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The Complete Pharmaceutical Production Course

The Complete Pharmaceutical Production Course
Published 4/2023
MP4 | Video: h264, 1280x720 | Audio: AAC, 44.1 KHz
Language: English | Size: 6.95 GB | Duration: 11h 15m
API'S, Formulations, Data Integrity, ALCOA+, cGMP, Packaging, IPQA, QMS


Free Download What you'll learn
Introduction to Pharma Industry-Types of formulations
USFDA Guidelines to be followed and their importance in industry.
cGMP regulations
Good documentation practices, Data Integrity and ALCOA Principles
Importance of Line clearance procedures
Manufacturing of API's
Manufacturing of formulations
Packing of various formulations.
Various equipment's used for packing
Role and importance of IPQA in the manufacturing and packing.
Batch release procedure into market
Requirements
Basic Knowledge on Pharmaceutical industry
Basic level of English
Good quality of internet connection, Desktop /Laptop/Smartphone required(Since dealing with online mode
Description
Pharmaceutical manufacturing is the process of industrial-scale synthesis of pharmaceutical drugs as part of the pharmaceutical industry. The process of drug manufacturing can be broken down into a series of unit operations, such as milling, granulation, coating, tablet pressing, and others.Below topics will cover in this course- Introduction to Pharma Industry-Types of formulations-USFDA Guidelines to be followed and their importance in industry. -USFDA Guidelines to be followed and their importance in industry. -cGMP regulations -Good documentation practices, Data Integrity and ALCOA Principles -Importance of Line clearance procedures -Introduction to manufacturing of APIs -Discussion on various equipment's used in manufacture of APIs—session1. -Discussion on various equipment's used in manufacture of APIs—session2. -Manufacturing process of APIs -Introduction to manufacturing of OSDs -Discussion on various equipment's used in manufacture of OSDs—session1. -Discussion on various equipment's used in manufacture of OSDs—session2. -Granulation processes Day-14: Manufacturing process of Tablets -Manufacturing process of liquids and semisolids -Manufacturing process of capsules -Introduction to manufacturing of sterile formulations, Discussion on clean room conditions -Discussion on various equipment's used in manufacture of steriles -Manufacturing process of various sterile formulations -Introduction to packing of various formulations. -Discussion on various equipment's used for packing-Discussion on various checkpoints during packing -Role and importance of IPQA in the manufacturing and packing.-Batch release procedure into market
Overview
Section 1: Introduction
Lecture 1 Introduction to Pharma Industry-Types of formulations
Lecture 2 USFDA Guidelines to be followed and their importance in industry
Lecture 3 Common GMP deficiencies during sampling and manufacturing
Lecture 4 Common GMP deficiencies during packaging
Lecture 5 Good documentation practices, Data Integrity and ALCOA Principle
Lecture 6 Importance of Line clearance Procedures
Section 2: Manufacturing of API'S
Lecture 7 An Introduction to Manufacturing of API's # Class-1
Lecture 8 Manufacturing of API's - Reactors
Lecture 9 Manufacturing of API's-Centrifuge
Lecture 10 Manufacturing of API's-Driers
Lecture 11 Manufacturing of API's - Tray Dryer, Jet mill & Sifter
Lecture 12 Manufacturing of API's- Blender & API Manufacturing process
Section 3: Manufacturing of Various Formulations
Lecture 13 An Introduction to Manufacturing of Solid Dosage Forms
Lecture 14 Discussion on various equipment's used in manufacture of OSDs—session1
Lecture 15 Discussion on various equipment's used in manufacture of OSDs—session2
Lecture 16 Manufacturing process of Tablets
Lecture 17 Manufacturing process of liquids and semisolids
Lecture 18 Manufacturing process of capsule
Lecture 19 Introduction to manufacturing of sterile formulations, Discussion on clean room
Lecture 20 Discussion on various equipment's used in manufacture of steriles
Lecture 21 Evaluation of tablets
Lecture 22 Introduction to packing of various formulations.
Lecture 23 Discussion on various checkpoints during packing
Lecture 24 Role and importance of IPQA in the manufacturing and packing.
Lecture 25 Batch release procedure into market
Graduate or postgraduate degree in Pharmacy or Pharmaceutical Sciences,Graduate or postgraduate degree in Chemistry,Graduate or postgraduate degree in Life sciences


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https://www.udemy.com/course/the-complete-pharmaceutical-production-course/












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