We are very happy to attend next 2nd ADC Analytical Development Summit 2023 of Boston, organized by Hanson...
We are happy to participate at American Biomanufacturing Summit 2023 organized by Generis. Designing a new future for...
BSP Pharmaceuticals S.p.A. is proud to announce its presence at the next DCAT Week in New York City. DCAT Week is the...
BSP Pharmaceuticals is proud to announce Its participation to the 13th European edition of World ADC Summit. World ADC...
We are very happy to attend the 3rd Annual Highly Potent APIs Summit 2023 organized online by Qepler from 22nd to 24th...
We are very happy to attend the 2nd Next-Generation Conjugates Summit of Boston 2023, organized by Hanson Wade from...
We are very happy to attend the “Come trasformare una fabbrica farmaceutica in una Smart Factory” event of Rome...
In 2022, CPhI Worldwide becomes CPHI Frankfurt: an event that will take place in-person and online from the 28th...
For its September issue, PHARMAnetwork has asked the CEOs of major CDMOs in Europe and the US to give their reactions...
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
