As the medicinal cannabis industry continues to rapidly evolve, Woodley BioReg stands steadfast in its commitment to lead the market in cannabis dried flower API cultivation compliance.
Our presence at Cannabis Europa 2024 is integral to our mission to lead the way in regulatory advice and guidance. Our goal is to offer invaluable insights and knowledge that will not only keep our clients informed but also place us at the heart of pivotal discussions fuelling the global expansion of the cannabis industry.
We streamline the process by managing all interactions with regulatory agencies for GMP licensure and HO certification, ensuring a smooth journey towards compliance. And our support doesn’t end here – we offer ongoing assistance in quality management and licence maintenance, empowering our clients to uphold the highest standards and regulatory compliance effortlessly.
We can also support on the development and registration of finished products and our overall work stretches far beyond advice and guidance.
We’re well-positioned to support with more ‘hands-on’ elements as required, and have the experience to add value through our existing working relationships with a number of EU medicinal cannabis clients.
And we are having more and more conversations as we seek to entrench our position as being at the forefront of expertise and industry exposure in this area.
Trust Woodley BioReg with your compliance journey; navigating complexity, elevating standards.
With our head office in the UK, EU base in Italy and satellite offices in the US and China — as well as partners in South Korea and Poland — we’re a truly global consultancy that understands the intricacies of the regulations across borders worldwide.
And as the only regulatory consultancy in the UK to hold a GMP licence, issued by the MHRA, we don’t just say we’re able help you do the same, we evidence it every day through our licence maintenance activities.
WBR has offices and partner groups in
But we also support clients working 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