Your oral film project, from brief to batch
An agreed development scope, realistic loading targets, controlled sampling and manufacturing handovers.
A formula shaped around your brief
Start with ingredient identity, target strength and the destination market. Assess film loading, taste and stability before locking specifications.
Packaging that protects the film
Pair the film with an individually sealed barrier sachet and a retail structure designed for your channel.
Sample first. Confirm the specification.
Use prototype feedback, analytical checks and packaging proof approval to turn an idea into a controlled project.
A documented manufacturing workflow
Agree on formulation, quality attributes, batch documentation and responsibility at each handover.
Your brand, with clear project terms
Discuss minimum order quantity, sample scope, artwork, production timing and export coordination before committing.
Custom oral film development, from brief to batch
- Which service model fits our project?
- What is the development workflow?
- What are the caffeine sample and order terms?
OEM
Develop and manufacture against an agreed customer-owned specification.
ODM
Configure a concept around your ingredients, flavor, market and brand.
CRO
Investigate a defined formulation, compatibility or analytical question.
CDMO
Connect development, process transfer and commercial manufacturing.
All oral film types in this website can be discussed under OEM, ODM, CRO or CDMO models. A service label does not establish that every active ingredient, payload or market route is feasible. We define the actual technical and commercial scope before the project starts.
Eight stages, with agreed decision points
Project brief
Define intended market, adult target audience, ingredients, strength, flavor, packaging and commercial objectives.
Formula feasibility
Assess film loading, compatibility, sensory requirements, ingredient status and the analytical plan.
Prototype sample
Prepare agreed prototypes and capture feedback against a written brief.
Stability & performance review
Agree and conduct the necessary physical, analytical, microbiological and packaging assessments.
Specification lock
Approve formula, film dimensions, acceptance criteria, labeling responsibilities and release documents.
Packaging proof
Approve sachet barrier, dielines, print proofs, carton structure and count.
Production & quality checks
Manage controlled manufacture, in-process inspection, batch identification and agreed release testing.
Export coordination
Confirm trade terms, shipping route, documents and handover responsibilities.
View the detailed 10-action customization workflow
- Gather requirements
- Targeted R&D
- Sample testing
- Finalize sample
- Tailored design
- Approve design
- Sign contract
- Box prototyping
- Approve prototype
- Start production
Adapted from the company-supplied customization process. View the source artwork.
Reference commercial terms for the caffeine project
| Reference formula | 40 mg caffeine + 40 mg L-theanine + 2.4 mcg vitamin B12 per film |
|---|---|
| Minimum order per flavor | 2,000 boxes, 30 films per box; 60,000 films total |
| Sample development fee | USD 200 per SKU; creditable against a later commercial order under agreed terms |
| Sample preparation | 7 working days under the agreed sample brief |
| Commercial production | Approximately 3 weeks after formula and packaging-design approval |
| Custom branding | Printed individual sachets and retail cartons |
| Additional costs | Freight, external testing, certification, registration and other third-party work as quoted |
What the initial brief should include
- Destination country and product classification you intend to investigate.
- Ingredient identity, target amount per film and proposed serving.
- Adult target audience for caffeine concepts; separate life-stage suitability for other briefs.
- Flavor, color, sweetener restrictions and vegan or Halal requirements.
- Film dimensions, number of sachets per carton and retail format.
- Target quantity, launch date, analytical requirements and documentation needs.
Answers for your next project
Clear starting points for formulation, commercial terms and market review.
Do you have the technology and facilities to manufacture oral dissolving films?
Yes. We have oral dissolving film technology and manufacturing facilities. A project starts with the formula, film format, intended market and quality requirements so the correct development and production route can be confirmed.
Can you develop a custom formula?
Yes. We accept OEM and ODM briefs and can support CRO and CDMO development projects. Ingredient selection, strength, film loading, taste, stability and destination-market eligibility are reviewed before a final formula is agreed.
What is the minimum order quantity per flavor?
For the caffeine oral film reference project, the minimum order is 2,000 boxes per flavor, with 30 films per box, equivalent to 60,000 films. Different formulas, counts and packaging structures require a project-specific quotation.
Can you provide samples, and what do they cost?
Yes. Sample development for the caffeine reference project costs USD 200 per SKU. The fee can be credited against a later commercial order. The sample scope, number of iterations, shipping and credit conditions are confirmed in the quotation.
Can you support Halal certification and vegan formulations?
Our factory has Halal certification, and vegan formulations can be customized on request. The applicable manufacturing site, certificate scope and validity are checked for the project. Every ingredient, flavor, processing aid and packaging claim must be reviewed before a finished product uses either claim.
Can you customize individual sachets and retail boxes?
Yes. We support custom-printed branded individual sachets and retail cartons. Confirm the film size, moisture barrier, pack count, dielines, artwork and proof samples before production.
Can you help with import and dietary supplement documentation?
We can assist with available quality documents and regulatory coordination for the destination market. Any third-party testing, registration, certification or other chargeable work is paid by the customer. Assistance does not establish that a formula is approved or legally marketable in every country.
What are the sample and production lead times?
For the caffeine reference project, sample preparation is 7 working days. Commercial production is approximately 3 weeks after the formula and packaging design are approved. These are planning terms, subject to raw-material availability, approvals, testing scope and order confirmation; shipping time is additional.