GMP Fundamentals Bundle Series - Limited Offer

On Demand Training

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ISPE’s On Demand training includes recorded conference sessions, instructional lead courses, webinars and e-learning modules to help you expand your skills and knowledge from the comfort of your desk.

GMP Fundamentals: Eleven-Part Bundle Series

GMP Fundamentals: Eleven-Part Bundle Series

Obtain a 10% Savings by Purchasing All Eleven Courses

ISPE is presenting an eleven-part series that will focus on the fundamentals of good manufacturing practices (GMPs). The series provides an overview of the regulations pertaining to GMPs and covers topics such as: manufacturing controls, product distribution, plant hygiene, documentation practices, buildings & facilities, organizational structure, and more.

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GMP Fundamentals: Packaging & Labeling Control
GMPs

GMP Fundamentals: Packaging & Labeling Control

In this course, you will learn how to ensure the safety and quality of pharmaceutical products using fundamental principles and best practices. During this course, you will learn about the FDA's pharmaceutical packaging and labeling guidelines. You will gain an understanding of the basics of...
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GMP Fundamentals: Organization and Personnel
GMPs

GMP Fundamentals: Production & Process Controls

This course offers an overview of Good Manufacturing Practices (GMP) for medical product production and process control. You will learn about GMP compliance, product design and development, process validation, control systems, and quality control procedures. Regulatory requirements, including FDA...
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GMP Fundamentals: Quality System
GMPs

GMP Fundamentals: Quality System

To ensure pharmaceuticals meet specifications and regulatory requirements, manufacturers must create, implement, and follow quality systems. A “Quality System” is blueprint for a pharmaceutical manufacturer. It outlines quality philosophies and processes, provides details about how people work...
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GMP Fundamentals: Records and Reports
GMPs

GMP Fundamentals: Records and Reports

In this course, you will learn the various types of documentation and record-keeping practices used in the pharmaceutical industry, and how to establish and maintain clear policies and procedures to ensure compliance with regulatory requirements, and maintain product quality and patient safety...
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GMP Refresher
GMPs

GMP Refresher

Code of Federal Regulations (CFR) states that "Training in current good manufacturing practice shall be conducted by qualified individuals on a continuing basis and with sufficient frequency to assure that employees remain familiar with cGMP requirements applicable to them." This course will provide...
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GMP
GMPs

GxPs for Leadership

This comprehensive course will equip you with the knowledge and skills to ensure GxP compliance and inspection readiness in the pharmaceutical industry. You will thoroughly understand regulatory requirements and learn about management's role in maintaining safety and quality. The course covers...
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ICH Q6A
Quality Management Systems

ICH Q6A: Specifications, Test Procedures, and Acceptance Criteria for New Drug Substances and Products

Delivery Mode: Webinar This course covers testing and quality control requirements in marketing authorization/new drug applications, emphasizing ICH guidelines. It focuses on ICH Q6A, detailing test procedures and acceptance criteria for new drug substances/products to ensure global consistency and...
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ICH Q9(R1)
Quality Management Systems

ICH Q9(R1): Guidelines on Pharmaceutical Risk Management

Delivery Mode: Webinar An introduction to the ICH Q9(R1): Guidelines on Pharmaceutical Risk Management. This lesson covers the fundamentals for assessing and mitigating risks during drug product lifecycles and incorporates the latest requirements from ICH Q9(R1), which was updated in 2023, and...
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Implementation of ICH Q12 Guideline
Quality Management Systems

Implementation of ICH Q12 Guideline

Delivery Mode: Webinar ISPE Team Assists Training Health Canada with Implementation of ICH Q12 Guideline, Technical and Regulatory Considerations for Pharmaceutical Product Lifecycle Management Regulatory Background International Council for Harmonisation’s (ICH) guideline entitled, “Technical and...
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