The food and nutrition industry in Europe continues to evolve under the demands of public health, market pressures, and regulatory reforms. Companies working in this space face scientific, operational, and compliance mandates that often require specialized consultants to address. Food safety legislation has become increasingly detailed over the last ten years, with greater consumer interest in clear labeling and the sourcing of raw materials leading to additional oversight. European regulators have increased controls on allergen declarations, nutritional claims, and manufacturing processes, putting steady pressure on producers, retailers, and suppliers alike to maintain proper documentation and traceability.Â
This has consequently placed consultancy groups in a better position, as organizations are demanding structured risk management and compliance planning to address these requirements.
According to food safety and regulatory monitoring data, allergen mislabeling and related documentation issues are among the leading causes of food recall notifications in Europe, with allergen and contamination concerns frequently dominating recall statistics in 2023. This is part of the greater challenge for companies seeking to operate within strict guidelines while also managing production schedules and distribution timelines. It is even more complex for organizations operating across borders, as even when countries follow shared European frameworks, regulations can vary by country. Many companies rely on external specialists who understand the relationship between manufacturing processes, verification systems, and regulatory controls to help them handle this.Â
Such specialists can help bridge the gap between operational practices and compliance expectations in a sector wherein accuracy is inextricably linked to public health and consumer trust.
It was against this backdrop that SIRE Life Sciences began developing its food and nutrition consultancy services in Europe, leveraging its broader experience in life sciences project support. Regulatory and operational advisory work under Stravers’ leadership focused on labeling compliance, food safety planning, and quality assurance for organizations seeking to align with European requirements. This is indicative of the company’s emphasis on structured methodologies and process transparency. The services encompass both short-term regulatory tasks and long-term system development, enabling clients to establish an internal framework that supports consistent compliance.
Labeling regulation is therefore at the heart of the company’s activity in this field. Food labeling in Europe requires detailed nutritional information, precise ingredient declarations, allergen alerts, and validated health-related claims. These regulations fall under a combination of EU food information legislation and national enforcement systems. SIRE Life Sciences supports companies in reviewing documentation to ensure that changes in formulation are correctly reflected in labeling, as well as in understanding the processes for verifying specific claims. Precise labeling is understood to be fundamental to compliance, while the firm’s services help its clients mitigate the risk of mislabeling that could lead to product recalls or sanctions.
The company also works extensively with HACCP planning, which remains a key preventive control system used in food production across Europe. This consists of hazard identification, critical control point monitoring, the validation of specific procedures, and detailed record-keeping for auditing purposes. With equipment updates, new suppliers, and entry into other markets, many food producers continually update their HACCP frameworks. SIRE Life Sciences helps organizations develop, review, or restructure this type of plan to mirror today’s manufacturing environments. This process fits well with the company’s broader consulting model, which focuses on the study of operations and system enhancements in regulated industries.
Other areas of work include product safety assessments and the operational steps necessary to maintain compliance throughout the production cycle. These assessments typically involve contamination risks, sanitation procedures, supplier verification, and end-product testing. Companies find added value in third-party input when establishing safety procedures that meet regulatory expectations and internal quality benchmarks. The role of the company is workflow examination, detection of possible chinks, and assistance for clients regarding how to be ready for inspections or certification reviews. This contributes to a consistent approach to safety governance that supports organizational reliability.
Innovation governance has also emerged as an essential component of food sector consulting, especially with the introduction of new products that feature plant-based ingredients, functional nutrients, or novel formulations. With new product development comes additional regulatory requirements, such as providing evidence for claims, conducting stability testing, and correctly documenting for approval pathways. SIRE Life Sciences works with clients to structure development processes so they meet regulatory expectations while enabling teams to advance product timelines. This support is designed to help companies balance creativity with compliance, a challenging combination in a competitive marketplace.
The integrated model weights regulatory knowledge and operational understanding equally in the company. Many clients have needs in several areas simultaneously, such as labeling updates for new formulations or safety assessments for revised manufacturing layouts. Integrated consulting allows organizations to maintain continuity across projects, reducing the risk of gaps in departments. This reflects broader industry trends, as companies increasingly seek consultants who support both regulatory and operational needs within a single engagement.
Companies offering food and nutrition in Europe are under the oversight of various authorities, including national food safety agencies, the European Commission, and standardization bodies that oversee certification and quality systems. In turn, compliance requires detailed record keeping, ongoing monitoring, and structured audit readiness. By supporting companies through these steps, SIRE Life Sciences develops more robust documentation practices and more predictable inspection outcomes. This is essential work in a sector where operational consistency is closely linked to regulatory performance.
Companies will always need consultancy groups that offer technical expertise, regulatory awareness, and operational insights as the food and nutrition sector continues to evolve. The work performed under Jordy Stravers’s guidance by SIRE Life Sciences reflects a steady evolution toward integrated support models that combine advisory services with broader process evaluation. The company’s role in labeling compliance, HACCP planning, product safety governance, and oversight of innovation demonstrates its commitment to helping organizations meet European regulatory requirements while managing day-to-day operational demands.







