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Pharma CDMO Services

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Biopharma Group's highly experienced team of scientists provide a wide range of end to end, contract R&D and pharma CDMO services. We aim to work alongside you throughout the entire process – from R&D through to validation, verification and manufacturing.

Biopharma Group is equipped to provide aseptic manufacturing for global customers within the pharmaceutical, diagnostic, medical device and biotech sectors internationally. If you do not have access within your own facility, our comprehensive services aim to assist in product and process optimisation, cycle development, product troubleshooting and scale-up.

We also maintain the capability to provide pharma CDMO formulation development services to help improve the stability of a formulation - ensuring that a product is stable in a liquid and/or freeze-dried format and aiding in excipient selection.

We are proud to have a team of experts able to provide specialist support, educated to PhD level in freeze drying, and/ or related sciences - ensuring our work is of the highest standard and quality, informed by individuals who are consistently active within the industry.

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About us

Biopharma Group CDMO provides extensive services covering R&D, consultancy, and GMP manufacturing (for preclinical and clinical phases) for pharmaceuticals, diagnostics, and biotechnology sectors.

Biopharma Group excels in contract R&D for pharmaceuticals and biological materials, offering expertise in both dried product and liquid formulations. With dedicated in-house facilities and expert scientists, we provide a wide array of services ranging from proof of concept studies to formulation and cycle development, as well as pre- and post-process analysis, and non-GMP production.

In the near future, our GMP suite will cater to the needs of small batch, first-in-human (FIH) clinical trials production. Our expertise in this area is supported by extensive experience in freeze drying spanning over 35 years. This positions Biopharma Group as a global centre for drying process-related projects. Additionally, we have recently focused on enhancing efficiencies in lyobead processing through the development of a lyobead generator, ensuring rapid and accurate results.

Our Services & Solutions:

Biopharma Group offers a diverse array of services and inventive solutions, covering GMP production, liquid and lyophilized formulation development, and beyond, all customized to meet the specific requirements of the biopharmaceutical sector.

Pharma CDMO Services
Biopharma Group is a dynamic and adaptable CDMO partner within the pharmaceutical sector, providing extensive R&D and manufacturing services. Our dedication to Quality by Design (QbD) and Design of Experiment (DoE) approaches fuels innovative and streamlined drug formulation and lyophilization process enhancements.

GMP Production
Biopharma Group's GMP freeze-drying production facility, compliant with Annex 1 standards, aids partners in transitioning their products from the R&D phase to clinical manufacturing. Situated in the UK, the facility is tailored to facilitate small-batch manufacturing of both cytotoxic and non-cytotoxic products for first-in-human (FIH) trials, providing rapid, efficient GMP manufacturing alongside flexible solutions.

Diagnostic CDMO Services
Dealing with challenges such as limited shelf life, cold chain supply, or product performance? Biopharma Group's diagnostic services provide troubleshooting solutions, including audits, optimization, and reformulation. Our comprehensive custom packing facility handles everything from individual kits to final shipper cartons. With our expertise in secure worldwide shipping across temperatures ranging from -80°C to ambient, you can rely on us to handle your samples with care at every stage.
Cytotoxic & High Potency Samples Handling/ Processing
Biopharma Group boasts significant expertise in managing cytotoxic and highly potent active pharmaceutical ingredient (HPAPI) samples, prioritizing the safety of all stakeholders and safeguarding product integrity. With a robust emphasis on containment and protective protocols, we offer the necessary expertise to handle cytotoxic compounds with stringent safety measures.

Analytical Lyo Instruments
Biopharma Group is proud to introduce its cutting-edge analytical lyophilization instruments, featuring the Lyostat freeze-drying microscope (FDM), Lyotherm DTA and impedance analyzer, MicroPress, and the latest addition, the LyobeadPRO lyobead generator. These advanced tools are crafted to assist professionals in freeze-drying technologies for both production and research endeavors. As part of our dedication to excellence, we consistently refine and upgrade these instruments to offer state-of-the-art solutions that align with the dynamic needs of the industry.

Lyo Training Courses
Biopharma Group provides thorough lyophilization training programs tailored to acquaint you with the fundamentals of lyophilization processes. These courses encompass diverse subjects, including theory, practical applications, best practices, and troubleshooting methods. Whether you're new to lyophilization or aiming to refine your expertise, our training programs offer valuable insights and hands-on learning opportunities. You can participate in sessions held at our Winchester, UK site, or opt for training at your location, via online webinars, or through pre-recorded eLearning modules.

At Biopharma Group, we recognize the crucial importance of engaging with a specialist at the outset of the lyophilization formulation development process, particularly when collaborating with a CDMO. Whether you seek a comprehensive solution spanning from R&D to GMP or non-GMP production, or require assistance with specific aspects of the process, our team consists of committed lyophilization experts. They offer tailored insights into our core services and impartial assessments to help identify the most suitable solutions for your needs.

Our in-house laboratory scientists possess valuable expertise in science and can provide professional insights into our wide range of CDMO services for dried product and liquid formulations. This ensures that you can trust your product or project is in capable hands.