Good Distribution Practices (GDP-GMP)

Course Feature
  • Cost
    Paid
  • Provider
    Udemy
  • Certificate
    Paid Certification
  • Language
    English
  • Start Date
    2022-03-06
  • Learners
    No Information
  • Duration
    No Information
  • Instructor
    Ruben Alonso
Next Course
4.3
209 Ratings
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.
Show All
Course Overview

❗The content presented here is sourced directly from Udemy 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 course provides learners with the knowledge and understanding of Good Distribution Practices (GDP-GMP). Learners will gain an understanding of the concepts that every employee in the pharmaceutical distribution industry must know and comply with. They will also learn about the main departments and processes involved in a pharmaceutical distribution company. Upon completion of the course, learners will be able to understand the importance of the GDPs and the requirements which will help them improve their daily work, use it in a job interview or in a future position in the distribution of medicines sector. Lifetime access to the course and future updates, personalized support and answers to all questions and doubts, a certificate in “Good Distribution Practices” from Udemy, supportive documentation for their knowledge and questionnaires for practice, and a money-back guarantee in the first 30 days are all included.

Course Syllabus

Presentation & Introduction

Quality Management

Personnel

Premises and Equipment

Documentation

Operations

Complaints, returns, suspected falsified and recalls

Outsourcing

Self-inspections

Transportation

Others

Show All
Recommended Courses
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.
data-integrity-requirements-for-pharmaceuticals-12914
Data Integrity requirements for Pharmaceuticals
3.6
Udemy 164 learners
Learn More
This course provides a comprehensive understanding of the data integrity requirements for pharmaceuticals. It covers topics such as GMP principles, FDA and European inspector citations, US Warning Letters and EU Non-Compliance Reports, and international authority guidelines. Learners will gain an understanding of the data integrity requirements of a GMP regulated laboratory in pharmaceutical organisations and contract labs, and how laboratory personnel can ensure compliance and be able to defend their positions. The course also covers basics in data integrity and audit trail review, as well as the differences between good documentation Practices requirements and data integrity requirements. Specialised sessions focus on data integrity requirements for analytical laboratories and Microbiology laboratories. Join this course to gain a comprehensive understanding of data integrity requirements for pharmaceuticals.
computer-aided-drug-design-cadd-from-a-to-z-12915
Computer Aided Drug Design (CADD) from A to Z
4.2
Udemy 117 learners
Learn More
This course provides a comprehensive overview of Computer Aided Drug Design (CADD) from A to Z. It is suitable for anyone who wants to learn the basics and concepts of drug discovery and design drugs from scratch. Learners will gain an understanding of the relationships between physico-chemical properties of drugs and their biological activities, as well as the types of interactions between drugs and receptors. They will also be familiar with modern techniques such as computer-based methods of quantitative structural activity relationship QSAR and molecular graphics. This course covers all aspects of drug discovery, from sources of lead compound to drug latentiation (prodrug), and is perfect for anyone looking to gain a comprehensive understanding of CADD.
Favorites (0)
Favorites
0 favorite option

You have no favorites

Name delet
arrow Click Allow to get free Good Distribution Practices (GDP-GMP) courses!