Impact-driven

Biosimilars

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Biosimilarity isn’t discovered. It’s engineered.

Precision in every molecule.

Your pure-play
biosimilar developer with an
international track record.

Built to accelerate biosimilar pipelines.

Approved biosimilars

8

Years biologics expertise

12+

Regulatory standards

EMA · FDA

Partners worwide

8

Operating from Zug

Switzerland

Global reach

EU · US · MENA +

WHAT WE DO

We produce impact
driven biosimilars. From
concept to end market.

that most biosimilar programs don’t fail on science. They fail at the transitions.

The molecule isn’t the risk.
The transitions are.

is to keep every program seemlessly moving as one system, from concept to commercial supply.

Full biosimilar lifecycle.
One global development strategy.

We know

Our goal

Swiss engineered, supplied globally

Why partners trust us.

key pillars

A foundation
for reach

We build every program to be regulatory-ready across geographies, giving our commercial partners the fastest possible path to their markets.

A clean track
record

Development pathways built on regulatory rigor, so partners commercialize with certainty. Every product we’ve brought to approval cleared without regulatory pushback.

Built for continuity

Coordinated manufacturing and distribution networks designed to keep supply steady, even at scale.

One point,
full orchestration

A single accountable partner coordinating best-in-class development, manufacturing and commercial supply — so partners can focus on getting products to market.

Work with us

From concept
to commercial supply

We cover full biosimilar lifecycle

how it works

We cover the full biosimilar lifecycle

Momentum doesn't stall at the transitions that matter most.

1

Development

1.1

Designed for scale from day one

1.2

GMP manufacturing built for compliance

1.3

Tech transfer managed end-to-end

1.4

Clinical strategy, study planning, execution & reporting

2

Regulatory

2.1

One unified regulatory strategy

2.2

Dossier build for global submission.

2.3

Inspection readiness from the start

3

Commercial supply

3.1

Supply continuity built into the program

3.2

Launch planning across global markets

3.3

Operational risk managed proactively

4

Lifecycle management

4.1

Post-approval changes handled in-house

4.2

Label extensions and process updates

4.3

Accountable long after launch

Biosimilars don't move themselves. People move them. From molecule to end market.

If you are motivated by complex challenges and meaningful work, we invite you to join us.

Our people are at the heart 
of our success. 


We bring together scientists, engineers, quality experts, and business professionals who share a commitment to excellence and patient impact.

Biosimilars pipeline

Molecules that support long-term economic sustainability.

Program
Reference drug
Therapeutic area
Status
Partner
Ranibizumab
Reference Drug
Lucentis® (Novartis)
Therapeutic area
Ophthalmology
Status
Commercialized
partner
Teva, Zydus
Natalizumab
Reference Drug
Tysabri® (Biogen)
Therapeutic area
Multiple sclerosis
Status
Commercialized
partner
Sandoz
Vedolizumab
Reference Drug
Lucentis® (Novartis)
Therapeutic area
Ophthalmology
Status
Commercialized
partner
Teva, Zydus
Ocrelizumab
Reference Drug
Tysabri® (Biogen)
Therapeutic area
Multiple sclerosis
Status
In development
partner
Sandoz
Guselkumab
Reference Drug
Tysabri® (Biogen)
Therapeutic area
Multiple sclerosis
Status
In development
partner
Sandoz
trusted worldwide

Meet the team of experts
behind every program

Deep expertise. Lean by intention.

Full Name
Role or position
Full Name
Role or position
Full Name
Role or position
Full Name
Role or position
Full Name
Role or position

The right partner changes everything

Our partnerships are built on trust, ownership,
and long-term commitment.

Let’s build together