipients again at the end ... If we add excipient in starting .
Lubricants will not function properly if they’re added with the with mass
Wet mass
Sir why is there soft gelatin capuseld filled with colorful granules? How are they made?
They are called as Pellets or spheroids. Prepared by extrusion and spheronization technique
@@LearnwithDrNawaz thank you so much sir for the answer. I wish you could explain that process sir next time. Thank you
Can you please explain how to caliculate froude number for rapid mixer granular.
Ya. I think choper speed divided by impeller speed
Hello Dr. Nawaz
Is the granulator agent mix with api in specific concentration ??
Or mix by experience ?
First we need to do experiment to find out what is the correct concentration. we can't adjust by experience
Sir,Make videos about important topics regarding to GPAT
Yes sir make video of gpat important topic of pharmaceutics
Nice
Sir, please explain about coating
ruclips.net/video/Jtj78WSSLVo/видео.html. Watch this
Thanks sir
Thinks sir
Sir what is the difference between content uniformity & blend uniformity & how can I express both during my interview ?
If blending is uniform, then only your content will be uniform, any changes in the blending uniformity, will also change content uniformity.
Content uniformity and blend uniformity are both critical concepts in pharmaceutical manufacturing and quality control. Here's a brief explanation of the differences between them and how you can express them during an interview:
Content Uniformity:
Content uniformity refers to the consistency of the active ingredient's concentration within each individual dosage unit (e.g., tablet or capsule) of a pharmaceutical product. In other words, it ensures that each unit contains the specified amount of the active ingredient, which is crucial to ensure consistent therapeutic efficacy and safety for patients. Variability in content uniformity can lead to potential under-dosing or over-dosing of patients, impacting the treatment's effectiveness and safety.
Blend Uniformity:
Blend uniformity, on the other hand, focuses on the uniform distribution of all the ingredients, both active and inactive, within a batch of pharmaceutical material before it is further processed into dosage forms. This is especially important for solid dosage forms like tablets, where the uniformity of the mixture ensures that each tablet within a batch has a consistent distribution of the active and inactive components. Inadequate blend uniformity could result in variations in content uniformity across the finished dosage forms.
During your interview, you can express your understanding of these concepts and their importance by highlighting the following points:
Content Uniformity:
"Content uniformity is critical to ensure that each patient receives the intended dose of the active ingredient in every dosage unit. This consistency is vital for patient safety and treatment effectiveness. Variability in content uniformity can lead to therapeutic failures or adverse effects. To achieve content uniformity, proper sampling techniques, accurate testing methods, and meticulous quality control processes are essential."
Blend Uniformity:
"Blend uniformity plays a pivotal role in ensuring that all the ingredients, both active and inactive, are evenly distributed within a batch of pharmaceutical material before it's further processed. This uniform distribution serves as the foundation for consistent content uniformity in the finished dosage forms. Achieving blend uniformity requires thorough mixing techniques, proper equipment, and stringent quality control measures to prevent any segregation or agglomeration that might affect the final product's quality."
By articulating your understanding of these concepts and their significance, you'll demonstrate your knowledge of pharmaceutical manufacturing processes, quality control, and your commitment to ensuring product consistency and patient safety.
What about crystalline powder sir..
thank you sir
Thanks. Subscribe and share with ur friends
Sir,Please make videos on Opthalmics
Sure
Hindi me boliye to jyada maja aayega
한국말로 좀 해주세요 감사합니다
sir, when to choose wet granulation?
When ur drug is 1. Not thermoliabe 2. Not undergoing hydrolysis .
@@LearnwithDrNawaz thank u so much sir
Sir what thermolibale
Heat sensitive
@@LearnwithDrNawaz thanks ji
Sir meaning batadiyega words ka I am d pharma student you teaching way is very easy.
sir aapka number milega kya
Unable confused indian
Thank you for suggestions