Pharmig Europe – 2nd Annual Conference

30th June & 1st July - Leiden

Member Fee £800.00 (Join Now) / Non-Member Fee £1,000.00

Please note:
We do not currently accept AMEX payments via the website. Please do contact the Pharmig office for payments using AMEX – info@pharmig.org.uk

Pharmig Europe 2nd Annual Conference
Hot Topics in Pharmaceutical Microbiology 30th June & 1st July – Corpus Congress Centre, Leiden, Netherlands
NOTE: We are offering early bird. More information can be found on the attached agenda (click here)

Attend and listen from expert presenters covering

Setting the scene as to why we are all here for the next two days
David Keen – Director Pharmaceutical Microbiology, Ecolab & Pharmig Chairman

Endotoxin and pyrogen detection: The regulatory framework in the EU and globally
Alessandro Pauletto – Scientific & Regulatory Subject Matter Expert, bioMérieux

A decade of alternative micro method implementation: Lessons learned and new horizons
Marja Claassen – Microbiology Consultant, Biolumnis

Approach for validation microbial identification methods: primary and limited validations
Marie- Laurence Baille – Senior Microbiology Specialist, MSD Netherlands

Routine environmental monitoring and the path to digitalisation or digitisation
John Brett – Document Control Specialist, QC Microbiology Industrial Affairs, Sanofi

Review of my time in industry: What has changed – what hasn’t. The good, bad, and the ugly
Hans Noordergraaf – Consultant (and recently retired Senior Microbiological Expert, Abbott Biologicals B.V)

Environmental monitoring qualification challenges: Sharing real regulatory experiences
Patrick Nieuwenhuizen – Managing Director, Paradigm Pharmaceutical Quality Consultancy

Humans as a source of contamination: What real data is telling us
Christian Scheuermann – Associate Director, Accugenix Global Technical Services

Microorganisms on the Plate: The Good, the Bad, and the … Objectionable?
Frank Mertens – Laboratory Consultant, Saercon

PDA T33 technical – update on new sections and recommendations for using statistics when validating any RMM with actual data as an example of how to calculate accuracy, LOQ, etc., using the TR guidance
Michael Miller – VP – Scientific & Regulatory Affairs, Spore.Bio

We have a range of discounts on offer if your company is sending 2 or more attendees from the same site.

Please click here for the current agenda, booking form, and fees

Additional information

Date