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.

GMP
Certified facility
Compliant
Formulas
Reverse
Timeline planning
Stability
Study protocols
Private
Label
Ready
Our Product Development Process

Three phases, from brief to shipment.

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.

FAQ

Common questions on product development.

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.