ABOUT US

An African pharmaceutical company, scientific and institutional

Tsissa Medicines is backed by DAMI, a pan-African platform whose ambition is to help build a sovereign, innovative, sustainable and integrated African pharmaceutical industry.

Mission & vision

Our mission

To develop, manufacture and make accessible pharmaceutical solutions that address the health challenges of the African continent, combining scientific rigour, innovation, local production and the responsible use of resources.

Our vision

An integrated African pharmaceutical industry, able to manufacture, innovate and train on the continent, to international standards.

3
industrial hubs
14
pipeline countries
4
strategic pillars

PLACEHOLDER — figures to be confirmed.

Our history

The stages of an industrial build-up

STAGE 01

Founding

Incorporation of Tsissa Medicines within the DAMI ecosystem and definition of its pharmaceutical positioning.

STAGE 02

Structuring

Development of the quality, industrial and regulatory strategy, and first institutional partnerships.

STAGE 03

Angola Hub

Activation of the first industrial hub in Central and Southern Africa.

STAGE 04

Expansion

Development of the Côte d'Ivoire and Kenya hubs and expansion of the country pipeline.

PLACEHOLDER — milestones and dates to be confirmed.

PORTRAIT — executive management
A word from our CEO
“Building an African pharmaceutical industry is long-term work: it calls for scientific rigour, lasting partnerships and the constant transfer of skills.”
First name Last name
Chief Executive Officer — PLACEHOLDER
Governance

Leadership and governance

PORTRAIT
First name Last name
Executive management

Placeholder biography — industrial and pharmaceutical background.

PORTRAIT
First name Last name
Scientific affairs

Placeholder biography — pharmaceutical research and development.

PORTRAIT
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Industrial operations

Placeholder biography — pharmaceutical manufacturing and engineering.

PORTRAIT
First name Last name
Regulatory affairs

Placeholder biography — quality and regulatory compliance.

PLACEHOLDER — fictional profiles. To be replaced with approved profiles.