STRATEGY
MEETS
PRODUCT INNOVATION

Scalable processes, validated methods, and controlled environments – seamlessly bridging the gap from R&D to full-scale manufacturing.

Our core competencies in developing plasma derived proteins across all disciplines and development steps until custom manufacturing are built on a foundation of extensive industry expertise, specialized infrastructure, and time-tested methodologies. Within our state-of-the-art R&D facilities, we develop, evaluate, and optimize processes under strictly controlled conditions, ensuring maximum robustness, reproducibility, and regulatory compliance for every project.

Mannheim

Diverse know-how plus solid resource inventory allows PreviPharma the ability to deliver results
at speed, skill and highest quality.

  • Bioprocessing Unit
  • Analytical Unit
  • Laboratory Service
  • Assay Expertise
  • Strategic Research Support: Expert guidance for target validation, Mode of Action (MoA) analysis, and candidate selection
  • Seamless Integration: Close synergy with in-vivo programs to ensure efficient study progression
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Hyerabad

Flexible Manufacturing Services – From lab-scale development to GMP production

  • Preclinical research at pre-qualified, reliable FDA/EMA approved sites
  • From feasibility to IND using established models in multiple indicational areas supported by highly experienced surgeons and teams
  • GMP Manufacturing
  • Clinical trial access
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Process Expertise Across
the entire Value Chain

Seamless Excellence: Mastering Every Step from Source to Solution.
Our comprehensive service spectrum encompasses every critical process step – from the strategic preparation of raw materials to the final formulation of your product.

Preparation & Handling

– Expert management of complex raw materials to ensure optimal starting conditions.
– Paste Suspension Processing: Comprehensive processing of all relevant plasma fractions.
– Fraction Handling: Specialized handling of IgG intermediate fractions, side fractions, and supernatants.

Virus inactivation and removal

– SD-Treatment: Experience with all existing and novel reagents, as well as removing them.
– Low-pH Treatment: A critical step for robust viral reduction.
– Heat Treatment: Specialized thermal processing to ensure product safety.
– Nanofiltration (NF): State-of-the-art filtration for the highest level of viral clearance.

Chromatography

Process Development & Optimization
– Batch chromatography (1 mL to 10 L column volume).
– Continuous chromatography (PCC, SMB, etc.).
– Conversion from batch to continuous processes.
– Downscale modeling of individual process steps.
– DoE and robustness studies.

Media & Resin Development
– Broad resin library including prototypes.
– Resin screening & target optimization.
– Development & testing of new resin prototypes.
– Data packages for plasma-based applications.

Filtration

Depth Filtration
– Filtration areas from 0.0073 m² to 0.1 m² (infusion filters).
– Filter presses (frame width 10–30 cm).
– Filter media library from all manufacturers, including prototypes.
– Process optimization & integration of single-use systems.
– Additional material science analyses.

UF/DF & Formulation

– Ultrafiltration / diafiltration (UF/DF).
– Development of stable, application-specific formulations.
– Alignment with target product profiles and downstream requirements TFF.