Cleaning Fundamentals for the Pharmaceutical Industry Online Training Course Demo

Course Feature
  • Cost
    Free
  • Provider
    Youtube
  • Certificate
    No Information
  • Language
    English
  • Start Date
    2016-06-13
  • Learners
    No Information
  • Duration
    No Information
  • Instructor
    ISPE
Next Course
3.0
1,688 Ratings
This online training course provides a comprehensive overview of Clean-in-Place (CIP) systems for the pharmaceutical industry. Participants will gain an understanding of engineering concepts, principles, and integration of CIP systems, Clean-out-of-Place (COP) systems, or immersion parts washers. The course will focus on the dynamics of CIP and COP technologies, with an emphasis on selecting the right cleaning chemistries for specific soil residues. Manual cleaning practices will also be discussed. This course is ideal for those looking to gain a better understanding of the fundamentals of cleaning in the pharmaceutical industry. Click now to learn more about this comprehensive online training course.
Show All
Course Overview

❗The content presented here is sourced directly from Youtube platform. For comprehensive course details, including enrollment information, simply click on the 'Go to class' link on our website.

Updated in [July 27th, 2023]

This online training course provides an overview of Clean-in-Place (CIP) systems, including design, integration, and selection of cleaning chemicals. Participants will gain an understanding of engineering concepts, principles, and integration of CIP systems, Clean-out-of-Place (COP) systems, or immersion parts washers. The course will focus on the dynamics of CIP and COP technologies, with an emphasis on selecting the appropriate cleaning chemistries for specific soil residues. Additionally, manual cleaning practices will be discussed.

Show All
Recommended Courses
good-distribution-practices-gdp-gmp-12910
Good Distribution Practices (GDP-GMP)
4.3
Udemy 209 learners
Learn More
This course provides learners with the knowledge and understanding of Good Distribution Practices (GDP-GMP). It covers the concepts that every employee from the pharmaceutical distribution industry must know and comply with, as well as the main departments and processes involved in a pharmaceutical distribution company. Upon completion, learners will be able to understand the importance of the GDPs and the requirements which will help them improve their daily work. They will also receive lifetime access to the course, personalized support, a certificate in “Good Distribution Practices” from Udemy, supportive documentation, questionnaires for practice, and a money-back guarantee in the first 30 days. This course is perfect for those looking to gain a better understanding of the pharmaceutical distribution industry.
introduction-to-drug-discovery-and-drug-development-12911
Introduction to Drug Discovery and Drug Development
4.1
Udemy 212 learners
Learn More
This course, Introduction to Drug Discovery and Drug Development, is perfect for those looking to expand their career knowledge into the pharmaceutical industry or aspiring pharmaceutical scientists and clinical project coordinators. It provides a deep understanding of the science behind drug discovery, development, clinical trials, alternative medicine, generic and innovator drugs, and regulatory affairs. Through real-life examples, you'll learn why theories work and how to apply them in your daily life. By the end of the course, you'll have a comprehensive understanding of the pharmaceutical industry. Don't miss out on this opportunity to become an expert in drug discovery and development!
good-laboratory-practices-12912
Good Laboratory Practices
4.5
Udemy 176 learners
Learn More
This course on Good Laboratory Practices will provide a comprehensive overview of data integrity in analytical and microbiology laboratories, as well as analytical method validations, stability studies, and human error investigations. Attendees will learn about FDA/EU Citations, ALCOA+ concept, audit trails in microbiology, and more. They will also gain an understanding of QBD approach, ICHQ14, ICHQ2(R1), and revalidation criteria. This course is essential for anyone looking to gain a better understanding of good laboratory practices.
part-11-compliance-for-computerised-systems-12913
Part 11 Compliance for Computerised Systems
3.0
Udemy 188 learners
Learn More
This course provides a comprehensive overview of Part 11 Compliance for Computerised Systems. It covers USFDA 21 CFR Part 11, EUGMP Annex 11, and Data Integrity requirements. Through discussion and learning videos, you will learn how to design systems and processes to ensure compliance, audit preparedness, and common errors to avoid. This course is essential for any pharmaceutical company looking to ensure their computerised systems are Part 11 compliant.
Favorites (0)
Favorites
0 favorite option

You have no favorites

Name delet
arrow Click Allow to get free Cleaning Fundamentals for the Pharmaceutical Industry Online Training Course Demo courses!