Pharma Packaging & Labelling processes play significant roles in preserving medicinal products’ quality, promoting safe use, patient adherence and responsible distribution. With various risks threatening drug supply chain integrity (drug traceability, counterfeiting, medication errors, supply shortage), regulatory guidance and compliance technologies governing the P&L procedures across jurisdictions are transforming and becoming increasingly sophisticated. This V-Forum offers global insights into and practical guidelines for ensuring P&L compliance throughout manufacturing, artwork, drug registration and distribution processes. Attendees will revise important global & regional regulations relating to P&L, how GMP-compliant artwork processes & technologies maximize drug supply chain integrity as well as disputes related to drug P&L quality. Case studies including OTC, Biosimilars, Combination products, APIs will also be examined in detail to offer attendees practical case studies in real-world setting.
Meet our professonals
Packaging & Development
Mankind Research Centre
World Packaging Organisation
Head - Pkgg Tech Services
Head of Packaging Development & Commercial Device Engineering
Assistant General Manager
Head Global Packaging Strategy - OSD
Product Manager Coordinator
Marchesini Group S.p.A.
Chief Operating Officer
Perigord Life Science Solutions
Business Development Executive
Sr. Manager, Global Labeling and Graphics
BioMarin Pharmaceutical Inc.
Sales Manager Global Pharmaceutical Accounts
Regional Sales Director
Schlafender Hase GmbH
Strategic Pharmaceutical Executive EMEA
Prior to Pharma Packaging and Regulatory Content, I spent 15 years on the product side in PLM (Product Lifecycle Management) working for companies.
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