REGULATORY SCIENCE IRELAND (RSI)

The ever-increasing complexity of health care products requires a data driven, evidence based approach to their regulation. Regulatory Science Ireland (RSI), a national response to these developments, is a network of interested parties from;

 

Academia | Regulatory Body (HPRA) | Pharmaceutical Industry | Medical Devices Industry | Government Agencies

 

RSI's Mission Statement

 

RSI’s mission is to unite stakeholders, including Academia, Pharmaceutical and Medtech industries, the Regulator and Government agencies, in the pursuit of an

 

integrated Irish response to global Regulatory Science initiatives that are beneficial to the patient.

 

 

 

RSI will fulfil its mission through facilitation of relevant research, training and communication, thereby creating an environment that:

 

  • Facilitates Irish contributions to an effective response to the increasing complexity of Health Care Products and their associated Regulatory Systems;
  • Creates a cohort of Irish based Regulatory Science experts
  • Further strengthens the value proposition of Ireland as an attractive location for Health Care Product related activities

RSI NEWS FEED:

 

 

 

RSI will be participating in the European Commission  multi-stakeholder workshop on biosimilar medicines. This event will be held on 5 May in Brussels.  Report from last years event is below

 

http://ec.europa.eu/growth/tools-databases/newsroom/cf/itemdetail.cfm?item_id=8968

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

How RSI is Organised

 

RSI is committed to the development of an integrated Irish response to the global Regulatory Science effort by establishing an environment through which relevant research, training and communication creates a cohort of Irish based Regulatory Science experts and further strengthens the value proposition of Ireland as an attractive location for Health Care Products.

 

How RSI Works

 

The RSI Board Of Directors creates an annual work plan in the following three areas.

Academia

 

Regulatory Body (HPRA)

Pharmaceutical Industry

Medical Devices Industry

Government Agencies