Concept to launch
Design, trials and scale-up planned as one programme.
Research & Development Services
BEMCON reviews product labels against requirements applicable to the product category and intended market. Reviews cover label content, consistency with the actual formulation and supporting evidence for nutritional or marketing statements.

BUILT AROUND YOUR REQUIREMENT
Each engagement starts with the required outcome, operating context and evidence of success. The result is a focused Product Labelling & Regulatory Conformity scope with clear responsibilities and handover points.
Design, trials and scale-up planned as one programme.
Evidence that products and processes perform as intended.
Registration dossiers for SFDA, GSO and other authorities.
Sensory panels, customer studies and surveys.
8 SPECIALIST CAPABILITIES
Select the capabilities that match your Product Labelling & Regulatory Conformity requirement, operating context and agreed delivery stage.
Review proposed labels against the requirements identified for the product and destination market. Provide an issue register distinguishing missing information, inconsistent wording and items requiring clarification.
Compare product names and ingredient declarations with the formulation and ingredient specifications. Identify omissions, inconsistent terminology and differences between technical records and the proposed artwork.
Review allergen declarations against formulation details and available ingredient documentation. Highlight inconsistent statements and information gaps requiring clarification with suppliers or the manufacturer.
Check nutrition information against the supporting calculations or analytical reports supplied for the product. Review consistency of declared values, units, serving information and proposed presentation.
Examine nutritional and marketing claims against the evidence provided and applicable review criteria. Identify unsupported statements, missing substantiation and wording requiring revision before publication.
Review date marking, batch identification, storage conditions and use instructions against the product’s technical documentation. Check consistency with available shelf-life findings and intended handling conditions.
Review applicable declarations such as net quantity, origin and required language content. Identify missing details and inconsistencies between language versions, product documents and packaging artwork.
Provide marked-up artwork and a consolidated correction list for the design team. Recheck revised versions against identified issues and record any unresolved matters before printing.
HOW WE WORK
A defined workflow keeps the work aligned with the approved scope and makes progress, decisions and handover easier to manage.
Scope your requirementConfirm the purpose, operating context, stakeholders and expected outcome for Product Labelling & Regulatory Conformity.
Define activities, responsibilities, inputs, dependencies, checks and approval points.
Complete the specialist work while keeping progress, risks and decisions visible.
Confirm the completed scope, record outcomes and agree practical next actions.
WHAT YOU RECEIVE
Documented objectives, responsibilities, constraints, assumptions and acceptance points.
Relevant analysis, coordination and technical work for Product Labelling & Regulatory Conformity.
Findings, decisions, completed checks and limitations recorded for the agreed scope.
Prioritised actions for implementation, follow-up, improvement or ongoing support.
GET IN TOUCH
Choose the type of request and share the details. The right BEMCON team will respond.