Woodley BioReg is excited to announce our attendance at WHX Dubai 2026, taking place 9-12 February at the Dubai Exhibition Centre. Formerly Arab Health, WHX represents the evolution of this landmark healthcare event, uniting the entire global healthcare ecosystem under one name.
For over 50 years, Arab Health connected healthcare professionals worldwide. WHX now builds on that legacy with more content, more exhibitors, and more opportunities to connect, spanning every sector of healthcare. With representation from 180+ countries, WHX truly is where the world of healthcare meets.
As a trusted partner to the Biologics, Pharma, and MedTech industries, Woodley BioReg’s team of experienced consultants is ready to share technical knowledge and guidance across all stages of product development. We specialise in tailored compliance strategies in CMC, regulatory affairs, and quality assurance, supporting even the most complex projects.
We invite attendees to connect with us at WHX Dubai 2026. Whether you’re developing a new product, navigating regulatory challenges, or seeking guidance on quality compliance, our team is here to support your journey.
Will we see you there? To arrange a meeting in advance, please contact us. We look forward to connecting in Dubai and exploring opportunities to bring innovative, compliant, and patient-focused solutions to the global market.
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