01 · Packaging
Packaging Pilot
For teams with a formula or current package that need format, fill-volume, MOQ and pack-out direction.
Controlled two-site BFS manufacturing
Launch small-dose skincare with less packaging guesswork.
Steridose Labs delivers serum sample packaging, BFS filling, trial-kit pack-out and supplier qualification through a controlled two-site manufacturing network for overseas beauty, sourcing and R&D teams.
21
BFS blow-fill-seal lines across two factory sites
0.5–20ml
Core format review range
10,000+
Standard commercial pilot
NDA
Before formula transfer
Product system
Four format families. One clearer decision.
Start with how the product will be sampled, carried and used. Manufacturing terminology comes after the project need is clear.
010.5ml–20ml format familyBFS single-dose ampoulesLDPE ampoules for serum, essence, booster and other small-dose liquid programs.02Sampling and secondary packTrial kits and GWP samplesFormat and pack-out planning for launch trials, discovery sets and campaign sampling.03Portable single-use routinesTravel and professional routinesCompact take-home formats for travel, clinic, spa and professional skincare programs.04Alternative application formatLiquid-filled applicatorsPre-filled swab routes for topical liquid sampling and controlled application.
Three ways to begin
Enter at the stage your project is actually in.
A finished formula, an early concept and a complete market-test kit do not need the same first conversation.
02 · Development
Formula + BFS Concept Sample
For teams that need formula direction, NDA transfer or filling-fit review before commercial packaging.
03 · Market test
Turnkey Market Test Kit
For private-label, distributor and turnkey partners testing a complete sample program before scale-up.
Controlled manufacturing network
One accountable team. Two controlled production sites.
Steridose Labs is the international commercial and technical team for a controlled two-site BFS manufacturing network. The network has 21 BFS blow-fill-seal lines across two factory sites. Each qualified project stays within one Steridose-led workflow while the better-fit production site is selected by formula, format, document scope, quantity and schedule. Capacity only matters when the format, formula, evidence needs and schedule can be qualified together.
Production path 01
BFS Specialist Facility
Format-focused BFS production for qualified single-dose liquid projects.
- Best fit
- Ampoule format, mould, filling range and scale review
- Confirm before site selection
- Formula fit, line scope, quality records and schedule
Production path 02
Integrated R&D + Manufacturing Facility
Formula, laboratory and broader OEM/ODM support alongside BFS manufacturing.
- Best fit
- Development support, formula adaptation and broader pack-out needs
- Confirm before site selection
- R&D scope, production route, document scope and timing
Production-site selection
One Steridose brief stays within the controlled network while the better-fit production site is selected.
Commercial entry
10,000+ units is the standard commercial pilot path, with selective 5,000-unit review.
Formula confidentiality
NDA alignment can take place before proprietary formula details are transferred.
Evidence access
Facility identity, certificate scope and applicable documents are shared with qualified projects at the appropriate review stage.
From brief to scale
A four-step path with fewer hidden assumptions.
Each stage removes a different risk before production planning becomes expensive.
01
Define the launch
Share the use case, formula status, target market, format and timing.
02
Confirm technical fit
Review fill volume, material route, formula handling, pack-out and document needs.
03
Build the pilot scope
Align samples, approval files, MOQ, lead-time variables and commercial assumptions.
04
Prepare for scale
Use pilot feedback to plan reorders, channel expansion and the next production stage.
Decision examples
See how similar launch projects are scoped.
Procurement resources
Documents your sourcing and quality teams can review.
What teams usually confirm before formula transfer.
Can Steridose support custom skincare sample packaging?
Custom review can include BFS LDPE ampoules, liquid-filled swabs, trial kits, labels, pouches, cartons, inserts, pack-out and NDA formula-transfer needs.
What makes an RFQ quote-ready?
Include the target format, liquid type, fill volume, current package, pilot quantity, market, timeline, quality-document needs and NDA status.
What pilot quantity should buyers plan for?
Standard commercial pilot production usually starts from 10,000+ units. A 5,000-unit review may be possible when formula, format, channel plan and launch use case are already clear.
Can we review factory and quality proof first?
Yes. Qualified projects can review relevant factory context, equipment references and quality-document direction during scoping.
Ready for qualification
Turn the current idea into a reviewable pilot brief.
Share the use case, formula status, preferred format, fill volume, target market and launch timing. Proprietary formula details can wait until NDA alignment.