Making commercial generics commercially successful
Let’s make your APIs a global success story.
With our world-class expertise and resources, we’ll give you complete support and customized services around the molecule. Then you can launch with real impact and constantly meet demand.
All you need to do is concentrate on perfecting your APIs: we’ll take care of absolutely everything else. Our complete generic API packages include comprehensive documentation and first-rate manufacturing, getting you to market quickly.
Perfect your generic APIs
Purity is guaranteed – our rigorous quality management system covers the whole process, from raw materials to delivery.
Since we manufacture some of our own starting materials, we can ensure a safe and sustainable supply chain. And you’ll get consistent batch-to-batch quality, helping you build a reputation for excellence.
We’ll help you produce large scales of quality, affordable generic medicines for those who need them most.
Meet demand head-on
Let us simplify your path to API success. By applying the latest technology and manufacturing techniques, we remove barriers to the widespread supply of cost-effective medicines. Together with you, we’ll tackle any challenges along the way, using our expertise and capacity to produce high-quality generics. Plus, you can scale production up as you need, from quantities in grams right up to hundreds of kilos.
A peptide API track record you can trust
We’re proud of our many long-term supply agreements on generic API, including partnerships with AstraZeneca and Debiopharm. You’ll be following in fine footsteps: just take a look at some of the many APIs we’ve helped bring to market.
API | CEP/DMF | Application | Location |
---|---|---|---|
Atosiban | DMF | Reproductive Medicine | CH |
Bivalirudin | DMF | Cardiovascular Disease | CH |
Buserelin | DMF | Oncology, Reproductive Medicine | CH |
Calcitonin | DMF | Paget‘s disease, Hypercalcemia and Osteoporosis | USA |
Glucagon | DMF | Diabetes Mellitus | CH |
Gonadorelin Acetate | CEP / DMF | Oncology, Reproductive Medicine | CH |
Goserelin Acetate | CEP / DMF | Oncology, Reproductive Medicine | CH |
Icatibant Acetate | DMF | Hereditary Angioedema | CH |
Lanreotide | DMF | Oncology | USA |
Leuprolide Acetate | CEP / DMF | Oncology | CH |
Octreotide Acetate | CEP / DMF | Oncology | CH |
Somatostatin | CEP | Gastritis | CH |
Teriparatide Acetate / pTH (1-34) (human) | DMF | Osteoporosis | USA |
Tetracosactide | DMF | Oncology, Diagnostics | CH |
Triptorelin Acetate | DMF | Oncology, Reproductive Medicine | CH |
Triptorelin Pamoate | DMF | Oncology, Reproductive Medicine | CH |
(Arg8)-Vasopressin | DMF | Diabetes Insipidus | USA |
Liraglutide | DMF | Diabetes Mellitus | USA/CH |
Semaglutide* | DMF | Diabetes Mellitus | CH |
Small Molecule API
All small molecule API sold to tenth of tons by Bachem are manufactured at our site in Vionnaz, Switzerland.
Pipeline
Generic API | Application |
---|---|
Glepaglutide* | Short Bowel Syndrome & others |
Setmelanotide* | Obesity |
* Bachem provides this product solely for uses within the scope of any statute or law providing for an immunity, exemption, or exception to patent infringement (“Exempted Uses”), including but not limited to 35 U.S.C. § 271(e)(1) in the United States, the Bolar type exemption in Europe, and any corresponding exception to patent infringement in any other country. lt is the sole responsibility of the purchaser or user of this product, and the purchaser or user of this product agrees to engage only in such Exempted Uses, and to comply with all applicable intellectual property laws and/or regulations. The purchaser of this product agrees to indemnify Bachem against all claims in connection with the performance of the respective commercial agreement (e.g. supply agreement) and possible infringements of intellectual property rights.
Why work with us?
- You come first – Your requirements become our requirements: we’re built on first-rate customer service.
- Excellence – You can rely upon our commitment to quality, backed by half a century of expertise in generics development and production.
- Expertise – Work with our highly skilled, innovation-obsessed team
- Internationally approved – We’re fully GMP compliant, with facilities inspected by the FDA, EMA and Swissmedic.
- Sustainability – We firmly believe long-term business success is driven by ethical behavior and integrity, so we’re dedicated to improving our social, economic and environmental sustainability.
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