Introductory

Mastering Quality Management Systems (QMS)

A Quality Management System (QMS) guarantees that products or services consistently fulfill or surpass customer expectations. Emphasizing quality enables organizations to boost customer satisfaction and loyalty, resulting in repeat business and positive feedback. In this fully accredited course, we’ll discuss how implementing a QMS involves several fundamental steps to ensure its effectiveness and success. Each… Continue reading Mastering Quality Management Systems (QMS)

Equipment Qualification in the GxP Environment

Whether your operation is covered by GMP, GLP, or GCP, there is a regulatory requirement to ensure that all equipment used has been properly demonstrated and documented to be functioning properly. Commonly referred to as Installation Qualification, Operational Qualification, and Performance Qualification, IQ/OQ/PQ provides the framework under which this process can be appropriately performed. Overlooking… Continue reading Equipment Qualification in the GxP Environment

Cosmetic Products Development

This fully accredited course will provide a step-by-step guide to the cosmetic product development process, helping you understand technical marketing, formulation, and testing strategies necessary to obtain efficacious, high-quality products. An “ideation-to-product introduction” approach will be presented, with technical and marketing milestones needed to be met during each critical stage of product development. The topics… Continue reading Cosmetic Products Development

Surfactants: Chemistry, Theory,and Application

The high surface tension of water presents challenges to a formulator who attempts to develop products that will properly wet surfaces, disperse pigments, emulsify key components, or even generate or destabilize foam. This accredited course on surfactants (chemistry, theory, mechanism, and application) initially reviews the various types and chemical structures of commercially available surfactants. An… Continue reading Surfactants: Chemistry, Theory,and Application

Rheology: Chemistry, Theory, and Application

We must understand how materials are affected, by their flow behavior, as a result of applied stress forces. This knowledge will allow a formulator to develop products with the best possible outcome considering production, storage, packaging, and application. This intensive, accredited training course on rheology (chemistry, theory, mechanism, and application) reviews the basic principles of… Continue reading Rheology: Chemistry, Theory, and Application

Introduction to Validation Principles, Practices and Requirements

FDA-regulated industries utilize several types of validation to help ensure the quality of their products and to comply with FDA and international regulations and requirements. This training course provides an overview and introduction to Validation principles and requirements. Process validation, Computer System Validation, Cleaning Validation, Methods Validation, Qualifications, and Validations Project Management are all topics discussed in… Continue reading Introduction to Validation Principles, Practices and Requirements

Starches: Fundamentals and Process Applications in Industrial Operations

This comprehensive training course is on the fundamentals of starch science and its applications in various industries. The course will cover the basics of starch chemistry, structure, and properties, and how these properties can be tailored to suit different industrial applications. You can expect to learn about the different types of starches and their functional… Continue reading Starches: Fundamentals and Process Applications in Industrial Operations

Optimization of Powders for Flowability

There are several metrics that formulators use to quantify the flowability of powder blends, including angle of repose, Carr and Hausner ratios, FFC, and flow energies. They all have one thing in common: none will predict whether or not a powder will flow in a hopper. Frequently, powders that are deemed easy flowing exhibit flow… Continue reading Optimization of Powders for Flowability

Introduction to CAPA Management

There have been several form 483s and warning letters being issued to companies by the FDA as it relates to CAPA investigation because of insufficient or incomplete quality systems procedures applicable to Corrective Action and Preventative Action programs(CAPA). Addressing an FDA form 483 with findings associated with CAPA systems must be performed adequately, and completely… Continue reading Introduction to CAPA Management

Introduction to Batch Record Review

Regulatory Agencies require firms to have written procedures in place to document production and process controls, better known as batch records. Additionally, there must be written procedures for a batch record review process to demonstrate compliance. A strong batch record review system is essential to properly document all critical and operational process parameters that go… Continue reading Introduction to Batch Record Review