Improve the market potential of your biomarker-based diagnostics and learn from our experts about:
Importance of pre-analytics in biomarker discovery, the advantages of biomarker validation and get insights on concrete use cases
Read More
The Interreg North-West Europe Codex4SMEs support programme offers a wide range of services to small and medium-sized enterprises (SMEs) in the life sciences and medical technology sectors working on the development of diagnostics.
The information event provides attendees with details about the application process for Codex4SMEs services, eligibility criteria for applicants, and the scope of services.
Read More
This session provides you with a practical approach to
laying the right foundation for your clinical trial. We help
you to understand the important links between the many
critical areas that will impact your trial. From design,
planning and through to trial execution, our experts will
discuss:
Read More
Improve the market potential of your biomarker-based diagnostics and learn from our experts about:
Importance of pre-analytics in biomarker discovery, the advantages of biomarker validation and get insights on concrete use cases
Read More
Are you a Pharma/Medtech/Companion Diagnostic SME or a company with Diagnostic products? Are you in need of IP strategy insights or do you have questions concerning patent protection and enforcement for your products?
Join our IP program NOW. The kick-off is free of charge.
Read More
Join the Meet & Match.Dx, a challenge-based acceleration programme that connects SMEs developing breakthrough diagnostic solutions with major pharmaceutical and medical technology companies in Europe through tailored workshops and one-to-one pitch sessions, with the aim to explore partnership opportunities.
Read More
There are significant changes in the European legislation applicable to IVDs. The IVDR (In Vitro Diagnostic Regulation) (EU 2017/746) has replaced the IVD Directive (98/79/EC) and will impose new requirements on Legal Manufacturers whose devices will be re-classified (devices higher than Class A) due to the rules associated with these changes.
Read More
There are significant changes in the European legislation applicable to IVDs. The IVDR (In Vitro Diagnostic Regulation) (EU 2017/746) has replaced the IVD Directive (98/79/EC) and will impose new requirements on Legal Manufacturers and other Economic Operators.
Read More
Med-Di-Dia (MDD) and Global Regulatory Services (GRS) are broadcasting a series of fireside chats throughout the week of 25th April – 29th April 2022, where our experts and resource partners shall talk and answer various questions around the IVD Regulations coming into effect from 26th May 2022!
Read More
The recent Corona pandemic taught us the importance of getting new diagnostics to market rapidly for keeping public life and the economy running. Join this online seminar to gain a clear overview of how to navigate from the development of your diagnostic, through intellectual property and financing issues, to market access. Meet our experts face-to-face to get tailored support for your diagnostic product.
This event is part of the Interreg NWE project Codex4SMEs which aims to support SMEs along the full diagnostics development value chain.
Read More
