{"id":15350,"date":"2026-04-23T08:56:18","date_gmt":"2026-04-23T06:56:18","guid":{"rendered":"https:\/\/www.sciencepharma.com\/news-events\/meet-us-pharmacy-expo-2026-warsaw\/"},"modified":"2026-04-23T08:56:18","modified_gmt":"2026-04-23T06:56:18","slug":"meet-us-pharmacy-expo-2026-warsaw","status":"publish","type":"news-events","link":"https:\/\/www.sciencepharma.com\/zh-hans\/news-events\/meet-us-pharmacy-expo-2026-warsaw\/","title":{"rendered":"Meet us at Pharmacy Expo 2026 in Warsaw!"},"content":{"rendered":"<p style=\"text-align: justify;\">We will be at <strong>Pharmacy Expo 2026<\/strong> taking place from <strong>May 5\u20137<\/strong> in <strong>Warsaw<\/strong>, <strong>Poland<\/strong>. This pharmaceutical industry event brings together stakeholders from across the pharma, biotechnology, and healthcare sectors.<\/p>\n\n\n<div style=\"height:29px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<h2 class=\"wp-block-heading\"><strong>Expert Lectures by SciencePharma<\/strong><\/h2>\n\n\n<p>Throughout the event, our experts will deliver three lectures covering key stages of the <strong>pharmaceutical product lifecycle<\/strong> from early development to <strong>market authorization and post-approval responsibilities<\/strong>.<\/p>\n\n\n<div style=\"height:37px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<h2 class=\"wp-block-heading\"><strong>Lecture 1: The Pathway from Drug Candidate to Obtaining Market Authorization \u2013 A Regulatory Roadmap<\/strong><\/h2>\n\n\n<p><strong>Speaker:<\/strong> Joanna Pawlak, PhD<br \/><strong>Date:<\/strong> Day 1 \u2013 May 5 | 12:30\u201313:15<\/p>\n<p>This session provides a practical overview of the <strong>EU drug development and regulatory pathway<\/strong>, from early-stage research to <strong>marketing authorization approval<\/strong>.<\/p>\n<p><strong>What will you learn:<\/strong><\/p>\n<ul>\n<li>How to choose the right<strong> Marketing Authorisation pathway<\/strong> for your medicinal product<\/li>\n<li>How product type and formulation influence regulatory requirements<\/li>\n<li>How to plan studies efficiently and avoid unnecessary costs and delays<\/li>\n<li>How to increase the chances of a successful registration outcome<\/li>\n<\/ul>\n\n\n<div style=\"height:32px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<h2 class=\"wp-block-heading\"><strong>Lecture 2: Marketing Authorization Holder\u2019s Responsibilities in the EU<\/strong><\/h2>\n\n\n<p><strong>Speaker:<\/strong> Joanna Popio\u0142kiewicz, PharmD<br \/><strong>Date:<\/strong> Day 2 \u2013 May 6 | 10:30\u201311:30<\/p>\n<p>This lecture focuses on the <strong>role<\/strong> and <strong>responsibilities<\/strong> of the <strong>Marketing Authorization Holder<\/strong> (MAH) within the EU, with emphasis on managing a medicinal product after it has been granted marketing authorization.<\/p>\n<p>What will you learn:<\/p>\n<ul>\n<li>The scope of MAH responsibilities across the full product lifecycle, from authorization to maintenance on the market<\/li>\n<li>Regulatory compliance obligations, including management of variations and post-authorization changes<\/li>\n<li>Requirements related to product quality and supply chain oversight (GMP and distribution control)<\/li>\n<li>How pharmacovigilance systems are implemented and adverse events are reported and monitored<\/li>\n<li>Responsibilities for maintaining and updating product documentation (SmPC, labeling, patient leaflets)<\/li>\n<li>How patient safety and ongoing market surveillance are ensured in practice<\/li>\n<\/ul>\n\n\n<div style=\"height:43px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<h2 class=\"wp-block-heading\"><strong>Lecture 3: Know the Market, Find the Partner \u2013 Market Analysis and Distributor Search for Medicinal Products<\/strong><\/h2>\n\n\n<p><strong>Speaker:<\/strong> Anna Bie\u0144kowska, PhD<br \/><strong>Date:<\/strong> Day 3 \u2013 May 7 | 12:00\u201312:45<\/p>\n<p><strong>Market analysis<\/strong> is a critical foundation for successful medicinal product launch and expansion, as it helps ensure decisions are based on real market conditions rather than assumptions. It enables a clear understanding of competitive environment, access barriers, and partnership opportunities, supporting more effective and lower-risk market entry strategies.<\/p>\n<p><strong>What will you learn:<\/strong><\/p>\n<ul>\n<li>The session will explain which factors should be considered when analysing a market, from the presence of already registered products, through the competitive landscape and MAH strategies.<\/li>\n<li>We will talk on importance of analysis of competitive registered products, their Rx\/OTC classification, reimbursement status, pricing and sales volumes, as well as risks such as parallel import and product shortages.<\/li>\n<li>Based on these insights the informed decisions on market entry can be made involving proper launch planning, portfolio expansion, and distribution partner selection.<\/li>\n<\/ul>\n\n\n<div style=\"height:40px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<h2 class=\"wp-block-heading\"><strong>Visit SciencePharma at Booth B1.41<\/strong><\/h2>\n\n\n<p>We invite you to visit <strong>us at Booth B1.41<\/strong> during the event. Our team will be available to discuss:<\/p>\n<ul>\n<li><strong>Regulatory strategy and EU market authorization<\/strong><\/li>\n<\/ul>\n<p>Insights from Principal Consultants and Senior Team Leads in Regulatory Affairs, with deep expertise in nonclinical and clinical development.<\/p>\n<ul>\n<li><strong>Nonclinical and clinical development support<\/strong><\/li>\n<\/ul>\n<p>Guidance from Heads and Deputy Heads of Nonclinical &amp; Clinical, supporting efficient development planning and regulatory alignment.<\/p>\n<ul>\n<li><strong>Operational regulatory affairs<\/strong><\/li>\n<\/ul>\n<p>Practical support from Senior and Operations Consultants in RA, including dossier preparation, submissions, and interactions with regulatory authorities.<\/p>\n\n\n<blockquote class=\"wp-block-quote is-layout-flow wp-block-quote-is-layout-flow\">\n<blockquote class=\"wp-block-quote is-layout-flow wp-block-quote-is-layout-flow\">\n<p>Join SciencePharma in Warsaw and take part in <strong>Pharmacy Expo 2026<\/strong>!<\/p>\n\n\n\n<p>Generate your free ticket to the trade fair <a href=\"https:\/\/pharmacyexpopoland.com\/en\/registration\/\">here<\/a>.<\/p>\n<\/blockquote>\n\n\n\n<p><\/p>\n<\/blockquote>\n","protected":false},"excerpt":{"rendered":"<p>We will be at Pharmacy Expo 2026 taking place from May  [&hellip;]<\/p>\n","protected":false},"featured_media":15344,"template":"","meta":{"inline_featured_image":false},"typ":[],"class_list":["post-15350","news-events","type-news-events","status-publish","has-post-thumbnail","hentry"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v26.8 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Meet us at Pharmacy Expo 2026 in Warsaw! 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