Pharmaceutical manufacturing is a critical industry that requires proper and comprehensive training for effective practice.
One of the most important departments in every pharmaceutical factory is the Quality Control (QC) department.
The role of the QC department is to analyze and test every stage of drug manufacturing, from the raw materials to the final product.
Working in the QC department demands a strong understanding of various aspects to improve one's chances of securing a position and advancing in the field.
This course is the first to explain in detail, using simple language and an accessible approach, all the sections of Quality Control management in pharmaceutical factories and the role of each section.
It includes comprehensive details about the functions of each section and the tests conducted at each stage of drug manufacturing.
The course prepares you for any job interview in a pharmaceutical QC department and helps you understand all the tasks and divisions within Quality Control.
Importantly, it is suitable for recent graduates and does not require any prior experience to understand and learn the course content.
The course is appropriate for graduates of all scientific faculties that qualify them to work in pharmaceutical companies, such as pharmacy and science departments.
The course provides a detailed explanation of:
1st section - Raw materials and what should be analyzed in material to approve it
2nd section - Finished products and what characteristics we test
3rd section - Stability section and how to perform stability studies
4th section - Analytical method validation, And how to validate the analysis method
5th section - General chapters and some analytical chemistry concepts important for QC lab
6th section - Instruments used in Quality control lab
16-Mar-2025
Only need to provide PDF files of the contant