Supplier Qualification Audits: Proven Strategies for Effective Preparation
Overview
Are you eager to elevate your supplier management practices and ensure your suppliers meet the necessary standards? Join us for an enlightening webinar on “How to Effectively Prepare for a Supplier Qualification Audit.” Dive into proven strategies for success and unlock the secrets to seamless supplier qualification audits.
During this exclusive event, you will gain valuable insights into the essential steps and best practices required to streamline the supplier qualification audit process. Discover how proper preparation can not only strengthen your supplier relationships but also enhance your supply chain efficiency.
By participating in this webinar, you will arm yourself with practical tips, real-life case studies, and expert advice to excel in your supplier qualification audits. Don’t miss out on this opportunity to enhance your supplier management skills and take a significant step towards mastering the art of supplier qualification audits.
Register now to secure your spot in this informative webinar and embark on a journey towards smoother audits, improved compliance, and enhanced supplier performance. Join us in this insightful session and empower yourself with the knowledge needed to thrive in supplier qualification audits.
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Who Should Attend
- VP, Director, Head, Senior Manager of Quality, Manufacturing,
- R&D of Pharmaceutical companies.
- Skill Level Novice, Intermediate , Expert
Speaker
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Amnon EylathQuality Leader | GMP ExpertAmnon is a seasoned Quality Leader, experienced in the complete life cycle of Biological and Small Molecule drug development: from discovery, through nonclinical and Tox studies, clinical trials, process and method development, GMP manufacturing, validation, regulatory submissions and US/EU/MHRA commercial product approvals.
Amnon has a direct experience with Cell and Gene therapy and with developing and troubleshooting aseptic processes, including design and fabrication of isolators and the implementation and validation of highly effective decontamination and sterilization technology.
He has worked at various capacities in international companies, such as Amgen, Ely Lilly and GenzymeSanofi, as well as at cell therapy companies such as Cellcore Therapies, Histogenics and Minovia Therapeutics. Currently, Head of Quality at Alkeus Pharmaceuticals, responsible for building and leading all GXP Quality Management Systems 9GLP, GMP, GCP, etc.) and GXP compliance oversight. Support of regulatory submissions. Preparation and hosting of health authority inspections.
Amnon is also a volunteer with the PDA (Parenteral Drug Association), Chair for the drafting of Technica Report T-56 (Application of Phase-Appropriate Quality System and cGMP) and co-author for TR-65 Technology Transfer), Prior President of the New England Chapter of the PDA.
Partner
Pharmalane UK
Phone
+44 (0) 203 195 3933Website
https://www.pharmalaneuk.com/PHARMALANE UK Ltd. is an ISO 9001:2015 certified Global Pharmaceutical Consultancy (specialised in GxP audits) registered with the Registrar of Companies for England and Wales, UK, and catering to the clients across the globe.
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