Based in the UK, IPCons was founded in 2005 and has grown steadily into a strong and trusted drug registration consultancy to the pharmaceutical, healthcare and biomedical sectors. We have provided regulatory affairs consulting and support to companies including Pfizer, Novartis and Abbott Laboratories. Our clients are located throughout Europe, US and the rest of the world.
Delivering Project Management
Regulatory strategy and project management is our main focus, providing individually tailored and flexible services, with no limit to project size. The services we offer are made available through our highly professional and experienced core team and when a project requires it our ability to scale-up through access to a body of over 130 experienced regulatory consultants who are all endorsed and reviewed within this peer group.
With skills in all aspects of the product life cycles of (bio)pharmaceuticals and medical devices, IPCons can offer expertise from concept to market of your products.
We also pioneered Patient Information Leaflet (PIL) design and User Testing through our PIL2005 company (now part of IPCons), enabling us to assist companies of all sizes in meeting with Package Leaflet design and readability testing requirements.
To learn more about exact services IPCons provides please follow the relevant links or contact us directly.