Mail me on Yogpharma409@yahoo.com

Hii

Thanks 👍

Thanks 👍

It is deviation and cycle will be considered complete. Deviation has to be raised for root cause analysis and impact assessment likely drying of load.

@@PharmGrow thanks for your information

What is maximum length of silicone tube/ braided hose pipe in autoclave? As per FDA norms/ EN285 or other reference?

I need to check this. I will reply once i confirm

Ok. I will work on this 👍

Thanks 👍

Thank you so much 👍

Thanks 👍

Thanks 👍

Thank you 👍

Best luck dear 👍

@@PharmGrow IS THIS MUCH QUESTION IS ENOUGH FOR INTERVIEW

Clearing interview depends on many factors. You can refer to all those guidelines in last question. That will help you 👍

Thanks 👍

Thank you 👍

The kelvin (abbreviation K), less commonly called the degree Kelvin (symbol, o K), is the Standard International ( SI ) unit of thermodynamic temperature.

Processing area is area in which batch processing is carried out like Granulation, compression, coating, formulation, filling etc. in Quarantine area we keep processed or to be processed materials like in-process area, day stock area, cold rooms etc.

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Thanks

The diagram was popularized by Kaoru Ishikawa, a Japanese quality control expert, which is why it's also commonly known as an Ishikawa diagram. So, in short, there is no difference between a Fishbone diagram and an Ishikawa diagram - they're just two different names for the same tool!

Agree.

Abosoluly yes. MSAT has growth 👍

@@PharmGrow tq sir but is it available in all pharma companies

With the title as Technology transfer department same department exist in most of companies. In recent MSAT scope has increased.

@@PharmGrow tq sir I got R&D ,AR&D and MSAT offers so which is best I don't know that's why??

We cant say any one is best. But you can evaluate based on which company has sent you offer, types of product handled etc. I will personnaly prefer RnD. From RnD you can switch anywhere and RnD itself has wide scope.

Ok

This is user specific setting. You can do it from your youtube.

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Sure. You can contact me on 9623749708. My mail ID is yogpharma409@yahoo.com

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Welcome 👍

Ideally this is joint responsibility. User department, R&D and if required vendor should perform filter validation. In most of companies set-up required for filter validation is not available with R&D,so they prefer to get it done from Vendor.

Thanks. I will work on it 👍

PHT acceptance criteria may vary based on type of equipment. No specific guideline referred for PHT acceptance criteria.

Thanks for update 👍

Yes if you claiming it sterile.

Yes. Definitely 👍

Apka contact number chahihe

Thanks for appreciation 👍

There is no as such concept of Standard cycle for autoclave. Can you please tell me what you call for, so i can answer.

There is no as such concept as standard cycle. Can you please explain for what you claim as standard cycle, so i can answer.

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Thanks

Thanks for your comment 👍

Sure. I will work on these topics

@@PharmGrow appreciated

Yes. You are right. Thanks for update.

Out of specification results.

Oos means out of specification

@@pharmapreparations Yes. You are right 👍