Over the last few years, the requirements on the assessment of substances that could leach into the drug product over its life cycle have increased significantly. Substances may migrate from different materials and patients may be exposed through different routes of administration. On the other hand, a drug product container-closure system should not release chemicals that can accumulate in the drug product in quantities sufficient to present a risk of toxicity, or affect its stability or efficacy.
Join our workshop to embark on a journey through the pharmaceutical packaging testing. By attending you will be able to implement a successful strategy to ensure the safety of yourproducts.
View event brochure
KEY INFORMATION:
DATE: 20th May 2026
TIME & LOCATION: 9 AM - 5 PM, Doubletree by Hilton Manchester - Piccadilly. One Piccadilly Place, 1 Auburn Street, Manchester, M1 3DG
REGISTRATION FEE: £195
WORKSHOP LANGUAGE: ENGLISH
SPEAKERS:
- Francesco Tessari - E&L Technical Business Manager, Eurofins BioPharma Product Testing Italy
- Daniele Zarini - Project Manager, Eurofins Regulatory & Consultancy Services Italy Srl
- Elenora Lostaglio - Consultant, Eurofins Regulatory & Consultancy Services Italy Srl
DURING THIS WORKSHOP YOU WILL LEARN:
- Regulatory requirements and expectations on E&L
- How to prepare a successful E&L study
- Practical approaches for E&L testing
- Evaluation of E&L data
- Toxicological assessment
- E&L testing for single-use systems
- Container Closure Integrity Testing (CCIT)
REGISTER HERE!
CONTACT: Sophie.Killick@bpt.eurofinseu.com
