An exclusive and prestigious conference, accessible only by invitation, uniting prominent clinical trial executives with forward-thinking suppliers and solution providers.
The 2025 conference will be bigger and better than ever, bringing you 3 days of expertise, comprising of a pre-conference focus day exploring the advances in PFS design for enhanced drug delivery
Permit manufacturers to discuss contemporary challenges to design, supply, transportation, containerizing and packaging of devices while ensuring sustained production, product performance, and sterility assurance in the face of evolving rules and regulations.
The LSX World Congress is Europe's leading partnering, strategy, and investment event, with qualified 1:1 partnering at its core.
The congress typically covers topics such as FDA regulations, compliance strategies, quality assurance, risk management, and ethical concerns in the industry.
Discover the power of connections at the original medical device partnering conference.
The Making Pharmaceuticals Conference and Distributing Pharmaceuticals Conference run concurrently across the two days of the event, with eight theatres in total covering topics across the whole product lifecycle from discovery to distribution.
The conference features expert-led sessions, product showcases, and networking opportunities, covering topics such as regulatory updates, device design, manufacturing, and commercialization.
The future of gene therapy for children and adults with hearing loss, cochlear implants in the hearing health continuum: the US and around the world.
This event provides a platform to discuss main trends, current challenges and futuristic advancements in clinical trials and clinical research occurring in pharma world.
You’ll connect with an incredible gathering of experts and uncover practical advice from industry-leading researchers and executives.
Leading Voice are coming together to create something real—a conference built around connection, learning, and action.
RAPS Euro Convergence is the most comprehensive regulatory affairs conference in Europe, focusing on the latest topics and developments in healthcare products in Europe and beyond
Together, we will tackle the ever- evolving opportunities and challenges for our industry, from innovation and digital transformation to regulatory developments and sustainability.
The summit focuses on partnerships, licensing deals, and innovation in drug development.
This event will offer a unique platform for exploring the latest in regulatory guidance, including updates from the FDA's 2022 draft guidance on human factors.
This seminar offers essential guidance on effectively utilizing the ISO 10993 standards and integrating a robust risk management approach into the biological evaluation process of medical devices.
You hear the latest research discoveries from the experts, learn about technology advances in the field, participate in panel discussions and poster presentations, and build new network.
It focuses on fostering strategic partnerships, licensing opportunities, and collaborations to drive innovation in drug development and bring new therapies to market.
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