Pharmalytics
Welcome to Pharmalytics, your go-to YouTube channel for expert insights and practical knowledge on the pharmaceutical industry. Here, we dive deep into topics such as cGMP (current Good Manufacturing Practices), Quality Compliance, Data Integrity, and Regulatory Requirements, empowering professionals in the pharma sector to stay ahead of industry standards and best practices.
Whether you're involved in pharmaceutical manufacturing, regulatory affairs, or quality assurance, Pharmalytics offers valuable content to help you navigate complex regulations, ensure product quality, and maintain compliance. Subscribe for expert tips, industry updates, case studies, and practical guidance to enhance your understanding and success in the pharmaceutical world. Stay informed and compliant with @Pharmalytics!
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Валидация очистки в 10 этапов в фармацевтике | Полное руководство по валидации очистки
Культура качества: основа целостности данных | Мышление GMP, соответствие требованиям FDA и готов...
Личная честность в фармацевтике: скрытый двигатель культуры качества и целостности данных
CAPA в фармацевтике: внедрение, анализ первопричин и эффективность | Руководство по подготовке к ...
Передовой опыт уничтожения документов GxP | Соответствие фармацевтическим нормам и целостность да...
Pharma 4.0 Revolution: How AI & Automation Are Transforming Drug Manufacturing
Validation vs Qualification in Pharma | GMP, FDA, WHO Guidelines Explained
Qualification in Pharma Explained | Validation Life Cycle Explained | DQ IQ OQ PQ Full Guide
Can You Pass This OPRA Mock Test 2025? | Pharma 2025 Exam Readiness Challenge
System Suitability Test in HPLC – Fully Explained with Example | USP, FDA, cGMP Guidelines 2025
21 CFR Structure Explained | FDA Regulations for Pharma, Biologics & Medical Devices
USP 〈1079.5〉 Transportation Lane Temperature Mapping & Qualification Explained
FDA CSA Guidance 2025 Explained | Computer Software Assurance Approach & Implementation I CSA
Data Integrity in Pharma: Compliance Violations & Their Consequences Explained
Top 5 Data Integrity Breaches in Pharma | Causes, Examples & Solutions Explained
Why ‘Human Error’ Isn’t the Root Cause in Pharma | Use Error, Root Cause Analysis & GMP Compliance
How to Maintain Data Integrity in Pharma Cloud Systems | ALCOA+ & Compliance Guide (2025)
How to Respond When FDA Inspectors Arrive Unannounced | QA & Facility Readiness for Pharma Sites
EudraLex Volume 4 Chapter 1 Draft Update (2025) | Pharmaceutical Quality System Explained
USP Draft 〈1029〉 (2025) | Good Documentation Guidelines & Data Integrity Explained
USP 1058 Draft (July 2025) | Analytical Instrument Qualification Updates, Compliance & Impact
EU Annex 22 Draft (AI in GMP) Explained | EudraLex Vol. 4 2025 Update
EU GMP Chapter 4 Draft (2025) | What’s New in Documentation & Compliance Updates
EU Annex 11 Draft 2025 Update Explained | What’s New in Pharma Compliance & Computerized Systems
Pharma Calculations: License Exam Math Hacks & Shortcuts | Drug dosage calculations | OPRA | NAPLEX
Cleaning Validation in Pharma | Basics, Guidelines & Examples
Stability Studies in Pharma | ICH Guidelines Explained (Q1A–Q1F) | Best for learning
Quality by Design (QbD) in Pharma | Fundamentals Explained for Students & Professionals
Top 5 OPRA Exam Mistakes by International Students | How to Pass OPRA 2025-2026 (Ex-KAPS)
How to Pass OPRA (ex-KAPS) Exam-2025 | OPRA Full Syllabus & Study Plan | Study Resources + Strategy