For US pharma companies, developing lyophilized and liquid formulations is crucial to achieving their drug development aims. Recognizing this, Biopharma Technology LLC’s CDMO lyophilization services and solutions future proof these objectives by enabling organizations to create stable and long-lasting products at scale.
Our services include:
- Material characterization (including FDM/ lyophilization microscopy)
- Proof-of-concept studies
- Formulation development for liquid formulations and lyophilized products
- Process audits, characterization and development
- Lyophilization design space
- Stability studies
- Comparative process studies
- Technical transfer and scale up
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Why Choose Biopharma Technology LLC?
By partnering with Biopharma Technology LLC, our highly-experienced team provides you with expertise and advice at every stage of your research and development (R&D) project – from product and process optimization through to troubleshooting and scale up.
Biopharma Technology LLC’s flexible pharma CDMO services are tailored to the specific requirements of organizations working across the pharmaceutical, biotech and medical devices industries. We can support the development of numerous product types, including:
- Antibiotics
- Hormones
- Peptide
- Oligonucleotides
- Proteins
- Monoclonal antibodies
- ADCs
- Nanoparticles
- Viral vectors
- mRNA vaccines
- Cells and stem cells
- Human and animal tissues
- Plasma derivate product
- Microbiome
- Probiotics
- Aerobic and anaerobic bacteria
- Collagen
Additional Information on Our Pharma CDMO Solutions



When completing material characterisation, Biopharma Technology LLC examines, measures, and determines the chemical, microstructure and physical properties of a material using a range of analytical methods, techniques and tools. Insights gained from this service can inform and enhance your future formulation development plans.
In the initial phases of product development, we complete proof of concept and feasibility studies. Alongside early-stage development and process audits, this helps you to build your future production plans on solid foundations by establishing your sample’s reliability, integrity and viability from the outset.
From lyophilization-cycle development and process reviews to production, packing and shipping, we provide a suite of R&D and analysis solutions for those working in the pharmaceutical sector. When collaborating with us, our team of expert scientists are on-hand throughout every phase of your project to help you to achieve your desired outcomes.
Our scientists support projects of various sizes and scopes – from larger scale formulation projects to smaller trouble-shooting processes. By partnering with us, we can help you to quickly upscale your project in a cost-efficient manner.
Our specialist team offers ad hoc consultancy services which help you to maximize return on investment when developing your formulations, internal processes and future plans. We provide you with practical insights that you can apply immediately to elevate your lyophilization products and methodology.
Using FDM (freeze drying/ lyophilization microscopy) analysis, you can identify critical events throughout your product’s lyophilization cycle, including instances of structural collapse or annealing. This information can be utilized to determine the next steps of your lyophilization cycle and process.


