From 11 to 14 November, Düsseldorf will once again welcome over 5,300 exhibitors and more than 83,000 visitors from nearly 70 countries, all gathered to explore the latest innovations in the medical industry.
As global experts in MedTech regulation and compliance, Woodley BioReg is looking forward to engaging with fellow professionals, sharing insights, and exploring cutting-edge developments in medical devices, drug delivery devices, and in vitro diagnostics (IVDs).
Our team of experienced consultants will be on hand to discuss how we can help businesses navigate the ever-changing regulatory landscape and ensure success in global markets.
MEDICA 2024 provides a unique opportunity to connect with industry leaders, specialists, and innovators across a wide range of sectors, from medical imaging and diagnostics to health IT and mobile health.
As the MedTech industry continues to evolve, we’re keen to discuss how Woodley BioReg can support your organisation in bringing products to market quickly, safely, and with full regulatory compliance.
We invite all attendees to connect with us during the event.
Whether you’re developing a new medical device or need guidance on regulatory compliance for existing products, we are here to help. Let’s meet at Medica 2024 and explore how we can work together to deliver innovative, compliant, and patient-focused solutions.
WBR has offices and partner groups in
They have provided an excellent level of focussed service and support to our regulatory and product conformance projects. Their services are competitively priced but uncompromising in their quality.
Associate Director, EU regulatory Affairs
Top 10 Pharmaceutical Company
Shown commitment and dedication over and above what you would sometimes expect from permanent members of staff, and is well respected by the people he has worked with and for.
Senior Manager, Regulatory Conformance
Top 10 Pharmaceutical Company
The effective way in which you took up the challenges of the assignment, together with your clear understanding of our business needs have played a key role in helping us achieve our targets.
AVP International Regulatory Affairs
Top 10 Pharmaceutical Company
Approached tasks with enthusiasm and worked extremely hard to pull together these submissions.
Through it all, have been diligent, highly responsive, proactive, communicative, and as a bonus, extremely good natured.
Associate Director, EU Regulatory Affairs
Top 10 Pharmaceutical Company
Excellent consultant with vast experience in both Regulatory and QA arenas: pragmatic scientist with high quality standards, he has resolved many issues.
Has been able to manage / coach personnel very efficiently. Finally, he knows the idiosyncrasy of the Company and the intricacies of products very well.
Successfully wrote module 3, submitted and approved with minimal request for further information.
Director, Regulatory Development
International Pharmaceutical Company