Clinical Manufacturing

Clinical Manufacturing

Products
Clinical Manufacturing
Clinical Manufacturing

Information

.Integrated drug development service (CRO/CDMO) including clinical manufacturing and management. The range of activities offered by Bluepharma includes: - Clinical material cGMP manufacturing - Clinical supply management - clinical material - placebo - packaging - labeling - QP release - shipping & returns - Clinical Development and Medical Affairs (CDMA) support - Regulatory support, including the compilation of CMC and IMPD 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,
Distribution Areas
OceaniaNorth America (USA, Canada)Middle East Region (e.g. UAE)Central America (e.g. Mexico)East Asia (e.g. China, Japan, Korea)Europe - EU countriesSouth America (e.g. Brazil, Colombia)
Supplied From
Portugal
All categories
Contract Development and Manufacturing Organisations (CDMOs) and Contract Manufacturing Organisations (CMOs)Clinical Trials Phase I to IVContract Manufacturing of Dosage Form DrugsContract Research Organisations (CROs)Services
Main Categories
Contract Development and Manufacturing Organisations (CDMOs) and Contract Manufacturing Organisations (CMOs)Contract Research Organisations (CROs)
BluepharmaThe Bluepharma Group is today one of the most entrepreneurial and innovative in the pharmaceutical sector, having already achieved remarkable prestige in the most demanding international markets. Bluepharma Group offers a set of capabilities from research, pre-formulation, formulation development, up to commercial manufacturing (including HPAPI), and two sites, including one that is dedicated to High Potent API. Bluepharma also supports non-clinical and clinical stages, including logistics and RA support (IMP, CMC) with a dedicated GMP facility for the handling o...

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