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.

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!

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.

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.