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Pharma Regulatory Updates 2025 | FDA, EMA, EU GMP, USP, ICH, PIC/S – What Changed?
Pharmaceutical regulations are evolving faster than ever in 2025.
Global health authorities like US FDA, EMA, EU GMP, WHO, USP, ICH, PIC/S, TGA, and ISPE have introduced critical updates, finalized guidances, revised annexes, and stronger inspection expectations that every pharma professional must understand.
In this video, Pharmalytics delivers a clear, summarized, and practical overview of the most important pharma regulatory updates for 2025, based on official regulatory publications, regulatory councils, and industry journals.
This video is highly valuable for:
✔ Quality Assurance (QA)
✔ Quality Control (QC)
✔ Regulatory Affairs (RA)
✔ Validation & Compliance
✔ Manufacturing & R&D
✔ Pharma students & job seekers
🔍 What You’ll Learn in This Video: https://youtu.be/FeL8a0MIVDA
EU GMP new drafts and revised annex expectations
FDA finalized Computer Software Assurance (CSA) guidance
USP finalized & draft General Chapters
ICH focus on stability & lifecycle management
PIC/S inspection upgrades and global GMP harmonization
WHO & ISPE regulatory direction for 2025
What regulators REALLY expect from pharma professionals
TIMESTAMPS
00:30 – Why 2025 Is a Critical Year for Pharma Regulations
00:55 – EU GMP: New Drafts & Annex Updates
02:40 – FDA: Finalized CSA Guidance & Compliance Focus
04:20 – USP: Finalized & Draft General Chapters
05:50 – ICH: Stability & Lifecycle Management Focus
07:10 – PIC/S: Inspection Expectation Upgrades
08:20 – WHO & ISPE: Global Regulatory Alignment
08:50 – What Regulators Expect from Pharma Professionals in 2025
09:10 – Final Summary & Career Advice
If you want more regulatory insights, GMP updates, validation knowledge, and pharma career guidance, support Pharmalytics by:
👉 Subscribe to the channel @Pharmalytics
👉 Like the video
👉 Comment “More Regulatory Updates”
👉 Share with your pharma colleagues
Видео Pharma Regulatory Updates 2025 | FDA, EMA, EU GMP, USP, ICH, PIC/S – What Changed? канала Pharmalytics
Global health authorities like US FDA, EMA, EU GMP, WHO, USP, ICH, PIC/S, TGA, and ISPE have introduced critical updates, finalized guidances, revised annexes, and stronger inspection expectations that every pharma professional must understand.
In this video, Pharmalytics delivers a clear, summarized, and practical overview of the most important pharma regulatory updates for 2025, based on official regulatory publications, regulatory councils, and industry journals.
This video is highly valuable for:
✔ Quality Assurance (QA)
✔ Quality Control (QC)
✔ Regulatory Affairs (RA)
✔ Validation & Compliance
✔ Manufacturing & R&D
✔ Pharma students & job seekers
🔍 What You’ll Learn in This Video: https://youtu.be/FeL8a0MIVDA
EU GMP new drafts and revised annex expectations
FDA finalized Computer Software Assurance (CSA) guidance
USP finalized & draft General Chapters
ICH focus on stability & lifecycle management
PIC/S inspection upgrades and global GMP harmonization
WHO & ISPE regulatory direction for 2025
What regulators REALLY expect from pharma professionals
TIMESTAMPS
00:30 – Why 2025 Is a Critical Year for Pharma Regulations
00:55 – EU GMP: New Drafts & Annex Updates
02:40 – FDA: Finalized CSA Guidance & Compliance Focus
04:20 – USP: Finalized & Draft General Chapters
05:50 – ICH: Stability & Lifecycle Management Focus
07:10 – PIC/S: Inspection Expectation Upgrades
08:20 – WHO & ISPE: Global Regulatory Alignment
08:50 – What Regulators Expect from Pharma Professionals in 2025
09:10 – Final Summary & Career Advice
If you want more regulatory insights, GMP updates, validation knowledge, and pharma career guidance, support Pharmalytics by:
👉 Subscribe to the channel @Pharmalytics
👉 Like the video
👉 Comment “More Regulatory Updates”
👉 Share with your pharma colleagues
Видео Pharma Regulatory Updates 2025 | FDA, EMA, EU GMP, USP, ICH, PIC/S – What Changed? канала Pharmalytics
harma regulatory updates 2025 pharma regulations 2025 FDA CSA guidance EU GMP annex updates EMA GMP 2025 USP general chapter update ICH guidelines 2025 ICH stability guidelines PIC/S inspection trends WHO GMP guidelines pharmaceutical compliance GMP training pharma quality assurance regulatory affairs pharma validation in pharma data integrity GMP quality culture pharma Pharmalytics CSV QbD GMP ALCOA+ USFDA ICH EU Validation Qualification ISPE GAMP 5 AI Pharma
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29 декабря 2025 г. 5:00:06
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