Events, Webinars and Deadlines

Our calendar informs on industry events, upcoming compliance deadlines, as well as new Obelis webinars.

  • The Critical Role of the Responsible Technical Person

    2026 is a critical year for cosmetic compliance - and the Responsible Technical Person is at the center of it.Join our 60-minute LIVE webinar to discover how to safeguard your products, avoid regulatory risks, and implement GMP with ISO 22716. ✅ GMP Essentials: key principles for cosmetic products✅ RTP Responsibilities: legal and operational must-knows✅ Practical Tips: ensure compliance efficiently✅ Expert Insights: from Sandra Ferretti, CCO at Obelis Group, and Selim Erol,…

  • ON-DEMAND WEBINAR: Food Supplements in the EU and UK – a focus on online sales (AMAZON)

    Get a clear and practical overview of the essential rules governing food supplements in the EU and UK. This on-demand webinar walks you through the core legislation and compliance requirements every Food Business Operator (FBO) must know.Webinar highlights :✅ Regulation (EC) 178/2002 – General Food Law✅ Brexit and its impact on labeling & notifications✅ Compliance challenges when selling…

  • Winning with IVDR: Compliance Strategy, Class C Pathways & NB Engagement

    The IVDR transition is reshaping how IVD manufacturers approach compliance, evidence, and certification. This session will guide you through the most critical elements of the journey, from transition timelines and legacy provisions, to EUDAMED and UDI requirements, and what they mean in practice. We will also dive into Class C classification and conformity assessment pathways,…

  • EUDAMED Readiness for MDR & IVDR: Registration Obligations and Timelines

    With EUDAMED obligations becoming enforceable from 28 May 2026, manufacturers and economic operators should already be preparing for upcoming registration and compliance requirements under MDR & IVDR. During this expert-led session, our speakers will provide practical insights into the EUDAMED regulatory framework, key timelines and deadlines, affected economic operators, MDR & IVDR registration requirements including…

  • EU & UK Detergents Market Access: Regulations & Upcoming EU Changes

    With evolving regulatory requirements shaping the detergents market in the EU and the UK, manufacturers and importers must ensure full compliance with applicable frameworks, registration obligations, and upcoming legislative changes. This expert-led session will provide a practical overview of the detergents regulatory landscape across both regions, including key compliance frameworks and requirements. The webinar will…

  • Cosmetic Claims Across Borders: Understanding EU and Turkish Requirements

    Join our webinar to gain practical insights into cosmetic claims and their growing importance in today's cosmetics industry. During this session, we will explore what constitutes a cosmetic claim, why claims have become a critical element of product development and marketing, and the regulatory expectations surrounding their use. Special attention will be given to “free…

  • Think You’re FDA Compliant? California May Require More

    Join our webinar to gain practical insights into the U.S. cosmetic regulatory landscape, with a focus on the relationship between federal requirements under MoCRA and California-specific compliance obligations. During this session, we will provide a brief overview of the Modernization of Cosmetics Regulation Act (MoCRA), including its scope and the distinction between federal and state-level…