From formula feasibility to manufacturing transfer.
A scientist-led workflow for oral dissolving film formulation, coating, cutting, packaging and batch documentation. Project specifications guide every production decision.
Illustrative product and workflow photography. Final film appearance and packaging are confirmed during project development.
Four connected manufacturing disciplines.
Formulation R&D
Review ingredients, taste masking, film-former compatibility and achievable unit loading.
Film processing
Evaluate mixing, casting or coating, drying, slitting and cutting against the agreed specification.
Quality control
Define test methods, finished-film controls and batch-wise documentation.
Scale-up & delivery
Review manufacturing transfer, pack protection, order planning and export coordination.
Research experience, applied to film development.
The company profile describes a research center covering more than 4,000 square meters, peptide synthesis and HPLC analytical and preparative resources. Oral film projects use an agreed development and testing scope rather than inheriting peptide specifications automatically.
Our manufacturing base in Shaoxing, Mainland China was established in 2014. HYTANBIO’s Hong Kong entity was founded in 2026 for international business development.
Capacity allocation, sample timing, minimum order quantities and commercial lead times are quoted after reviewing the formula, pack format and production plan.
Documentation matched to the finished project.
A quality dossier begins with the actual formula and manufacturing site. Typical agreed documentation may include ingredient specifications, finished-batch analytical results, identity and content testing, microbial specifications, packaging specifications and stability data. Available documents are confirmed during project review.
Identity & uniformity
Confirm the active identity, blend distribution and finished-film content against the agreed method.
Process & batch records
Define critical process controls and retain batch-wise manufacturing and quality documentation.
Stability & packaging
Evaluate film condition and relevant ingredient attributes in the actual barrier pack over time.
Reference schemes shown in the supplied materials include cGMP, HACCP, Halal, ISO 22000, ISO 9001, Kosher, food-facility registration and Vegan. Availability and applicability are confirmed with current source documents.
Additional supplied qualification reference
This additional supplied image is displayed as source reference material. Current certificate entity, scheme, scope and validity are confirmed with the original documents for the project.
What our manufacturing review needs.
| Input | What we review | What is confirmed |
|---|---|---|
| Formula & actives | Identity, serving expectations, compatibility and sensory constraints | Feasibility, prototype scope and specification |
| Unit film | Dimensions, thickness, flexibility, dissolution and uniformity | Project-specific acceptance criteria |
| Packaging | Barrier, sealing, labels, artwork and carton configuration | Approved packaging brief and artwork |
| Production & export | Volume, availability, destination and documentation needs | Quoted MOQ, schedule and agreed supply terms |
