Fabricación de suplementos
Fabricación de suplementos de marca blanca
Develop capsules, gummies, powders, tablets, softgels and liquid supplements through custom formulation, sampling, private label packaging and commercial production. We support brands, distributors and importers with OEM/ODM manufacturing and project documentation.
Purchasing Basis
Compare the Manufacturing Brief by Dosage Form
These are selection and approval criteria, not promised equipment ranges or fixed production specifications.
- Cápsulas
- Separate active serving from fill weight; agree shell, size and count, plus applicable fill and closure checks.
- Tablets
- Specify active serving, total tablet weight, tooling and coating; agree applicable compression and finished-tablet checks.
- Cápsulas blandas
- Define oil or suspension composition, measured active contribution, fill weight and shell compatibility; agree leakage and stability checks.
- Gominolas
- Separate active per serving from piece weight and count; review base, sensory targets, stability and pack protection.
- Powders
- State kilograms for bulk or units and serving weight for retail; agree blend checks and a reproducible preparation method.
- Liquids & drops
- Specify concentration per mL, serving volume, carrier and measured-dose component; agree relevant microbial, physical and pack checks.
Manufacturing Capabilities
Manufacturing Capabilities by Dosage Form
Each dosage form requires a different formulation, process, packaging and quality approach. Explore the manufacturing route that matches your product brief.
Fabricación de cápsulas
Capsule projects reviewed around fill weight, shell selection, blend flow and commercial packaging.
Ver la fabricación de cápsulas
Fabricación de gominolas
Gummy development aligned around active load, flavor, texture, shape and production requirements.
Ver la fabricación de gominolas
Fabricación de polvo
Powder projects reviewed around ingredient load, blending, flavor systems, flowability and filling.
View Powder Manufacturing
Fabricación de tabletas
Tablet production planned around compression, tablet weight, coating and packaging format.
View Tablet Manufacturing
Fabricación de cápsulas blandas
Softgel projects developed around liquid fill, shell compatibility, encapsulation and stability.
View Softgel Manufacturing
Fabricación de líquidos
Liquid projects reviewed around solubility, carrier system, dose delivery and controlled filling.
View Liquid Manufacturing
Inside the Facility
See the Manufacturing Process Behind Your Product
Review production, filling, inspection and quality-control environments used across different supplement manufacturing projects.
Selected facility images show real production, filling and packaging environments. Exact equipment and manufacturing routes vary by dosage form and project.
Commercial Project Workflow
Desde la ficha técnica del producto hasta la producción comercial
Every commercial supplement project follows a clear path from product definition and sample approval to packaging, production and shipment planning.
Ficha del producto
Define the formula target, dosage form, serving size, target market, packaging direction and commercial quantity.
Formulation & Sample Approval
Review feasibility, refine sensory and technical requirements, and confirm the approved sample before scale-up.
Embalaje y documentación
Confirm packaging format, artwork scope, specifications, testing requirements and supporting project documents.
Commercial Production & Shipment
Finalize MOQ, production schedule, batch review, packing and shipment planning.
Envases de marca propia
Packaging Support Built Around the Product Format
Coordinate primary packaging, serving count, artwork scope and secondary packaging around the dosage form, target market and commercial order plan.
Botellas
Bottle counts and label formats for capsules, tablets, gummies, softgels and liquids.
Bolsas verticales
Flexible multi-serve packaging for powders, gummies and other suitable products.
Sobres y envases tipo stick
Measured single-serve formats for powders and liquid supplement applications.
Blísteres
Unit-dose presentation for tablets, capsules and softgels where project requirements allow.
Cajas de cartón
Secondary packaging for branded presentation, product protection and retail-ready projects.
Certifications & Compliance
Certifications & Quality Documentation
Review current facility and product-scope certifications alongside specifications, batch COAs, testing records and supporting project documents. Availability varies by product, facility and destination market.
Quality Control
Quality Control at Every Production Stage
Each project is reviewed against approved specifications from incoming materials through in-process checks, finished-product review and batch documentation.
Incoming Material Review
Verify material identity, specifications and applicable incoming documentation.
In-Process Control
Monitor process parameters and manufacturing checks relevant to the dosage form.
Finished Product Review
Review appearance, packaging configuration and applicable testing before release.
Batch Documentation
Compile batch COAs, specifications and supporting project files for commercial review.
Client Project Feedback
What Different B2B Buyers Value During a Manufacturing Project
We started with a product concept rather than a finished formula. The sample stage helped us narrow the serving format and packaging before committing to the first commercial run.
The project began from an existing specification. What helped most was having sampling, packaging updates and documentation reviewed together instead of treating them as separate steps.
For our sourcing work, documentation and consistency matter as much as the product itself. Reviewing specifications, batch files and packaging requirements in one project workflow made the process easier to manage.
Manufacturing FAQ
Preguntas frecuentes sobre la fabricación de suplementos
What supplement dosage forms can you manufacture?
Manufacturing capabilities include capsules, gummies, powders, tablets, softgels and liquid supplements. The exact production route, MOQ and development requirements depend on the formula, dosage form and packaging plan.
What should be agreed before a manufacturing route is selected?
Provide ingredient identities and active amounts per serving, intended audience and country, dosage form, pack and expected units. Identify which formula, sample, test methods and release documents need approval. The manufacturing page describes project routes; actual ingredient eligibility, equipment fit and commercial scope are confirmed for the proposed product.
What is the MOQ for private label supplement manufacturing?
MOQ varies by dosage form, formula, packaging format and production setup. Share the target product, pack configuration and quantity so the appropriate commercial route can be reviewed.
Can I request samples before commercial production?
Sampling is available for project review before commercial production. Sample scope and timing depend on the dosage form, formula, flavor or appearance requirements and any custom tooling involved.
Can you provide private label packaging?
Packaging can be coordinated around bottles, pouches, jars, sachets, stick packs, blisters, cartons and other project-specific formats where applicable.
What quality documents are available for B2B projects?
Applicable documents may include specifications, batch COAs, testing records, allergen information, packaging files and current certification documents. Availability and certification scope vary by product and manufacturing facility.
How long does supplement development and production take?
Timing depends on formulation, sample approval, packaging preparation, testing, tooling and commercial quantity. A project-specific schedule can be reviewed once the product brief and target launch requirements are confirmed.
Consulta sobre la fabricación de suplementos
¿Estás listo para desarrollar tu suplemento?
Share your dosage form, formula or product concept, packaging format, target market and expected quantity. Our team will review feasibility, sampling, documentation and commercial production requirements.