Pharmaceutical development (CDMO) & Exclusive portfolio

From research, pre-formulation, and formulation development, up to commercial manufacturing  (including HPAPI).
Bluepharma offers an integrated drug development service (CDMO) from research, pre-formulation, and formulation development, up to commercial manufacturing  (including HPAPI). Bluepharma also supports non-clinical and clinical stages, including logistics and RA support (IMP, CMC) with a dedicated GMP facility for the handling of high potent APIs covering clinical, registration, and commercial batches  

Our range of technologies covers solid dosage forms (IR and ER), polymer-based solutions, solid dispersions (hot-melt extrusion), oral sprays, oral thin films and complex injectables (LNP) to achieve the best PK profile and customize our solutions for complex products.

The range of activities offered by Bluepharma includes:
•        Pre-formulation studies
•        Formulation development (from lab to commercial scale)
•        Analytical development & validation
•        Stability Studies
•        Clinical supply management
•        Clinical Development and Medical Affairs (CDMA) support
•        Regulatory support, including the compilation of CMC and IMPD
•        Commercial Manufacturing and Supply Chain management
•        Packaging (primary & secondary)
•        Distribution & Logistics

Covering all the life-cycle chain we can reduce the risk and time to market.

We can offer a one-stop-shop service, tailored to our client's needs and expectations.
Schedule a meeting with Bluepharma to know more about our services.