Custom Healthcare Product Development | Formulation to Manufacturing — Medicka Lab
Custom Product Development
Every custom product starts as a brief.
From feasibility through manufacturing, we build a healthcare product that's genuinely yours — compliant, costed, and market-ready before a single unit ships.
Every custom product moves through the same disciplined path — feasibility, development, and manufacturing — so nothing reaches your shelf untested or unpriced.
DEV-01 / FEASIBILITY
Feasibility
After receiving your brief, we turn it into a concrete plan — the materials, the formula, and the numbers behind it.
Key steps
Identify the right raw materials & packaging
Propose a formula compliant with current regulations
Provide a price quote
Create a reverse timeline
Present a development cost proposal
DEV-02 / DEVELOPMENT
Development
Once you approve the theoretical formula and price, we move from theory to lab-tested, scale-ready product.
Key steps
Laboratory tests & prototypes
Industrial scale-up validation & trials if necessary
Stability study protocols
Test reports & product dossiers
Finalized formula & pricing
DEV-03 / MANUFACTURING
Manufacturing
Your order triggers production — planned, quality-checked, and delivered end to end.
Key steps
Validate final "Bon à Tirer" proofs
Plan supplies
Initiate first-order manufacturing
Quality control on finished products
Ship, deliver & invoice
Why Medicka Lab
A development partner that plans backward from your launch.
Every phase produces a document, a price, or a proof — nothing moves forward on guesswork.
GMP-certified manufacturing
Every batch produced under audited quality standards.
Regulatory-compliant formulas
Every formula built to current regulations from day one.
Transparent cost proposals
Full pricing presented before development begins.
Reverse-timeline planning
A schedule built backward from your target launch date.
Stability study protocols
Shelf-life validated before industrial scale-up.
Full documentation
Test reports and product dossiers for every formula.
Industrial scale-up validation
Lab results confirmed at production scale before launch.
International regulatory expertise
Compliance guidance as your product enters new markets.
From Brief to Delivery
The whole journey, at a glance.
Every step inside feasibility, development, and manufacturing rolls up into four checkpoints.
01
Brief & feasibility
Raw materials, formula, quote, and reverse timeline defined upfront.
02
Lab development
Prototypes, stability protocols, and industrial-scale validation.
03
Manufacturing
First-order production with quality control on finished goods.
04
Delivery & billing
Shipping, delivery confirmation, and invoicing.
Ready to develop your product?
Let's turn your brief into a formula.
Tell us your concept, your market, and your timeline — we'll come back with a formula, a quote, and a reverse timeline to get there.
If your question isn't covered here, request a consultation and we'll answer it directly.
We identify the right raw materials and packaging for your brief, propose a formula that complies with current regulations, provide a price quote, build a reverse timeline, and present a cost proposal for development.
Once you approve the theoretical formula and price, we run laboratory tests and prototypes, validate industrial scale-up with trials if necessary, offer stability study protocols, prepare test reports and product dossiers, and finalize the formula and pricing.
A reverse timeline is a schedule built backward from your target launch date, so every feasibility and development milestone is sequenced to have your product ready for manufacturing on time.
We validate the final Bon à Tirer (Ready for Printing) proofs, plan supplies, run the first order, and conduct quality control on the finished products before shipping.
Yes. Stability study protocols are offered during the development phase to validate shelf life before industrial scale-up.
Yes. A price quote and a full cost proposal are provided during the feasibility phase, before any laboratory work begins.