API · FINISHED FORMS · FOOD PRODUCTS

One step to the molecule, a second to the product

Contract development and manufacturing of active pharmaceutical ingredients, finished dosage forms and food products — with a meticulous approach to creating or designing around intellectual property.

PHZAPPA · DEVELOPMENT SYSTEM
3
production verticals
RF·EAPO
patent jurisdictions, extendable worldwide
GMP
quality benchmark
IP
at the initial analysis we propose paths to protect or design around

We work with highly qualified partners across all areas — from synthesis to regulatory filings.

A lab, manufacturing and patent expertise in one team.

PHZAPPA combines chemistry, process technology and legal strategy. We take a product from idea and substance synthesis through to a validated form and a registration dossier — while building the patent perimeter that strengthens the client’s market position.

Development and manufacturing of API, dosage forms and food products

We build a full production cycle for the final product that does not depend on regulatory policy: every production stage is held as the client’s intellectual property.

A · API

API

Synthetic route design, substance production, impurity control and DMF preparation.

B · FDF

Finished dosage forms

Practically every available dosage form, tailored to your site.

C · FOOD

Food products

Functional ingredients and nutraceuticals: recipes, safety, stability, originality.

Every project leaves behind an asset, not just a product

We deliberately create intellectual property — patents related to the substance, composition or technology — so the client gains a defensible market position.

  • IP·1Patent landscapingFreedom-to-operate (patent clearance) analysis and white-space search before development starts.
  • IP·2RF & EAPO filingsDrafting and prosecution of applications in national and Eurasian jurisdictions, plus international filings with follow-up prosecution in any chosen country.
  • IP·3Position defenseOffice-action responses and support in third-party infringement disputes, designing around or challenging patents.

“Without deviation from the norm, progress is not possible.”

F. Zappa

Development and patenting process

A transparent route — from first brief to rights transfer and scale-up.

1

Brief & landscape

Goals, patent search and patent-clearance assessment.

2

Development

Substance synthesis and formulation, analytics and stability.

3

Patenting

Filings on synthesis technologies, composition and other position-strengthening features and technologies in RF and EAPO.

4

Scale & transfer

Production, validation and transfer of rights to the client.

Open to investment on both horizons

The company is ready to attract investment both into expanding its own CDMO capacity and into drug development — generic and original.

INV · 1

CDMO expansion

Investment into in-house manufacturing and laboratory capacity across all verticals.

INV · 2

Drug development

The investor becomes the principal beneficiary, while we take on every stage of development and registration.

INV · 3

Ready portfolios

We have already assembled several investment portfolios that we are ready to offer to investors.

Discuss participation
Confidential

Portfolio disclosed on request

Active projects and candidates are under NDA. Pipeline contents and readiness stages are shared with partners and investors after a confidentiality agreement is signed.

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Get in touch

Tell us about the task — we’ll respond on development, manufacturing and patent options.