Portfolio Management Services

Before placing General Foods, Fortified Foods, Food Supplements, Food for Special Medical Purposes (FSMPs) or other Foods for Special Groups (including meal replacement products) on the market, regulatory due diligence must be performed to ensure compliance with applicable regulations in terms of composition and presentation to the final consumer. Additionally, some of the products will also require notifications to national authorities through various procedures.

The process of managing an entire portfolio from a regulatory perspective can be challenging, especially when products are intended for multiple markets. At JensonR+, our Portfolio Management Services is a solution to support manufacturers and brand owners, by removing your regulatory stress, allowing companies to focus on developing the best products.

The flexible approach of our Portfolio Management Services will support your company achieve compliance while working alongside your R&D and marketing departments to achieve their goals.

Our team and network of EU and International Regulatory Consultants will take on the regulatory burden, from initial launch projects and continuous maintenance of your products.

Medical Devices

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Formulation Lock-In

Working alongside your R&D department, regulatory due diligence will be performed on the proposed formulation to ensure the nature of ingredients and quantities are in line with applicable regulations, which includes the use of additives, nutritional ingredients, colours and flavourings.

Medical Devices

Label Development

Labelling compliance is an essential aspect of bringing new products to market and food labels must be given in a language that is understandable by consumers in the country in which you are selling your products. JensonR+ can provide adapted translations in English, all EU Languages and a growing number of international languages.

Medical Devices

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Product Notifications in all EU Countries

Most European countries have a notification system for food supplements and other regulated products (fortified foods, FSMPs etc.). Before it can be placed on the market, you must notify the national authorities by submitting various technical details about your product and a sample of the label. Notifications are made in the national language of each country.

Medical Devices

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Continuous Regulatory Support

After the expenditure of product development, it is essential to ensure that you optimise the return on your investment. At JensonR+ our expertise in global regulatory compliance alongside a well-sourced network of regulatory professionals, enables us to understand and develop the most effective strategy for your product, and support with further changes to labels and formulations or renotifications when required.

Our goal is to build long-term partnerships and be your trusted regulatory advisors.

Get in touch with us at business.development@jensongroup.com to find out how we can help.
Mihai Inceu
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