NATURAL · HEALTH · FUTURE
From formulation and sampling to manufacturing, packaging and export support, NUSVIVA helps wellness brands bring functional nutrition products to market.
Manufacturing solutions across China, Germany and Malaysia for international B2B partners.
Gummies · Capsules · Softgels · Powders · Tablets · Oral Films · Liquids · Functional Foods
Format imagery is illustrative; availability, specifications and production scope are confirmed for each project.
Eight format directions · inquiry-led
Explore NUSVIVA
Explore manufacturing, dosage forms, OEM/ODM development and quality support.
Global manufacturing
Connect product development with the manufacturing route, facility and supply plan that fit the brief.
Product formats
Compare gummies, capsules, softgels, liquids, tablets, powders and oral films for your product brief.
OEM / ODM development
Move from formulation and sampling to packaging prototypes built around your brand and target market.
Global regulation and quality
Review product quality, documentation and destination-market requirements in context.
MANUFACTURING IN MOTION
A short look at the production environment, dosage-form capabilities and working context behind selected project routes.
CUSTOM PRODUCT DEVELOPMENT
Shape your concept through formulation, sampling, packaging, quality review and manufacturing.
From your first idea to a finished product, our team supports every step of the development process.
QUALITY & LABORATORY CAPABILITY
Quality control starts long before production.
NUSVIVA integrates laboratory testing, raw material evaluation, formulation review and production quality control throughout the product development process.
Applicable test methods, documents, facility scope and destination-market requirements are confirmed for each project.
Explore Our Quality System →
START YOUR OEM / ODM PROJECT
Share your market, product concept and dosage form so formulation, packaging and route options can be reviewed.
Develop the formula, dosage form, packaging and presentation around your brand.
HOW IT WORKS
A clear and integrated OEM/ODM process from product concept and formulation to manufacturing, compliance and global delivery.
Share your target market, product concept, dosage form, specifications and estimated quantity.
YOUR NEEDS
Our R&D team develops or optimizes the formula based on your product requirements and target market.
TAILORED SOLUTIONS
Confirm the formula, flavor, appearance, dosage form and packaging direction before mass production.
SAMPLE APPROVAL
Review ingredients, formula, labeling and required documentation for the target market.
COMPLIANCE SUPPORT
Raw material control, manufacturing, testing and finished-product inspection are coordinated for the approved project scope.
RELIABLE MANUFACTURING
Complete final packaging and support international logistics and market delivery.
TO GLOBAL MARKETS
FREQUENTLY ASKED QUESTIONS
Our manufacturing network works with facilities holding relevant quality and food-safety certifications, which may include GMP, HACCP, ISO, NSF，CNAS，Halal and other applicable certifications. The exact certification scope depends on the manufacturing site, product category and project requirements.
MOQ varies by dosage form, formula, packaging and manufacturing location. Share your product requirements with us, and our team will confirm the applicable MOQ for your project.
Yes. We support custom formulation, formula optimization and new product development based on your concept, target market, dosage form and positioning.
Yes. If you already have a formula or product specification, our team can review it for manufacturing feasibility, ingredient sourcing, dosage form and production requirements.
Yes. Samples can be arranged for formula, flavor, appearance and product evaluation before moving into commercial production.
We support powders, tablets, capsules, softgels, gummies, liquids, oral films and other customized formats, depending on the selected manufacturing route and project requirements.
Yes. We support private-label and customized packaging solutions, including bottles, jars, sachets, stick packs, pouches and cartons.
Lead times depend on the formula, dosage form, packaging and level of customization. After reviewing your project, our team will provide an estimated sampling and production timeline.
Yes. Our team can review formulas, ingredients, labels and supporting documents based on your target market and project requirements. Specific regulatory requirements are confirmed according to the destination market.
Our manufacturing and product development network includes capabilities in China, Malaysia and Germany. The recommended manufacturing route depends on product format, market requirements, certification needs, quantity and brand positioning.
Typical response within 48 hours
DOCUMENTATION FRAMEWORK
Project documentation may include quality-management, food-safety, laboratory, market-entry and batch records. Availability and applicability are confirmed for the responsible facility and agreed project scope.
Relevant management-system and food-safety documents are reviewed for the selected facility and project scope.
Testing methods, laboratory documents and applicable result scope are checked for the specific product and project.
Required documents are assessed against the destination market, product category and selected manufacturing route.
Applicable production, testing, release and supply records are confirmed according to agreed project requirements.
Any named standard, certificate, registration or laboratory recognition is checked against the responsible legal entity, facility, covered scope, validity period and permitted public use before publication.
CONTACT NUSVIVA
Share your market, product type, dosage form and estimated quantity so we can review the next step.
