BSP Pharmaceuticals S.p.A. is glad to announce its participation to the next BIO International Convention of Boston...
BSP Pharmaceuticals S.p.A. is proud to announce Its participation to the 4th Annual World ADC Asia Summit of Incheon...
We are very happy to attend next CPHI North America 2025 of Philadelphia from 20 to 22 May. The CPHI is the event that...
BSP Pharmaceuticals is proud to announce Its participation to the CDMO Live 2025 at World Trade Center of Rotterdam,...
We are very happy to attend next 4th ADC Analytical Development Summit 2025 of Boston, organized by Hanson Wade. We are...
BSP Pharmaceuticals is proud to announce Its participation to the Festival Of Biologics USA 2025 organized by...
We are very happy to attend the 4th Annual Novel Conjugates Summit of Boston 2025, organized by Hanson Wade from 25th...
BSP Pharmaceuticals S.p.A. is proud to announce its presence at the next DCAT Week 2025 in New York City. DCAT Week is...
BSP Pharmaceuticals is proud to announce Its participation to the 15th Annual World ADC Summit of London 2025 organized...
BSP Pharmaceuticals S.p.a. is a Contract Development and Manufacturing Organization (CDMO).
The BSP campus hosts 2 segregated facilities to serve the clients with development from pre-clinical GLP to cGMP manufacturing for clinical and commercial supply of Cytotoxic and High Potent Oncology drugs (OEL < 0,01 µG/M 3 ) and Non-Cytotoxic (up to OEB 6), innovative compounds for Immunotherapy and other therapeutics applications.
Facilities designed to handle small and large molecules as ADCs (conjugation and fill finish), Peptides, Proteins, Oligonucleotides and Nano Medicines.
BSP is technologically developed to meet the needs of innovators, with its High Containment Facility designed to offer a full range of integrated services aimed to support the entire life cycle of a product, from the formulation and process development/optimization, through scale up/scale down studies.
QC laboratories are equipped to run all analytical testing (chemical
and microbiological) on raw materials, components, in process
controls, release and stability testing.
Internal Regulatory Affairs team to manage data collection and document preparation for DMF and CMC
to support filing activities.
HIGH CONTAINMENT and EXPLOSION PROOF manufacturing
facilities with 100% one pass through air handling systems
Supply of > 80 countries (EU, US, JP)
Development labs to support the product lifecycle
Experience on Break through, Emergency Use,
Fast track designated products
Lipid based formulation - State of the art technology to support
lipid based formulations and high sensitive products
(temperature, light, oxygen)
Full range of services from development
to commercial supply
Integrated services for ADCs , manufacturing of conjugation
and fill finish at the same site
Global regulatory support
Import/Export management
Life cycle management with process and product
improvement
Focus on sustainability
