At NATUREPROF, we believe that sustainable beauty and health begin with "thoroughly researched nature." Therefore, every formula is developed transparently, ethically, and with the user and the environment as our top priorities. This includes everything from ingredient selection and formula design to testing, production, and verifiable documentation.
OUR SERVICES
Work process
Gather product concept information based on customer needs, covering both product and marketing information. For example, what type of product do customers want? What will it be used for? Who is the target audience? What form does the product prefer? What is the price range? What is the overall appearance, label, and packaging like? What are the product's unique selling points?
- Design formulas based on brand requirements, including ingredient options/formula concepts suitable for practical use.
- Prepare samples for testing, adjusting texture, scent, color, stability, and user experience.
- Plan necessary testing such as stability, compatibility, and safety according to product type.
- Prepare samples for testing, adjusting texture, scent, color, stability, and user experience.
- Plan necessary testing such as stability, compatibility, and safety according to product type.
- Assess product types and registration/notification procedures with relevant agencies (FDA).
- Review labeling to ensure compliance with regulations and reduce the risk of misleading communication.
- Prepare necessary supporting documents, such as formula information, product details, and other accompanying documents.
- Review labeling to ensure compliance with regulations and reduce the risk of misleading communication.
- Prepare necessary supporting documents, such as formula information, product details, and other accompanying documents.
- Summarize the scope of work and terms and conditions jointly: Minimum Order Quantity (MOQ), lead time, payment terms, and work plan.
- Establish joint quality standards: product specifications, acceptance criteria, and quality control/quality assurance (QC/QA) plans.
- Establish necessary agreements, such as confidentiality, intellectual property scope, and requirements for formula/work changes.
- Establish joint quality standards: product specifications, acceptance criteria, and quality control/quality assurance (QC/QA) plans.
- Establish necessary agreements, such as confidentiality, intellectual property scope, and requirements for formula/work changes.
- Ensure the label layout is complete and accurate: product name, instructions for use, warnings, ingredients, relevant registration numbers, and manufacturer/distributor information.
- Assist in developing label communication guidelines that comply with regulations and reflect the brand image.
- Review artwork files before production to ensure they are ready for printing/packaging.
- Assist in developing label communication guidelines that comply with regulations and reflect the brand image.
- Review artwork files before production to ensure they are ready for printing/packaging.
- Inspect incoming raw materials and packaging: documentation, source, product condition, and compliance with specifications.
- Implement a “receiving-quarantine-release” system according to quality procedures to ensure compliance before production begins.
- Reduce the risk of on-site problems such as incorrect material models, wrong labels, mismatched sizes, or inconsistent quality.
- Implement a “receiving-quarantine-release” system according to quality procedures to ensure compliance before production begins.
- Reduce the risk of on-site problems such as incorrect material models, wrong labels, mismatched sizes, or inconsistent quality.
- Produced according to specified formulas and manufacturing methods. Process controls are implemented at critical points to ensure consistent quality.
- In-process testing is performed to check viscosity, color, odor, and specific product parameters.
- Production records are maintained at every stage to facilitate traceability and support repeat production.
- In-process testing is performed to check viscosity, color, odor, and specific product parameters.
- Production records are maintained at every stage to facilitate traceability and support repeat production.
- Conduct quality checks according to the agreed-upon plan, including physical, chemical, and microbiological aspects (as appropriate for the product).
- Verify the accuracy of documents and processes to ensure compliance with established standards.
- Issue a batch quality confirmation document (e.g., COA) and summarize the results for customer acceptance.
- Verify the accuracy of documents and processes to ensure compliance with established standards.
- Issue a batch quality confirmation document (e.g., COA) and summarize the results for customer acceptance.
- Pack into containers, seal, label, and assemble secondary packaging according to the approved design.
- Print the lot number/production date/expiration date correctly and clearly.
- Check for completeness before delivery, such as tightness, cleanliness, and accuracy of labels/boxes.
- Print the lot number/production date/expiration date correctly and clearly.
- Check for completeness before delivery, such as tightness, cleanliness, and accuracy of labels/boxes.
- Arrange delivery according to agreed terms, along with necessary supporting documents.
- Provide recommendations on appropriate storage and transportation to maintain product quality.
- Post-delivery support: assisting with repeat production, upgrading subsequent batches, and future product line expansion.
- Provide recommendations on appropriate storage and transportation to maintain product quality.
- Post-delivery support: assisting with repeat production, upgrading subsequent batches, and future product line expansion.