arra.consulting is a Regulatory Consultancy Service providing regulatory expertise in the ever changing in vitro diagnostic medical device industry, offering a pragmatic approach to support start-ups, SMEs as well as larger manufacturers to successfully bring products to market by utilising experienced problem-solving skills and with being adept with adapting to changing requirements.


Regulatory Services to support the design, development, placement on market, distribution and post-market follow up activities for in vitro diagnostic medical devices to meet various markets.


Providing IVD Medical Device Regulatory support to projects by gaining an insight into understanding your business needs to deliver a pragmatic approach to bring to and maintain IVD medical device products on market.