Nanomedicines

Advancing nanomedicine development for targeted drug delivery and next-generation therapies.

Get to market faster with CPI

At CPI, we support the development, optimisation, and scale-up of nanomedicines, helping you harness nano-formulations for enhanced drug delivery, improved stability, and therapeutic efficacy. 

Our expertise in nanoparticle synthesis, formulation development, and analytical characterisation ensures your innovations meet the highest standards of safety, quality, and performance. Whether working with lipid nanoparticles (LNPs), polymeric carriers, or other targeted drug delivery systems, we provide the tools and infrastructure to accelerate your journey from preclinical research to clinical application. 

Droplets of a liquid.

Nanomedicines

Advancing nanomedicine development for targeted drug delivery and next-generation therapies.

Get to market faster with CPI

At CPI, we support the development, optimisation, and scale-up of nanomedicines, helping you harness nano-formulations for enhanced drug delivery, improved stability, and therapeutic efficacy. 

Our expertise in nanoparticle synthesis, formulation development, and analytical characterisation ensures your innovations meet the highest standards of safety, quality, and performance. Whether working with lipid nanoparticles (LNPs), polymeric carriers, or other targeted drug delivery systems, we provide the tools and infrastructure to accelerate your journey from preclinical research to clinical application. 

Droplets of a liquid.

Nanomedicines

Advancing nanomedicine development for targeted drug delivery and next-generation therapies.

Get to market faster with CPI

At CPI, we support the development, optimisation, and scale-up of nanomedicines, helping you harness nano-formulations for enhanced drug delivery, improved stability, and therapeutic efficacy. 

Our expertise in nanoparticle synthesis, formulation development, and analytical characterisation ensures your innovations meet the highest standards of safety, quality, and performance. Whether working with lipid nanoparticles (LNPs), polymeric carriers, or other targeted drug delivery systems, we provide the tools and infrastructure to accelerate your journey from preclinical research to clinical application. 

  • SGS Quay Pharma
  • BoobyBiome
  • RNAssist
  • Intract Pharma
  • Pharmidex
  • AstraZeneca

What we offer

Whether you need technical expertise, lab-based development, or process optimisation, our tailored approach ensures you have the right support at every stage.

What we offer

Whether you need technical expertise, lab-based development, or process optimisation, our tailored approach ensures you have the right support at every stage.

What we offer

Whether you need technical expertise, lab-based development, or process optimisation, our tailored approach ensures you have the right support at every stage.

Nanomedicine process development and optimisation

Accelerate your nanomedicine innovation with our comprehensive formulation and process development support: 

  • Formulation development for active payloads, delivery systems, and excipient selection. 

  • Screening for enhanced stability, targeted delivery, and sustained release. 

  • Batch and continuous manufacturing of nanoparticle formulations. 

  • Solvent removal, buffer exchange, isolation, lyophilisation, and concentration. 

  • High-throughput formulation screening and characterisation. 

  • Tech transfer support for seamless scale-up. 

  • Digital modelling to optimise process parameters and predict product quality. 

These capabilities ensure robust, scalable, and high-performance nanomedicine development. 

Nanomedicine process development and optimisation

Accelerate your nanomedicine innovation with our comprehensive formulation and process development support: 

  • Formulation development for active payloads, delivery systems, and excipient selection. 

  • Screening for enhanced stability, targeted delivery, and sustained release. 

  • Batch and continuous manufacturing of nanoparticle formulations. 

  • Solvent removal, buffer exchange, isolation, lyophilisation, and concentration. 

  • High-throughput formulation screening and characterisation. 

  • Tech transfer support for seamless scale-up. 

  • Digital modelling to optimise process parameters and predict product quality. 

These capabilities ensure robust, scalable, and high-performance nanomedicine development. 

Analytical method development and stability testing

Ensure the quality, integrity, and stability of your nanomedicines with our analytical expertise: 

  • Particle size, surface charge, and morphology analysis (DLS, SEM, AFM). 

  • Chemical composition assessment (HPLC, GC, FT-IR, Raman spectroscopy). 

  • Drug loading, release kinetics, and bioavailability studies. 

  • Pharmacopoeial testing for regulatory alignment. 

  • Real-time and accelerated stability studies (-80°C to 100°C). 

  • Data-driven insights to inform formulation refinement and shelf-life prediction. 

These capabilities de-risk development and support product quality throughout the lifecycle. 

Analytical method development and stability testing

Ensure the quality, integrity, and stability of your nanomedicines with our analytical expertise: 

  • Particle size, surface charge, and morphology analysis (DLS, SEM, AFM). 

  • Chemical composition assessment (HPLC, GC, FT-IR, Raman spectroscopy). 

  • Drug loading, release kinetics, and bioavailability studies. 

  • Pharmacopoeial testing for regulatory alignment. 

  • Real-time and accelerated stability studies (-80°C to 100°C). 

  • Data-driven insights to inform formulation refinement and shelf-life prediction. 

These capabilities de-risk development and support product quality throughout the lifecycle. 

Preclinical material supply for in vitro and in vivo testing

Support preclinical and clinical progression with expert material production: 

  • Low-bioburden and endotoxin-free nanomedicine formulations. 

  • Scalable supply for in vitro and in vivo studies. 

  • Process robustness for clinical readiness. 

  • Documentation and tech transfer support for GMP compliance. 

  • In vitro and in vivo screening via the Intracellular Drug Delivery Centre. 

  • GMP manufacturing capability via our RNA Centre of Excellence for clinical trial supply. 

These capabilities ensure a smooth transition from discovery to clinical trials. 

Preclinical material supply for in vitro and in vivo testing

Support preclinical and clinical progression with expert material production: 

  • Low-bioburden and endotoxin-free nanomedicine formulations. 

  • Scalable supply for in vitro and in vivo studies. 

  • Process robustness for clinical readiness. 

  • Documentation and tech transfer support for GMP compliance. 

  • In vitro and in vivo screening via the Intracellular Drug Delivery Centre. 

  • GMP manufacturing capability via our RNA Centre of Excellence for clinical trial supply. 

These capabilities ensure a smooth transition from discovery to clinical trials. 

How we support you

From discovery to commercialisation, we enable scalable, cost-effective, regulatory-compliant, and environmentally conscious pharmaceutical innovations.

How we support you

From discovery to commercialisation, we enable scalable, cost-effective, regulatory-compliant, and environmentally conscious pharmaceutical innovations.

How we support you

From discovery to commercialisation, we enable scalable, cost-effective, regulatory-compliant, and environmentally conscious pharmaceutical innovations.

Demonstrate the benefits of your nanomedicine innovation

Accelerate early-stage development and build investor confidence with: 

  • Rapid, cost-effective proof-of-concept studies. 

  • Testing of nano-formulations in industry-relevant conditions. 

  • Optimisation of nano-based drug delivery systems for performance and stability. 

Demonstrate the benefits of your nanomedicine innovation

Accelerate early-stage development and build investor confidence with: 

  • Rapid, cost-effective proof-of-concept studies. 

  • Testing of nano-formulations in industry-relevant conditions. 

  • Optimisation of nano-based drug delivery systems for performance and stability. 

Prove manufacturability and scalability

De-risk scale-up through: 

  • Manufacturability assessments of nanoparticle formulations. 

  • Optimisation for yield, reproducibility, stability, and cost efficiency. 

  • Integration of continuous processes and automation for clinical and commercial readiness. 

Prove manufacturability and scalability

De-risk scale-up through: 

  • Manufacturability assessments of nanoparticle formulations. 

  • Optimisation for yield, reproducibility, stability, and cost efficiency. 

  • Integration of continuous processes and automation for clinical and commercial readiness. 

Assess and demonstrate commercial viability

Gain the insight and evidence you need to unlock investment and market entry: 

  • Commercial feasibility studies for nanomedicines. 

  • Validation of scalable manufacturing processes. 

  • Support transitioning from preclinical development to launch. 

Assess and demonstrate commercial viability

Gain the insight and evidence you need to unlock investment and market entry: 

  • Commercial feasibility studies for nanomedicines. 

  • Validation of scalable manufacturing processes. 

  • Support transitioning from preclinical development to launch. 

Streamline regulatory compliance

Reduce time to market and meet global quality expectations: 

  • Development of robust analytical methods for regulatory submission. 

  • Quality assurance and GMP documentation aligned to compliance standards. 

Streamline regulatory compliance

Reduce time to market and meet global quality expectations: 

  • Development of robust analytical methods for regulatory submission. 

  • Quality assurance and GMP documentation aligned to compliance standards. 

Secure strategic partnerships

Connect with the right people to move forward faster: 

  • Access to nanomedicine specialists, manufacturers, and academic collaborators. 

  • Stronger, more resilient supply chains for nano-formulations. 

  • Partnerships to tackle industry-wide nanomedicine challenges. 

Secure strategic partnerships

Connect with the right people to move forward faster: 

  • Access to nanomedicine specialists, manufacturers, and academic collaborators. 

  • Stronger, more resilient supply chains for nano-formulations. 

  • Partnerships to tackle industry-wide nanomedicine challenges. 

  • Stainless steel process equipment skid installed in a pharmaceutical cleanroom.
    White oval tablets in the tray of a pharmaceutical counting and inspection machine.
  • Gowned scientist using a pipette to transfer a sample into a tube inside a laminar flow hood.
    CPI scientist in a lab coat and safety glasses using a pipette at a laboratory bench.
  • CPI scientist in a blue lab coat operating an ambr 250 automated bioreactor system with a tablet.
  • Row of capped glass vials moving along a pharmaceutical filling line.
    CPI scientist in safety glasses using a pipette to handle a pink sample in a laboratory.
  • CPI scientist drawing a process diagram on a glass screen in a laboratory.
    CPI scientists in blue lab coats operating analytical equipment in a laboratory.
  • Gloved hand placing a strip of PCR tubes containing blue liquid into a thermal cycler.
  • Stainless steel process equipment skid installed in a pharmaceutical cleanroom.
    White oval tablets in the tray of a pharmaceutical counting and inspection machine.
  • Gowned scientist using a pipette to transfer a sample into a tube inside a laminar flow hood.
    CPI scientist in a lab coat and safety glasses using a pipette at a laboratory bench.
  • CPI scientist in a blue lab coat operating an ambr 250 automated bioreactor system with a tablet.
  • Row of capped glass vials moving along a pharmaceutical filling line.
    CPI scientist in safety glasses using a pipette to handle a pink sample in a laboratory.
  • CPI scientist drawing a process diagram on a glass screen in a laboratory.
    CPI scientists in blue lab coats operating analytical equipment in a laboratory.
  • Gloved hand placing a strip of PCR tubes containing blue liquid into a thermal cycler.
  • Stainless steel process equipment skid installed in a pharmaceutical cleanroom.
    White oval tablets in the tray of a pharmaceutical counting and inspection machine.
  • Gowned scientist using a pipette to transfer a sample into a tube inside a laminar flow hood.
    CPI scientist in a lab coat and safety glasses using a pipette at a laboratory bench.
  • CPI scientist in a blue lab coat operating an ambr 250 automated bioreactor system with a tablet.
  • Row of capped glass vials moving along a pharmaceutical filling line.
    CPI scientist in safety glasses using a pipette to handle a pink sample in a laboratory.
  • CPI scientist drawing a process diagram on a glass screen in a laboratory.
    CPI scientists in blue lab coats operating analytical equipment in a laboratory.
  • Gloved hand placing a strip of PCR tubes containing blue liquid into a thermal cycler.
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Trusted by leading organisations

Showing slide 1 of 1
BoobyBiome

CPI was an excellent partner, aiding in demonstrating the manufacturing feasibility of our top bacterial candidates and distinguishing between strains in co-cultures. Their facilities in Darlington were impressive, facilitating rapid data generation. We’re now collaborating with CPI again to complete our preclinical program and prepare for the launch of our symbiotic supplement. I am excited to see this hard work translate into improved health for the next generation of infants!

Headshot of Lydia Mapstone, CEO

Lydia Mapstone

CEO

RNAssist

With CPI, we’ve shown that ambient-stable vaccine formulations are achievable, enabling global vaccine equity. CPI’s expertise, including proving the large-scale manufacturability of our TheraPHIX™ stabiliser, has advanced us far faster than we could have managed alone, giving us the credibility to aim for widespread adoption by vaccine manufacturers worldwide.

Headshot of Andrew Goldsborough, CEO

Andrew Goldsborough

CEO

Intract Pharma

Thanks to the expertise in drug development and manufacture brought by the colleagues from Quay, CPI and Pharmidex, we successfully developed a scalable manufacturing process for oral antibody products.

Headshot of Silvia Matiz, Formulation Scientist

Silvia Matiz

Formulation Scientist

AstraZeneca

With digital tools we can build in operational excellence right from the start of pharmaceutical development, improve product robustness, and drive more efficient manufacturing processes to deliver more medicines to more patients, more quickly.

Headshot of Sophie Bailes, Director Digital Transformation

Sophie Bailes

Director Digital Transformation

4basebio

CPI helped us accelerate a vital aspect of our manufacturing process to expedite our journey towards a clinical product. We’ve made significant progress in our GMP manufacturing capabilities, leading to our first DNA sales and increased interest in our products from partners and client base.

Headshot of Carmen Mañas Torres, Team Leader in Synthetic DNA Purification

Carmen Mañas Torres

Team Leader in Synthetic DNA Purification

Immune Boost Clinic

Manufacturing is just one part of the process, and CPI does so much more than just that. Growing mycolicibacteria consistently and reliably to food grade standard and combining them with other ingredients is difficult and requires attention to detail, expertise and experience from your partner.

Headshot of Tim Dye, Senior Scientific and Operations Advisor

Tim Dye

Senior Scientific and Operations Advisor

Trusted by leading organisations

Showing slide 1 of 1
BoobyBiome

CPI was an excellent partner, aiding in demonstrating the manufacturing feasibility of our top bacterial candidates and distinguishing between strains in co-cultures. Their facilities in Darlington were impressive, facilitating rapid data generation. We’re now collaborating with CPI again to complete our preclinical program and prepare for the launch of our symbiotic supplement. I am excited to see this hard work translate into improved health for the next generation of infants!

Headshot of Lydia Mapstone, CEO

Lydia Mapstone

CEO

RNAssist

With CPI, we’ve shown that ambient-stable vaccine formulations are achievable, enabling global vaccine equity. CPI’s expertise, including proving the large-scale manufacturability of our TheraPHIX™ stabiliser, has advanced us far faster than we could have managed alone, giving us the credibility to aim for widespread adoption by vaccine manufacturers worldwide.

Headshot of Andrew Goldsborough, CEO

Andrew Goldsborough

CEO

Intract Pharma

Thanks to the expertise in drug development and manufacture brought by the colleagues from Quay, CPI and Pharmidex, we successfully developed a scalable manufacturing process for oral antibody products.

Headshot of Silvia Matiz, Formulation Scientist

Silvia Matiz

Formulation Scientist

AstraZeneca

With digital tools we can build in operational excellence right from the start of pharmaceutical development, improve product robustness, and drive more efficient manufacturing processes to deliver more medicines to more patients, more quickly.

Headshot of Sophie Bailes, Director Digital Transformation

Sophie Bailes

Director Digital Transformation

4basebio

CPI helped us accelerate a vital aspect of our manufacturing process to expedite our journey towards a clinical product. We’ve made significant progress in our GMP manufacturing capabilities, leading to our first DNA sales and increased interest in our products from partners and client base.

Headshot of Carmen Mañas Torres, Team Leader in Synthetic DNA Purification

Carmen Mañas Torres

Team Leader in Synthetic DNA Purification

Immune Boost Clinic

Manufacturing is just one part of the process, and CPI does so much more than just that. Growing mycolicibacteria consistently and reliably to food grade standard and combining them with other ingredients is difficult and requires attention to detail, expertise and experience from your partner.

Headshot of Tim Dye, Senior Scientific and Operations Advisor

Tim Dye

Senior Scientific and Operations Advisor

Trusted by leading organisations

Showing slide 1 of 1
BoobyBiome

CPI was an excellent partner, aiding in demonstrating the manufacturing feasibility of our top bacterial candidates and distinguishing between strains in co-cultures. Their facilities in Darlington were impressive, facilitating rapid data generation. We’re now collaborating with CPI again to complete our preclinical program and prepare for the launch of our symbiotic supplement. I am excited to see this hard work translate into improved health for the next generation of infants!

Headshot of Lydia Mapstone, CEO

Lydia Mapstone

CEO

RNAssist

With CPI, we’ve shown that ambient-stable vaccine formulations are achievable, enabling global vaccine equity. CPI’s expertise, including proving the large-scale manufacturability of our TheraPHIX™ stabiliser, has advanced us far faster than we could have managed alone, giving us the credibility to aim for widespread adoption by vaccine manufacturers worldwide.

Headshot of Andrew Goldsborough, CEO

Andrew Goldsborough

CEO

Intract Pharma

Thanks to the expertise in drug development and manufacture brought by the colleagues from Quay, CPI and Pharmidex, we successfully developed a scalable manufacturing process for oral antibody products.

Headshot of Silvia Matiz, Formulation Scientist

Silvia Matiz

Formulation Scientist

AstraZeneca

With digital tools we can build in operational excellence right from the start of pharmaceutical development, improve product robustness, and drive more efficient manufacturing processes to deliver more medicines to more patients, more quickly.

Headshot of Sophie Bailes, Director Digital Transformation

Sophie Bailes

Director Digital Transformation

4basebio

CPI helped us accelerate a vital aspect of our manufacturing process to expedite our journey towards a clinical product. We’ve made significant progress in our GMP manufacturing capabilities, leading to our first DNA sales and increased interest in our products from partners and client base.

Headshot of Carmen Mañas Torres, Team Leader in Synthetic DNA Purification

Carmen Mañas Torres

Team Leader in Synthetic DNA Purification

Immune Boost Clinic

Manufacturing is just one part of the process, and CPI does so much more than just that. Growing mycolicibacteria consistently and reliably to food grade standard and combining them with other ingredients is difficult and requires attention to detail, expertise and experience from your partner.

Headshot of Tim Dye, Senior Scientific and Operations Advisor

Tim Dye

Senior Scientific and Operations Advisor

Get in touch

Get in touch

Get in touch