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Pharmatalks
India
Приєднався 21 січ 2022
Welcome to Pharmatalks!
In the pharmaceutical industry, compliance with Good Manufacturing Practices (GMP), regulatory requirements, and quality control standards is crucial for ensuring the safety and efficacy of medications. At Pharmatalks, our mission is to provide you with comprehensive guidance on the latest developments, best practices, and regulations in the pharmaceutical industry.
Our channel covers a wide range of topics, including:
GMP : From facility design to equipment validation, we'll guide you through the essential elements of good manufacturing practices.
Pharmaceutical industry : Learn about the importance of quality control and assurance in ensuring the safety and efficacy of pharmaceutical products.
Subscribe to Pharmatalks today and stay ahead of the curve in the pharmaceutical industry!
In the pharmaceutical industry, compliance with Good Manufacturing Practices (GMP), regulatory requirements, and quality control standards is crucial for ensuring the safety and efficacy of medications. At Pharmatalks, our mission is to provide you with comprehensive guidance on the latest developments, best practices, and regulations in the pharmaceutical industry.
Our channel covers a wide range of topics, including:
GMP : From facility design to equipment validation, we'll guide you through the essential elements of good manufacturing practices.
Pharmaceutical industry : Learn about the importance of quality control and assurance in ensuring the safety and efficacy of pharmaceutical products.
Subscribe to Pharmatalks today and stay ahead of the curve in the pharmaceutical industry!
Secrets of BMR - Batch Records
🔍 Unlock the Secrets of BMR (Batch Manufacturing Records)! 🔍
Ever wondered what goes on behind the scenes in product manufacturing? Batch Manufacturing Records (BMR) keep everything in check, ensuring quality, safety, and compliance with every batch produced. 📋✨
In this video, we’ll cover:
What BMRs are and why they’re essential
Key elements in a BMR
How BMRs support quality and regulatory standards
The role of BMRs in troubleshooting and audits
📽️ Dive into the world of BMR and understand why they’re a game-changer for the industry!
0:09 Introduction
3:51 Section 1: Setting Up a BMR
6:04 Section 2: Steps in Creating a BMR
8:35 Section 3: Specific Documentation Requirements
10:41 Section 4: Using the BMR for Compliance
#BatchRecords #ManufacturingSecrets #QualityControl #PharmaStandards #Compliance #BMR #BatchManufacturing
Ever wondered what goes on behind the scenes in product manufacturing? Batch Manufacturing Records (BMR) keep everything in check, ensuring quality, safety, and compliance with every batch produced. 📋✨
In this video, we’ll cover:
What BMRs are and why they’re essential
Key elements in a BMR
How BMRs support quality and regulatory standards
The role of BMRs in troubleshooting and audits
📽️ Dive into the world of BMR and understand why they’re a game-changer for the industry!
0:09 Introduction
3:51 Section 1: Setting Up a BMR
6:04 Section 2: Steps in Creating a BMR
8:35 Section 3: Specific Documentation Requirements
10:41 Section 4: Using the BMR for Compliance
#BatchRecords #ManufacturingSecrets #QualityControl #PharmaStandards #Compliance #BMR #BatchManufacturing
Переглядів: 130
Відео
Top Pharma Production Interview Questions to Ace Your Job!
Переглядів 11914 годин тому
Ace Your Pharma Production Interview! 🚀 Thank you for tuning in! In today’s video, we’ll help you prepare for your next pharmaceutical manufacturing interview with top questions and insightful answers. Whether you’re new to the industry or looking to advance your career, these questions cover essential topics that hiring managers look for. 🎯 What We Covered in This Video: 1. Understanding GMP S...
Top 50 Pharma Interview Questions on Liquid Dosage Forms (Solutions & Suspensions)
Переглядів 191День тому
Welcome to PharmaTalks! In this video, we dive into the Top 50 most frequently asked questions on liquid dosage forms for pharma interviews, specifically focusing on solutions and suspensions. Whether you're preparing for a role in formulation, quality control, or manufacturing, mastering these questions will give you a strong foundation to ace your next interview. We cover a wide range of topi...
Understanding & Managing Deviations in Pharma | Essential Guide to Compliance
Переглядів 150День тому
In the pharmaceutical industry, managing deviations effectively is crucial to ensuring product quality, regulatory compliance, and patient safety. 📊 Deviations happen more often than you think-whether due to human error, equipment malfunctions, or unexpected events. That’s why it's essential to understand and address deviations in a systematic, compliant way. In this video, we’ll cover: What de...
Guide to Excel Spreadsheet Validation
Переглядів 623День тому
Here is a Useful Guide to Excel Spreadsheet Validation Step 1: Develop Functional Requirements Step 2: Develop the Excel Spreadsheet Application Step 3: Qualification Testing Step 4: Execute Qualification Protocols Step 5: Prepare Final Report Watch Full Video to know main point related to #Excel #Spreadsheet #Validation
How does GMP apply to the pharmaceutical industry?
Переглядів 12714 днів тому
0:09 What is GMP in the Pharmaceutical Industry? 1:12 Why is Quality Management Important in GMP? 2:09 Who are the Key Personnel in GMP? 3:08 Where are GMP Regulations Applied? 4:04 How is Production Controlled Under GMP? 5:03 What are the Requirements for Materials in GMP? 5:56 Why is Sanitation and Hygiene Crucial in GMP? 6:52 How are Equipment and Processes Validated in GMP? 7:55 What is the...
Top 🧪 lab assistant 🗣️ interview questions and Answers
Переглядів 23014 днів тому
0:14 Why do you want to work as a lab assistant? 0:25 What lab equipment are you familiar with? 0:40 How do you handle repetitive tasks? 0:53 Describe a time when you had to follow strict procedures. 1:08 How do you ensure accuracy in your work? 1:24 Have you ever handled hazardous materials? 1:39 How do you handle stressful situations in the lab? 1:52 What do you do if you make a mistake? 2:05...
🎥 50 Basic HPLC Interview Questions | PharmaTalks 🎥
Переглядів 63514 днів тому
0:06 HPLC Interview Questions and Answers 0:13 What is HPLC? 0:35 What is the principle of HPLC? 1:00 What is the difference between normal-phase and reverse-phase HPLC? 1:27 What are the main components of an HPLC system? 1:53 What is a stationary phase in HPLC? 2:15 What is the mobile phase in HPLC? 2:33 What are the common detectors used in HPLC? 2:55 What is the purpose of the HPLC column? ...
Most common Tablet defects , PROCESS and FORMULATION RELATED CAUSES
Переглядів 26414 днів тому
main tablet defects that can occur during the coating stage and best way to resolve them When it comes to the manufacturing of tablets, the coating process plays a critical role in ensuring product quality and effectiveness. However, defects during the coating stage can lead to serious issues, impacting both functionality and appearance. In today’s video, we’ll explore common coating defects an...
Mastering the CAPA Process: Preventing & Resolving Quality Issues in Pharma
Переглядів 19721 день тому
5 fundamental steps in the CAPA (Corrective and Preventive Action) process: Detection: Identify and document the problem, including details like who, what, when, and where, with risk analysis determining the urgency. Investigation & Root Cause Analysis: Investigate the issue to find its root cause using methods like brainstorming or flowcharts. Proposed Corrections: Implement corrective actions...
Top 20 Most In-Demand Jobs in Pharma & Medical Industry
Переглядів 12021 день тому
0:00 Top 20 Most In-Demand Jobs in Pharma & Medical Industry 0:09 Clinical Research Associate (CRA) 0:43 Regulatory Affairs Specialist 1:16 Pharmacovigilance Officer 1:51 Medical Science Liaison (MSL) 2:21 Quality Assurance (QA) Manager 2:53 Biostatistician 3:23 Clinical Pharmacologist 3:51 Formulation Scientist 4:20 Process Development Scientist 4:48 Research Scientist (Drug Discovery) 5:16 Re...
🖥️ Computer System Validation Specialist CSV🖲️ Interview Questions and Answers
Переглядів 74221 день тому
0:00 40 interview questions for a Computer System Validation (CSV) specialist role 0:13 What is Computer System Validation (CSV)? 0:36 Why is CSV important in regulated industries? 1:03 What regulatory bodies govern CSV in the pharmaceutical industry? 1:29 What are GxP guidelines? 1:58 What is 21 CFR Part 11? 2:27 What is the difference between verification and validation? 2:53 Can you explain ...
7 Critical Components You Must Qualify and Control in HPLC for Accurate Results
Переглядів 37128 днів тому
In today’s video, we dive into the seven essential components that must be qualified in High-Performance Liquid Chromatography (HPLC) systems to ensure compliance with EDQM guidelines. These qualifications are critical for achieving accurate, precise, and reliable results in pharmaceutical analysis. Below is a summary of each component, its role, and the key experimental methods involved in the...
Top 50 Essential Tablet Production Questions Answered | Pharma Industry Insights
Переглядів 83128 днів тому
0:00 50 interview questions about tablet production in the pharmaceutical industry 0:06 What is tablet manufacturing? 0:23 What are excipients in tablet production? 0:41 What are the main stages of tablet production? 1:03 What is granulation? 1:21 What is the purpose of tablet coating? 1:38 What are the types of tablet coating? 2:01 Why is tablet hardness important? 2:21 What is dissolution tes...
Stay Compliant with USP 1058 in 2024 | Analytical Instrument Qualification | Pharmacopeia
Переглядів 199Місяць тому
0:00 How Can Your Lab Stay Compliant with USP 1058 in 2024? 0:05 Overview of USP 1058 and Its Importance 0:25 Key Changes in the 2017 Version of USP 1058 0:44 USP 1058 Instrument Groups A, B, and C 1:37 The Role of Analytical Instrument Qualification in Data Integrity 2:22 How to Achieve Compliance with USP 1058 in 2024 3:48 The Future of AIQ and USP 1058 Key Changes in the 2017 Version of USP ...
Quality Assurance Interview Questions & Answers for #Pharma #Job Seekers
Переглядів 1,3 тис.Місяць тому
Quality Assurance Interview Questions & Answers for #Pharma #Job Seekers
Qualification vs. Validation in the Pharma Industry
Переглядів 452Місяць тому
Qualification vs. Validation in the Pharma Industry
Introduction to Cleaning Validation: Ensuring Compliance in Pharmaceutical Manufacturing
Переглядів 428Місяць тому
Introduction to Cleaning Validation: Ensuring Compliance in Pharmaceutical Manufacturing
Top GMP Interview Questions and Answers for Job Seekers | Land Your Pharma Job
Переглядів 722Місяць тому
Top GMP Interview Questions and Answers for Job Seekers | Land Your Pharma Job
Laboratory Method Verification: Essential Steps and Guidelines | PharmaTalks
Переглядів 276Місяць тому
Laboratory Method Verification: Essential Steps and Guidelines | PharmaTalks
Stability Testing for Pharmaceutical Products | Complete Guide by PharmaTalks
Переглядів 366Місяць тому
Stability Testing for Pharmaceutical Products | Complete Guide by PharmaTalks
Quality Assurance and Quality Control in Microbiology Laboratory | Best Practices Explained
Переглядів 552Місяць тому
Quality Assurance and Quality Control in Microbiology Laboratory | Best Practices Explained
Top 40 Analytical Method Validation Interview Questions & Answers | Expert Guide
Переглядів 1,4 тис.Місяць тому
Top 40 Analytical Method Validation Interview Questions & Answers | Expert Guide
Testing Procedures and #Quality Assurance in #microbiology Laboratory
Переглядів 247Місяць тому
Testing Procedures and #Quality Assurance in #microbiology Laboratory
Essential Guidelines for #Pharmaceutical #Microbiology Labs
Переглядів 447Місяць тому
Essential Guidelines for #Pharmaceutical #Microbiology Labs
GMP Principles: The 5 P's of Good Manufacturing Practice
Переглядів 126Місяць тому
GMP Principles: The 5 P's of Good Manufacturing Practice
Main Parts of EU GMP Annex 1 Guideline in Simple Language
Переглядів 291Місяць тому
Main Parts of EU GMP Annex 1 Guideline in Simple Language
Key terms related to validation of an analytical method
Переглядів 1,1 тис.Місяць тому
Key terms related to validation of an analytical method
How PDCA , Pharmaceutical Product Lifecycle Management and GMP help Pharmaceutical Quality System
Переглядів 106Місяць тому
How PDCA , Pharmaceutical Product Lifecycle Management and GMP help Pharmaceutical Quality System
What is Definition of Risk , Quality Risk Management
Переглядів 216Місяць тому
What is Definition of Risk , Quality Risk Management
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Hi Dear Pharmatalks Friend Here is the link of GMP FREE Course pharmuni.com/courses/6/introduction-to-good-manufacturing-practices-gmp
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I have a question about CSV , please mention best references related to CSV and GAMP 5
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🚀Got questions about preparing for a lab assistant interview? Want to share your own tips or experiences? Drop a comment below! Let's support each other and ace those interviews together!🚀
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Hi Dear Pharmatalks Friend Here is the link of GMP FREE Course pharmuni.com/courses/6/introduction-to-good-manufacturing-practices-gmp please send your questions and your question regards to pharma industry here in comments section We will respond you as soon as possible
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