■ Appendix 2: Validation of water systems for pharmaceutical use. In: WHO Expert Committee on Specifications for Pharmaceutical Preparations, fortieth report. Geneva: World Health Organization; 2006: Annex 4 (WHO Technical Report Series, No. 937; www.who.int/medicines/areas/ quality_safety/quality_assurance/SupplementaryGMPValidationTRS937 Annex4.pdf?ua=1). For details on the validation of water systems for pharmaceutical use, please see: ■ WHO good manufacturing practices: water for pharmaceutical use. In: WHO Expert Committee on Specifications for Pharmaceutical Preparations, forty-sixth report. Geneva: World Health Organization; 2012: Annex 2 (WHO Technical Report Series, No. 970; Geneva, World Health Organization 2012 (WHO Technical Report Series, No. 970; apps. who.int/medicinedocs/documents/s19464en/s19464en.pdf).
Bhut aacha bhai
Osm bro 👏👏👏
Good Job 👍
Excellent 👏👏👏👏👏
Good one sir !! Keep it up 👍🏻
Well done sir👏👏👏👏Please make one video about types of water used in pharmaceutical industries.
very nice video
Brilliant.
Thanks dear , keep supporting ❤️
Very well explained sir ..
Thanks for the compliment
Nice explain sir...... please provide the all Guidelines for water system validation
Sure, I am adding these guidelines link below this video description . So go through it.
Which guideline we use for water validation?
Is which bases how we design phase III schedule
guidelines I have mentioned in the description box. You can check it out.
Very nice❤❤
Many many thanks
Vo time company manufacture tablet ya syrup nhi kr payegii aesaaaq
Phase 1 k time manufacturing completely bnd rhegi
sir kon kon se test km kr dete hai. phase 3 study me on basis of phase 1& 2
You don't need to perform tests at each stage, only routine tests need to be performed.
Nice u explaination sir ,Need sampling points protocols sir
Thanks 🙏 Sure I will share these sampling protocols soon.
Which Guidelines follow for PWS plz. Btao
■ Appendix 2: Validation of water systems for pharmaceutical use. In: WHO
Expert Committee on Specifications for Pharmaceutical Preparations,
fortieth report. Geneva: World Health Organization; 2006: Annex 4 (WHO
Technical Report Series, No. 937; www.who.int/medicines/areas/
quality_safety/quality_assurance/SupplementaryGMPValidationTRS937
Annex4.pdf?ua=1).
For details on the validation of water systems for pharmaceutical use, please see:
■ WHO good manufacturing practices: water for pharmaceutical use.
In: WHO Expert Committee on Specifications for Pharmaceutical
Preparations, forty-sixth report. Geneva: World Health Organization; 2012:
Annex 2 (WHO Technical Report Series, No. 970; Geneva, World Health
Organization 2012 (WHO Technical Report Series, No. 970; apps.
who.int/medicinedocs/documents/s19464en/s19464en.pdf).
@@PharmaScholars thanku sir
Hlo sir mke a complete video on water system source to psg end plz including guide lines....
Nice
Thanks
Mera phase 3 complete ho gya hai.
Uske baad hme kya krna cahiye.?
Uske bad hr saal continues process verification chalta he
Qualification of hplc???
I will make video in this topic soon.
Sir konse guideline Kay mutabik hum water testing kurray hain
guidelines I have mentioned in the description box. You can check it out.