Top 5 Must-Attend Pharma Events This Autumn 2025 for Industry Professionals

Emi Lecret • September 23, 2025

World Vaccine Congress Europe 2025

Location: Amsterdam, Netherlands

Date: October 13-16, 2025



🌍 Audience: Vaccine developers, researchers, public health officials, pharma industry leaders
🧠
Focus: Vaccine development, immunization strategies, regulatory updates, global health policies


This annual event held in Amsterdam is a leading platform where vaccine experts, researchers, and industry leaders converge to discuss the latest advancements in vaccine development and public health strategies. Attendees will explore innovative technologies, regulatory updates, and collaboration opportunities aimed at improving global vaccination efforts.


Register to the World Vaccine Congress Europe 2025

CPHI Worldwide 2025


Location: Messe Frankfurt, Allemagne

Date: October 28-30, 2025


🌍 Audience: Pharmaceutical professionals from manufacturing, R&D, supply chain, regulatory affairs worldwide
🧠 Focus: Drug development, manufacturing innovation, regulatory compliance, business networking


Taking place in Frankfurt, Germany, CPHI Worldwide is the largest global pharmaceutical event, bringing together thousands of professionals across the pharma supply chain. This conference offers unparalleled networking opportunities, showcases the latest innovations in drug development, manufacturing, and regulatory compliance, and fosters partnerships between pharma companies worldwide.


Register to CPHI Worldwide 2025

5th World Congress on Rare Diseases & Orphan Drugs

Location: Paris, France

Date: October 16-17, 2025


🌍 Audience: Clinicians, researchers, regulatory authorities, pharmaceutical companies focused on rare diseases
🧠 Focus: Orphan drug development, clinical trials, patient access, rare disease research


Hosted in Paris, France, this congress focuses on the unique challenges and opportunities in treating rare diseases. It gathers clinicians, researchers, and regulatory authorities to discuss orphan drug development, patient access, and clinical trial design, driving forward innovation in this critical yet often overlooked field.

See program and
Register to the 5th World Congress on Rare Diseases & Orphan Drugs

18th International Conference on Pharmaceutics and Drug Safety

Location: Berlin, Germany

Date: October 16-17, 2025


🌍 Audience: Pharma scientists, regulatory professionals, quality assurance experts, academics
🧠 Focus: Drug safety, pharmaceutics, quality control, regulatory challenges


Held in Berlin, this conference is dedicated to advancing knowledge in pharmaceutical sciences and drug safety. Industry experts, regulatory professionals, and academics discuss new approaches to ensuring medicine safety, quality assurance, and regulatory strategies that impact drug development and patient wellbeing.


Register to the 18th International Conference on Pharmaceutics and Drug Safety

7th European Conference on Advanced Clinical Trials and Research

Location: Paris, France

Date: October 23-24, 2025


🌍 Audience: Clinical researchers, regulatory experts, trial sponsors, biomedical scientists
🧠 Focus: Clinical trial methodologies, regulatory frameworks, research innovation, trial efficiency


This Paris-based conference focuses on cutting-edge methodologies and regulatory challenges in clinical trial design and execution. Attendees include clinical researchers, regulatory experts, and sponsors looking to stay ahead of evolving standards, improve trial efficiency, and foster innovation in biomedical research.


Register to the 7th European Conference on Advanced Clinical Trials and Research

This post was written and published by Emi Lecret, French medical writer and pharmaceutical translator

Share

By Emi Lecret September 30, 2025
What is the International Council for Harmonisation (ICH) and Its Guidelines?
By looka_production_118650064 September 18, 2025
Expanding into the French healthcare market requires precision, compliance, and culturally adapted communication . A French medical writer will help you ensure that all content (whether patient-facing or clinician-facing documents) meets the highest standards of clarity and local regulatory compliance . From pharmaceuticals to medical devices, navigating the requirements of the ANSM (Agence Nationale de Sécurité du Médicament et des Produits de Santé) is a must for successful market entry . Partnering with a skilled French medical editor will also ensure your documents resonate with healthcare professionals (HCPs) and patients while adhering to local guidelines.
By Emi Lecret August 19, 2025
In the medical device industry, consistent language across all documents is essential for safety, regulatory compliance, and brand credibility. Harmonized terminology across labeling, clinical guides, and marketing materials ensures your message is clear, accurate, and fully compliant.