Description
Serán BioScience is a science-driven Contract Development and Manufacturing Organization (CDMO), recognised as a world leader in drug development. Specialising in the transformation of complex compounds into enabling medicines, Serán leverages its extensive knowledge base in physical and chemical science to design robust formulations and engineered solutions tailored to address some of the toughest challenges in the pharmaceutical industry. With a team that boasts decades of experience, Serán adeptly navigates the intricacies of developing complex drug molecules into market-ready products.
Services include:
– Analytical Services
– Blending
– Contract Development and Manufacturing (CDMO)
– Contract Manufacturing (CMO)
– Contract Research (CRO)
– Dosage Form Development
– Drug Delivery Devices
– Drug Design
– Drug Development
– Encapsulation
– Feasibility Studies
– Filling
– Capsule
– Fluid Bed Processing
– Forced Degradation Studies
– Process Development
– Formulation Development
– Controlled Release
– Hot Melt Extrusion
– Manufacturing
– High Containment Operations
– Inhalables
– Oral Drug Delivery
– Peptides
– Powders
– Non-Sterile
– Proteins
– Solid Dosage
– Solutions & Suspensions
– Sustained Release
– Tablets
– Micronization
– Packaging
– Particle Characterization
– Particle Size Analysis
– Particle Size Classification
– Pharmacokinetics
– Pilot-Scale Filling
– Preclinical Testing
– Preclinical Testing Formulations
– Preformulation
– Process Analytical Technology (PAT)
– Process Characterization
– Process R&D
– Process Validation Studies
– Quality QA/QC
– Scale-Up
– Size Reduction
– Spray Drying
– Stability Studies
– Storage
– Sustained Release Delivery Systems
– Technology Transfer
– Laboratory and Analytical Services
– Clinical Dose
– Clinical Packaging
Serán BioScience is committed to delivering exceptional drug development solutions to its clients, ensuring quality and efficacy throughout the process. For more information, please visit seranbio.com.
Capabilities
- Analytical Services
- Blending
- Capsule
- Clinical Dose
- Clinical Packaging
- Contract Development and Manufacturing (CDMO)
- Contract Research (CRO)
- Controlled Release
- Dosage Form Development
- Drug Delivery Devices
- Drug Development
- Encapsulation
- Feasibility Studies
- Filling
- Fluid Bed Processing
- Forced Degradation Studies
- Formulation Development
- High Containment Operations
- Hot Melt Extrusion
- Inhalables
- Laboratory and Analytical Services
- Micronization
- Non Sterile Dosage
- Oral Drug Delivery
- Packaging
- Particle Size Analysis
- Peptides
- Pharmacokinetics
- Pilot-Scale Filling
- Powders
- Preclinical Testing
- Preformulation
- Process Analytical Technology (PAT)
- Process Characterization
- Process Development
- Process Validation Studies
- Proteins
- Quality QA/QC
- Scale-Up
- Size Reduction
- Solid Dosage
- Solutions & Suspensions
- Spray Drying
- Stability Studies
- Storage
- Sustained Release
- Sustained Release Delivery Systems
- Tablets
- Technology Transfer
Contact Information
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