Kick-start your Novel Food Application with us

May 07, 2021

Submitting a Novel Food application can be demanding, especially when you consider the time and expense involved in the task. We’d like to help by giving you the option of a smoother process with the assistance of our three step approach where we take care of the application process for you from start to finish, with flexible solutions to suit your business needs and budget.

Our expertise in regulatory and scientific affairs comes from years of engagement with regulatory authorities and a highly skilled team from a diverse scientific backgrounds, meaning we ensure that all required areas of your Novel Food application are covered in order to be authorised by the Food Standards Agency (FSA) / European Food Standards Agency (EFSA). The journey to a market-ready product has never been easier!

Our 3 step Novel Food process

We keep things simple, with our three step approach covering everything required for a successful Novel Foods submission.

The process includes:

Step 1 – Information/Product Review
Step 2 – Collation of Technical and Scientific data
Step 3 – Submission to Regulatory Authority

How to start your Novel Food application

Commence this process with Step 1, to help you determine where you are currently in the process of getting your Novel Food product authorised and what is needed for your application to be successful (extra data required, cost and timeline) – with no obligation to complete the full application with us.

At the end of this step, we will have carried out the following process;

Data Analysis – Performed a thorough review of the data held by you, in regards to the product you wish to submit for authorisation.
Strategy Development – Compared the data held by you to the regulatory requirements, created a strategy document to gather all of the technical and scientific data for a successful submission. Strategic questions will then have been drafted to address any remaining uncertainties in the formulated strategy.
Project Plan – Created a bespoke project plan for addressing the regulatory requirements along with an estimated timeline.

This information will provide you with the essential data needed to move forward with your application and get you one step closer to getting your product on the market!

Our first-class service

There are many advantages to working with us, including;

Cost Reduction – specialising in both regulation and compliance, our expert approach to compliance is pragmatic and risk-based, reducing overall project costs.
Time saving qualities – your work is overseen by your dedicated project manager.
Agility – we know that one solution doesn’t fit every company.
Simplicity – we manage all requirements from start to finish.
Accurate communication – laboratory and regulatory teams are able to liaise to ensure no misalignment of expectations or requirements.
Valued confidentiality – we maintain client information in utmost confidence, with extensive procedures to protect data from loss or theft.
Geographical coverage – we have offices in the EU, UK & USA.