Egyptian Pharmaceutical Platform

A registered pharmaceutical portfolio, built over a decade.

A unified Egyptian pharmaceutical group operating two licensed entities, holding a registered portfolio across multiple therapeutic sub-segments of the primary-care market.

Jurisdiction
Arab Republic of Egypt
Regulatory Authorities
EDA · NFSA
Operating Model
Asset-light · Registration-led
01

Adams & Techno Pharma Group is a consolidated Egyptian pharmaceutical platform operating through two sister limited-partnership entities — Adams Pharma and Techno Pharma — both domiciled in Suez and sharing common shareholding and management.

The two entities were founded sequentially to build parallel product pipelines across complementary therapeutic areas under a single operating philosophy: disciplined regulatory practice, selective molecule and dosage-form positioning, and contracted GMP manufacturing through specialist partners.

The Group’s operating model is asset-light. Intellectual property, pharmaceutical registrations, and regulatory licenses are held centrally, while manufacturing and physical distribution are delivered through contracted specialist partners.
02

Two licensed entities, one group platform.

Founding Entity
Adam’s Pharma
Limited Partnership · Established 2014

Adams Pharma is the founding entity of the group, holding the senior EDA toll-manufacturer license and the group’s first fully-registered pharmaceutical product. Operates across primary-care pharmaceutical and food-supplement categories.

Toll LicenseToll / 839
JurisdictionSuez
Registered ProductsPharma & NFSA
Operating Since2014
Sister Entity
Techno Pharma
Limited Partnership · Established 2015

Techno Pharma operates the group’s broader active-registration pipeline, holding the most recently renewed EDA toll-manufacturer license and multiple registered products across cardiovascular, antihypertensive, and women’s-health categories.

Toll LicenseToll / 1055
JurisdictionSuez
License Renewed2025 · Valid to 2035
Operating Since2015
At a Glance

A decade of regulatory discipline.

Operating History
10YRS
Combined years of registered pharmaceutical operation across both entities, established 2014–2015.
Toll Licenses
2
Valid EDA toll-manufacturer licenses, held independently by each sister entity.
GMP Partners
4
Contracted GMP-certified toll-manufacturing partnerships across Egyptian pharmaceutical production.
Therapeutic Focus
15SEG
Therapeutic sub-segments addressed across cardiovascular, GI, women’s health, analgesic, and OTC categories.
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A selection of the Group’s commercially active products. The full registered portfolio is disclosed under confidentiality to qualified parties.

01
Adamshydro®Hydrotalcite 1000mg · Oral SuspensionRegistered under Adams Pharma
Antacid indicated for the symptomatic relief of hyperacidity. Sachet-format oral suspension. Fully registered with the Egyptian Drug Authority under a ten-year license.
Fully Registered
02
Technoprotect®Boswellia + Turmeric · Hard Gelatin CapsuleRegistered under Techno Pharma
Food supplement supporting joint health and movement. Standardized boswellic acid and curcuminoid extracts. NFSA registered, valid through 2029.
Commercially Active
03
Inflabos®Boswellia Serrata · Hard Gelatin CapsuleRegistered under Adams Pharma
Food supplement supporting joint health and natural inflammation response. Single-ingredient standardized extract. NFSA registered, valid through 2029.
Commercially Active
Regulatory Position

Disciplined positioning within the EDA framework.

Pharmaceutical registration in Egypt operates under Chairman Decree 450/2023, a quota-governed framework in which each active ingredient and dosage form admits a limited number of registered alternatives before the relevant category closes to new entrants.

The Group’s portfolio has been constructed with deliberate attention to this framework, with dosage-form selection calibrated to occupy categories offering favorable entry dynamics — a strategic posture maintained consistently across both entities over eight years of building.

“The EDA pricing committee approvals held by the Group represent the slowest and most uncertain step in Egyptian pharmaceutical registration — already completed.”

Primary Regulator
Egyptian Drug Authority
WHO maturity level 3 regulatory authority (certified November 2024).
Food Supplement Regulator
NFSA
National Food Safety Authority — Egyptian supplement registration body.
Governing Framework
Chairman Decree 450/2023
The current EDA pharmaceutical registration and quota framework.
License Status
Both Valid & Current
EDA toll-manufacturer licenses maintained continuously on both entities.
— Strategic Activity

The Group is selectively engaging with qualified parties on long-term strategic matters.

Inquiries of a strategic nature from regulated pharmaceutical institutions, healthcare platforms, and established investment parties are considered on a confidential basis and subject to non-disclosure.

Confidential Inquiry
— Inquiry

Qualified inquiries only.

For inquiries of a strategic nature — including partnership, licensing, or long-term structural discussions — please complete the form. Messages are reviewed within five business days.

Commercial inquiries, regulatory correspondence, and supplier proposals are not handled through this channel.

All substantive discussion proceeds under a mutual non-disclosure agreement executed between the Shareholders of the Group and the inquiring party. No confidential information is released prior to NDA execution.