Why Change Control? | Drug Disaster se GMP & CCP ka Birth | Pharma QA

Описание: Kya aap jaante ho ki GMP aur CCP rules ka janam ek Drug Disaster ki wajah se hua?
Is video me hum us tragedy ki kahani samjhenge jisne pharma industry ko hamesha ke liye badal diya.


Is video me maine explain kiya hai:
✔ Drug disaster kya tha
✔ Patients par uska kya impact pada
✔ Kaise regulatory bodies alert hui
✔ GMP (Good Manufacturing Practices) ka birth kaise hua
✔ CCP (Critical Control Points) concept kaise develop hua
✔ Pharma quality systems ka foundation kaise bana

Ye video Change Control series ka Video 1 hai jahan hum quality system ke roots ko samajh rahe hain, taaki aage ke advanced topics logically clear ho jaayein.

🔹 Who Should Watch?

👉 Pharma QA / CQA professionals
👉 Freshers entering pharma industry
👉 GMP, Audit & Compliance me kaam karne wale log
👉 Validation & Quality System learners

👉 Agar aap pharma quality ko sirf rules nahi balki logic ke saath samajhna chahte ho,
channel ko subscribe karein aur video ko like karein.

🔗 Video - 2 Link:
   • Change Control Explained | 3 Questions Tha...  

🔗 Video - 1 Link: Why Change Control in Pharmaceutical
   • Why Change Control? | Drug Disaster se GMP...  

Quality Risk Management Demonstration
   • Quality Risk Management (QRM) Demo | How t...  

Corrective Action & Preventive Action
   • CAPA in Pharmaceutical Industry | Correcti...  

Change Control
   • Change Control in Pharmaceuticals | Comple...  

This pharma education video explains drug disaster history, GMP history pharma, pharma quality system evolution, CCP pharma concept and change control pharma fundamentals.

#DrugDisaster
#GMP
#PharmaQuality
#ChangeControl
#PharmaQA




⚠️ DISCLAIMER: FOR EDUCATIONAL PURPOSES ONLY
This video is created solely for educational and training purposes related to pharmaceutical quality systems.
The information shared is based on general industry knowledge, guidelines, and historical understanding of pharmaceutical regulations.
This content does not constitute professional, regulatory, or legal advice and should not be considered a substitute for site-specific SOPs, QMS, or regulatory requirements.
Viewers are advised to always refer to current regulations and official guidance issued by authorities such as USFDA, MHRA, ICH, WHO, and their organization’s internal quality systems before implementation.
The creator of this channel shall not be held responsible for any professional, regulatory, or legal actions taken based on the content of this video.
Use of this information is at the viewer’s own discretion and risk.
Any copyrighted material used is for educational and research purposes under the Fair Use doctrine.
The views and opinions expressed in this video are strictly personal and do not represent the views, policies, or positions of my current or previous employers.
Technical Talk – Gopal Mandloi | Independent Professional Education