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...
We are very happy to attend next 13th Annual World Multispecific Summit of Boston 2022, organized by Hanson...
_Provider_2022_Logo438x214.jpg)
BSP Pharmaceuticals S.p.A. is pleased to announce that last 8th of September, It won the '9th Annual World ADC Awards...
We are very happy to attend next 13th Annual World ADC Summit of San Diego 2022, organized by Hanson Wade from 6th...
We are proud to be present at World Health Summit Regional Meeting Rome 2022 hosted by Sapienza University of Rome ...
BSP Pharmaceuticals S.p.A. is glad to announce its participation to the next BIO International Convention of San Diego...
We are very happy to attend next ADC Analytical Development Summit 2022 of Boston, organized by Hanson Wade. The...
BSP Pharmaceuticals S.p.A. is proud to participate at the next 7th Annual High Potent Medicines Conference of London...
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
