Category and country

Manufacturing companies in Switzerland

4 manufacturing profiles in Switzerland. Every profile is hand-reviewed with leadership, certifications, and public sources.

Profiles4
Verified4
With certifications4
Cities4
Category view

Where does manufacturing cluster in Switzerland?

Basel (1), Bubendorf (1), Burgdorf (1), and Lachen (1) Most visible profiles: Octapharma, Sandoz, Bachem, and Ypsomed.

Category view

Which standards are already visible?

GMP (3) and ISO-13485 (1) Latest review: 14 March 2026. Review cycle: March 2026.

Full list

Manufacturing profiles in Switzerland

4 profiles match the active filter.

Current review cycle

Octapharma

LachenSwitzerlandManufacturing

Lachen plasma and recombinant therapeutics anchor with a large international manufacturing and product-supply network.

Lead
Wolfgang MarguerreChairman and Chief Executive Officer
Scale
Global biologics manufacturing and supply
0 sources79d reviewGMP plasma-product manufacturingGlobal biologics quality systems
Current review cycle

Sandoz

BaselSwitzerlandManufacturing

Basel-headquartered generics and biosimilars anchor operating a global regulated manufacturing network across essential medicines.

Lead
Richard SaynorChief Executive Officer
Scale
Global regulated medicines supply
0 sources79d reviewGMP medicines manufacturingGlobal generics and biosimilars quality systems
Current review cycle

Bachem

BubendorfSwitzerlandManufacturing

Bubendorf peptide and oligonucleotide manufacturing anchor with a global API and GMP supply role for advanced therapeutics.

Lead
Anne-Kathrin StollerChief Executive Officer
Scale
Global GMP manufacturing
0 sources79d reviewGMP peptide manufacturingGlobal quality systems
Current review cycle

Ypsomed

BurgdorfSwitzerlandManufacturing

Burgdorf injection-device and drug-delivery manufacturing anchor supporting regulated self-injection and digital-care products.

Lead
Simon MichelChief Executive Officer
Scale
Global delivery-device manufacturing
0 sources79d reviewISO 13485 active medical-device quality systemRegulated delivery-device manufacturing
Related brief

Read deeper on this category

Market brief

BIO CITY Vilnius: Northway Biotech’s Biotechnology City Outside Vilnius — Capabilities, Anchor Tenant, and the 2026 Build-Out

What the BIO CITY biotechnology city in Vilnius is, how Northway Biotech operates as the 2026 anchor tenant, which capabilities are live at BIO CITY Vilnius today, and how the multi-phase biotech city build-out is progressing — with sources.

Open brief
FAQ

Frequently asked questions on this category

What is the difference between a manufacturer and a CDMO?
A manufacturer primarily produces its own drug substance, drug product, or device for its own pipeline or commercial supply. A CDMO (Contract Development and Manufacturing Organization) takes external programs from other companies — process transfer, scale-up, contract production. Some companies operate as both: manufacturing their own pipeline AND offering excess capacity to external clients.
Which European countries have the most manufacturing capacity?
Germany leads by industrial depth (Boehringer Ingelheim, Bayer, BioNTech production, Merck KGaA). Switzerland concentrates premium-tier sites (Roche, Novartis manufacturing). Denmark anchors aseptic/biologics scale (Novo Nordisk). Sweden adds AstraZeneca's Gothenburg base. Poland is competitive on cost (Polpharma, Adamed). Lithuania and Estonia have growing biologics manufacturing (Northway, Icosagen).
What certifications should a biotech manufacturer hold?
For drugs and biologics: GMP (essential, country-specific national authority enforces in EU). For medical devices: ISO 13485 + CE marking under MDR/IVDR. For US-bound supply: FDA inspection. For nonclinical studies: GLP. Use the /compliance pages on this directory to filter by specific markers — every published company has its certification context documented and source-backed.
How are manufacturers verified in this directory?
Every profile is hand-reviewed: leadership confirmed by primary source, physical site address sourced from official disclosures, regulatory matrix (GMP / ISO-13485 / GLP / FDA-Inspected) backed by certification documents, and a registry note explaining current operating context and production scope.
Next step

Compare companies or open the wider market.

Use the compare tool to view two or three companies side by side, or open the country hub for the full market view.