Companies Forum

CRDN Companies Forum meetings welcome representatives from pharmaceutical, biotechnology and healthcare companies operating in the rare disease space who are interested in understanding the regulatory environment for orphan medicinal products and working collaboratively on projects.  Meetings are conducted under the Chatham House Rules and held  twice a year. Content for discussion is agreed amongst the group and high calibre speakers sourced by CRDN. Meetings are informative, relaxed and collaborative and members receive presented slides for future reference.

 

 an opportunity to network and collaborate 

Take a look at our previous meetings

In October 2017 our meeting involved a two-hour workshop designed to explore the process of achieving regulatory approval for an orphan medicinal product. This covered issues such as orphan designation and how to get it, scientific advice and protocol assistance, planning a clinical development programme when there are only a few patients across Europe, marketing authorisation and post-marketing surveillance. The meeting was chaired by Alastair Kent OBE, former Chair of CRDN and CEO of Genetic Alliance UK and the workshop led by Jordi LLinares, MD SSc, head of Scientific and Regulatory Management, Human Medicines Evaluation Division, European Medicines Agency.

A discursive workshop took place exploring the hill companies have to climb, and what help and support are available if they are to be successful in bringing an orphan drug to market. Providing an insight into the way that the Regulator approaches its task, and in so doing enabling companies to be better prepared when submitting an application for orphan designation and/or developing a clinical development plan intended to lead to a marketing authorisation.

In March 2018 we were joined by guest speaker Sheela Upadhyaya, Associate Director of the Highly Specialised Technology (HST) Programme at NICE. Sheela provided an overview of NICE’s work in relation to rare diseases and its HST programme, which is used to evaluate some medicines for rare disease patients. Within the Strategy, NICE is responsible for implementing the commitment to ‘ensure that there are appropriate procedures for evaluating the costs and benefits of treatments available for patients’. Medicines evaluated through the HST programme are for very small patient groups. HST evaluations seek to balance the potential value of a medicine with the uncertainties associated with its efficacy (as a result of data gathered from small populations). Sheela was joined by MHRA – Dr Daniel O’ Connor, Expert Medical Assessor, member of COMP and SAWP who provided a detailed presentation.

The summer 2018 meeting welcomed  guest speaker Dr Emma Harvey, E&RH Ltd  for an excellent presentation and discussion regarding Managed Access agreements in the UK, the perils and pitfalls with reference to the NICE HST process.  

For further information see the Companies Forum concept paper.

AUTUMN MEETING – 29 NOV 19 

Venue: Royal Society of Medicine, London 

Speakers: Prof Chas Bountra – University of Oxford, Dan Lewi – CATs Foundation, Tess Harris – PKD  UK, Allison Watson – Ring20

 

If we all got involved, imagine the difference we could make? Don’t just follow us, interact with us and join our thriving rare disease community! There’s lots of ways right here to begin your journey with us…

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