Quicker to Market
Avoid costly delays in getting your product to market.
Full lifecycle project management.
Trusted & Proven
Delivering success for Fortune 500 companies.
Helping to ensure your projects meet full regulatory compliance.
Regulatory Affairs Consulting
We are experts in
Regulatory Affairs and Drug registration
With over 15 years of delivering candidate to market drug registration and project management of regulatory affairs projects to the pharmaceutical, biomedical and healthcare sectors. Your project is safe in our handsSTART THE CONVERSATION
A few things we’re great at
Our expertise lies in our ability to determine the regulatory strategy you need to deliver fast, efficient and cost effective results regardless of project size.
Guiding clients through the process of developing successful regulatory strategies and then helping them to deliver these is our core service. We also assist with scientific advice, orphan and paediatric plans and clinical trial and marketing authorisations.
Vital services including the writing and maintenance of dossier and technical files, production of regulatory intelligence reports, package leaflet design and readability testing are all within our core competencies.
Regulatory Compliance & Training
Assistance with in-house regulatory training and services geared towards compliance, including technical writing, inspection support and SOP audits and writing is something we are proud to say we can support you with.
Determine regulatory market opportunities, timelines, costs and hurdles for global project.
All global markets where registrations did not currently exist were in scope.
Timely presentation to Snr Leadership of all opportunities to enable decision to proceed.
Approval to proceed granted for major global growth project prior to formation of NewCo. formation.
Don’t take our word for it – here’s what our clients say:
Working with Nik and the rest of the team at IPCons was a pleasure and they delivered on all our agreed goals for this complex project.
IPCons worked closely with our Medical Writing teams to effectively lead key submission projects that required multi-functional team input.
I had the pleasure of working with Nik on a global pharma company’s project requiring regulatory skill, commitment and dedication. He was remarkable in meeting the clients requests and going that extra mile to provide a high quality of work and attention to detail. It would be an honour to work with Nik again.
Woodley Bio Reg
Three reasons why IPCons are your preferred pharmaceutical consultancy partner
Our Core Team
Success comes from the top down, meet the board
CEO and Founding Director
CFO and Company Secretary
It is important to be aware of the current changes affecting the regulatory world we are all working in.
Making contact is the first step towards success for your project