Running 27-30th January at the Dubai World Trade Centre, this landmark 50th-anniversary edition is set to bring together over 3,800 exhibitors and more than 60,000 healthcare professionals from 180 countries.
As a leading provider of trusted advice and guidance to the Biologics, Pharma and MedTech industries, Woodley BioReg is eager to engage with industry leaders, innovators, and professionals at Arab Health.
Our team of seasoned consultants, each with extensive industry or agency experience, is dedicated to delivering top-tier technical knowledge across all stages of product development.
We specialise in crafting tailored compliance strategies in CMC, regulatory affairs and quality assurance, ensuring the success of even the most complex and niche projects.
Arab Health 2025 offers a unique platform to explore the latest advancements in medicines, medical equipment, devices, diagnostics, and healthcare technologies.
With the event’s focus on ‘Connecting Minds, Transforming Healthcare’, we are particularly interested in engaging with the innovative features on the show floor, such as the Transformation Zone and the Smart Hospital and Interoperability Zone.
These innovative ideas align with our commitment to staying at the forefront of healthcare technology and regulatory excellence.
We invite fellow attendees to connect with us at the event.
Whether you’re developing a new product, navigating regulatory challenges or seeking expert guidance on quality compliance, our team is here to support your journey.
Let’s meet at Arab Health 2025 to discuss how we can collaborate to bring innovative, compliant, and patient-centric solutions to the global market.
To arrange a meeting with our team, please contact us in advance.
We look forward to connecting with you in Dubai!
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