it is a blessing for me that u gave me training of a week. At baddi university. It was the best experience of learning i wish i could have these sessions from Starting of our pharmacy studies Anyways that one week was very awesome.. the best lectures i ever had.. And most interesting study as well
Appreciated that you understood the basic requirements for Pharmacy students to bridge the gap between Academics and Industry requirements. We will provide training through my youtube channel continuously.
Excellent insight about the importance and correct way of preparing SOP. If these steps are followed while designing QMS system, organisations will gain competitive advantage.
Hi sir and all viewers, I have a query related to SOP reversion. As per regulatory or global standard, if there is no new update required for existing SOP version, do you still need to create a new version (during time of reversion) with the same information and mentioning about no changes done in SOP change history (or) we need not to create a new version and wait for new cycle. Many thanks in advance. Regards, Samir Das
Dear Samir, Thank you for your query. First of all we must understand the basic need for periodic revision of any GMP document. This is obvious that over a period of time, we simplify our procedures by addition or modification of contents for ease of understanding, to meet customer requirement, to meet regulatory expectations, to meet in-house improvement initiatives etc. This is unlikely that same procedure followed for decades without any improvements. Please note that if we follow our SOP on daily basis then there must be improvement suggestions over a period of time and this is nothing but periodic revision. However if we have any such procedure which is so perfect that no need any change over decades then you have to justify and keep it as such. Same shall be part of SOP on SOP document. Feel free to send me any further query on my mail id firmamentum.consultant@gmail.com
@@SunilSingh-wg9sh Does it applicable for all the Documents related to Validation ? like the Protocols(process, cleaning, equipment) and MFRs, and Documentation related to Quality ?
Good content sir
Thank you very much for your efforts in making of these valuable vdo guidance...
Thank you.
Great work for pharma industries, it's also very much helpful for students.
Exactly ! This is the basic purpose of my channel. Keep watching.
Great explanation 👌 Sir
Content well organized and conveyed clearly.
Thank you. Can we collaborate for business opportunity?
@@SunilSingh-wg9sh I am interested to know specifically what you have in mind. Also the link to your Linkedin profile is broken.
it is a blessing for me that u gave me training of a week. At baddi university. It was the best experience of learning i wish i could have these sessions from Starting of our pharmacy studies Anyways that one week was very awesome.. the best lectures i ever had.. And most interesting study as well
Appreciated that you understood the basic requirements for Pharmacy students to bridge the gap between Academics and Industry requirements. We will provide training through my youtube channel continuously.
@@FirmamentumTraining thank you so much sir..
Excellent Video, Very useful spent 21 minutes.
Thanks Mahboob for appreciations and getting useful informations.
great information ,it is useful , thank you
Excellent insight about the importance and correct way of preparing SOP. If these steps are followed while designing QMS system, organisations will gain competitive advantage.
Excellent Sir...
Great job sir
Great Sir
Thank you Gyanendra.
Good content
Can we do subsequent review of sop if there is no change found in the respective sop
Plz suggest how to do material storage bin activities??
Dear Sunil Sir,
Could you please guide me how to implement corporate procedure
sir please prepared the vdo about master formulation record , APQR
Sir make a video on handling of deviations , incident.i need to understand properly.
Sir b. Pharma Fresher ko IPQA department main jane ke liye videos bna dijiye.।।
Waiting for next video..
We are coming with our next video soon!
Hi sir and all viewers,
I have a query related to SOP reversion. As per regulatory or global standard, if there is no new update required for existing SOP version, do you still need to create a new version (during time of reversion) with the same information and mentioning about no changes done in SOP change history (or) we need not to create a new version and wait for new cycle.
Many thanks in advance.
Regards,
Samir Das
Dear Samir,
Thank you for your query.
First of all we must understand the basic need for periodic revision of any GMP document. This is obvious that over a period of time, we simplify our procedures by addition or modification of contents for ease of understanding, to meet customer requirement, to meet regulatory expectations, to meet in-house improvement initiatives etc. This is unlikely that same procedure followed for decades without any improvements. Please note that if we follow our SOP on daily basis then there must be improvement suggestions over a period of time and this is nothing but periodic revision. However if we have any such procedure which is so perfect that no need any change over decades then you have to justify and keep it as such. Same shall be part of SOP on SOP document.
Feel free to send me any further query on my mail id firmamentum.consultant@gmail.com
@@FirmamentumTraining thanks a lot sir for your response.
21CFR PART 211 means and where it's include ?
This is the regulations in US for Pharmaceutical manufacturing
Sir please help for writing statement of purpose
My qualification MSC CHEMISTRY
Choose programme pharmaceutical sciences
which guideline we need to follow for sop preparation
There is no guideline for SOP preparation. Guideline says you have to have written procedure and followed.
@@SunilSingh-wg9sh Does it applicable for all the Documents related to Validation ? like the Protocols(process, cleaning, equipment) and MFRs, and Documentation related to Quality ?
Sir opthalmic preparation ipqa m future kasa rahega
It will be good.
Sir please provide training on process validation as per USFDA and WHO also.
Sure.
Thank you.
Sir can you please make vedio on planned and unplanned deviations
Sure.
Major vs miner
Sir pharmaceutical companies me kaise apply kare....
Based on your qualification and experience, you can apply through job portal or direct to the pharma companies through web site.
@@FirmamentumTraining sir kiya aap mujhe ek link de sakte Hain....
@@rupjyotibhuyan7573 May I know whether you are experience or fresher?
@@FirmamentumTraining sir I am a fresher. I have complete my graduation in Bsc chemistry.
Sir aap pharma industry pe Kam krte hain..
No do sir tumhara plz