Pharma

Impurities in active ingredients, excipients, medicinal products and packaging materials

Master Cell Bank is not only the starting point of GMPs but also the starting point of the manufacturing process of therapeutical recombinant

What is meant by “Contamination Control Strategy”? A complex system of measures designed to minimize the risk!

 What is meant by “Contamination Control Strategy”?

Mastering Dissolution Testing: From Basics to Advanced Techniques

Gain invaluable insights into the development, regulation, and deployment of AI-powered medical devices

Managing CMOs with condence, insight and understanding

Pharmaceutical companies and patients/users interact through theInternet,Social media,and two-way communication.

Pharmaceutical companies and patients/users interact through theInternet,Social media,and two-way communication.

Understand how to qualify scale-down models

The Entry Level CMC Masterclass covers the general requirements for small molecules and biologics.

Microbiological contaminations can occur on many levels.

Microbiological contaminations can occur on many levels.

From regulatory compliance to technical innovation, from financial scrutiny to operational efficiency

Current developments for impurities in small molecule APIs and respective medicinal products

QbD concept, process validation, and regulatory requirements!

How to design and implement the systems your company needs.

The latest revision to ICH GCP

Implementation of Quality by Design principles.

Implementation of Quality by Design principles.

Key elements for a successful development of a drug product analytical development

This online masterclass gives practical examples from method validation and method transfer.

Key points for successful development and registration of products in US

Development and validation of bioassays

Development and validation of bioassays

Beyond Child's Play

Beyond Child's Play

The Entry Level CMC Masterclass covers the general requirements for small molecules and biologics.

Paving the Way from Development to Lifecycle Management

The training aims to generate a common understanding of how to best interlink two areas and create highly efficient processes.

A comprehensive overlook on benefit risk assessment in PSUR and RMP

Connection between risk management with PBRERs and benefit-risk assessment and tools

Mastering Dissolution Testing: From Basics to Advanced Techniques

Today, process validation comprises three main steps:

Key points for successful development and registration of your pharmaceutical products