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Piedad’s presentation focus on the critical requirements for compliance with EU GACP (Good Agricultural and Collecting Practices) and EU GMP (Good Manufacturing Practices) regulations, particularly in relation to the categorization of cannabis-based products as active pharmaceutical ingredients (APIs) or medicines. During her talk, Piedad provide valuable insights into the implementation of an adequate Pharmaceutical Quality System (PQS), highlighting the importance of a risk-based approach. She also discuss the special requirements that apply to controlled substances and how to integrate these into a robust Quality System, ensuring compliance with the stringent regulations governing the industry. With years of experience as a pharmaceutical consultant, Piedad has a profound understanding of the necessary steps for companies—both new and established—to achieve compliance with European regulations for the manufacture and distribution of cannabis-based pharmaceutical products. She share her expertise on navigating the licensing process, particularly regarding the quality standards required during the submission of documentation to regulatory bodies, with a focus on the Spanish Agency of Medicines and Medical Devices (AEMPS). ✨ Follow us on our social networks for more updates: ► LinkedIn: /cannabishuborg ► Instagram: /cannabishub_org ► X: [@CannabisHub_org](https://x.com/CannabisHub_org) ► TikTok: /cannabishub.org #CannabisHub #MedicalCannabis #PharmaceuticalQuality #EUGMP #EUGACP #Compliance #CannabisIndustry #CdaysBilbao