The cream of the European life sciences community will be attending this business conference, attracting decision makers from biotech, pharma and MedTech as well as investors, universities, top-notch research institutes, policymakers, and competence providers.
Successfully navigate the EU Clinical Trials Regulation, and more. Topics include: Expectations and responsibilities of UK and EU QPs, Impact of the EU Clinical Trials Regulation and its challenges, How to ensure supply continuity across Europe, ...
Live30 webinars are thirty-minute presentations designed to update you on the latest innovations, applications, and data in a fast yet interactive format.
Developing and commercializing viral vectors for gene therapies is a complex and expensive process. It requires careful consideration of various key elements, including regulatory compliance, process design, specifications, and supply chain strategy. To ensure timely and cost-effective project delivery, it is crucial to understand the critical aspects of this journey and mitigate potential challenges.
Although randomized, controlled clinical trials (RCTs) are the FDA-preferred approach for registrational studies in new drug and biologics development, there are circumstances in oncology wherein a single-arm trial may be appropriate due to disease severity, unmet medical need, and concerns about the feasibility of an RCT.
We want to meet, know what is new, facilitate connections between organizations working in Biotech (e.g., Pharmaceutical R&D) and TechBio (e.g., AI for drug development). If you work in healthcare, be it as Researcher, Startup, VC, Entrepreneur, Digital, Developer, we want to network with you!
We want to meet, know what is new, facilitate connections between organizations working in Biotech (e.g., Pharmaceutical R&D) and TechBio (e.g., AI for drug development). If you work in healthcare, be it as Researcher, Startup, VC, Entrepreneur, Digital, Developer, we want to network with you!
Internationally, synthetic biology has already clearly established itself as a key technology of the future and a valuable industry, and in our country it is becoming increasingly clear that collaboration across all sectors is crucial to drive growth and innovation. To this end, the German Society of Synthetic Biology (GASB) is once again hosting its annual SynBio World Cafe.
The European Commission announced on 26 May 2021 the adoption of Regulation (EU) 2017/745, also known as the Medical Devices Regulation (MDR), entailing big changes for manufacturers, for whom bringing Medical Devices to the market is a challenging process.
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