Showing 12601 to 12615 of 21793 results
Viral Clearance MasterClass

Viral Clearance MasterClass

03 - 04 October, 2022

Online Event

This online masterclass will give an overview of the sources and impacts of viral contaminations of biotherapeutics, how to prevent those risks and how to evaluate the capability of the process to remove and/or inactivate potential viruses through viral clearance studies.  Key Elements: Understand the consequences linked to a contamination of mammalian cell cultures and biologicals Understand the regulatory expectations on prev...

  • +3 months
Advanced CMC MasterClass

Advanced CMC MasterClass

05 - 06 October, 2022

Online Event

This training will present Technical and regulatory requirements for developing a medicinal product which are becoming stricter every day, the products themselves become more and more complex.  Key Elements: Understand the different levels of requirements in CMC during the development and post-approval phase. Overview of stability requirements. Understand what are the Essential Requirements for a Drug Substance. ...

  • +3 months
Implementation of ISO 13485 MasterClass

Implementation of ISO 13485 MasterClass

10 - 11 October, 2022

Online Event

Implementation of ISO 13485 MasterClass shall describe the general increase in combination products and in particular products now regulated by both drug and medical device regulation it is important to decide if, when and how ISO13485 should be implemented within your organisation. Key Elements: Medical device quality system requirements and when they apply to medicinal products. Determining whether to implement ISO13485 in the ...

  • +3 months
Advanced Stability Testing of Pharmaceuticals MasterClass

Advanced Stability Testing of Pharmaceuticals MasterClass

10 - 13 October, 2022

Online Event

Advanced Stability Testing of Pharmaceuticals Online MasterClass ill cover the scientific principles of chemical and physico-chemical degradation of active substances and pharmaceutical products as well as the regulatory requirements to establish a retest period or shelf-life. Key Elements:. The Impact of Thermal Energy and Humidity on Degradation. The opportunities for reduced stability studies. The Smart Selection of...

  • +3 months
Pharma Packaging MasterClass

Pharma Packaging MasterClass

11 - 12 October, 2022

Online Event

This practical training Course's goal is to cover the technical and organisational requirements and procedures of pharma and healthcare packaging and technical operations in a 360-degree coverage. Key Elements: The Requirements of pharma and healthcare packaging. The Global Healthcare and Pharma Market. The concept of the ‘human imperative’ and its practical application. The technical implementatio...

  • +3 months
Quality control for ATMPs and Biologics MasterClass

Quality control for ATMPs and Biologics MasterClass

17 October, 2022 - 17 October, 2022

Online Event

You will learn about quality control requirements for Biologics and Advanced Therapy Medicinal Products (ATMPs). Key Elements: Specifications for Biologics and ATMPs Quality Control for Biologics and ATMPs Visit the official website for more information on the MasterClass: https://glceurope.com/events/pharma/quality-control-for-atmps-and-biologics-masterclass...

  • +3 months