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Accelerate your product to clinical trials.
Upperton’s integrated CDMO services, expertise and nimbleness can accelerate and de-risk your drug program journey.
Talk with our experts in San Diego to see how we can
accelerate and de-risk your journey to clinical trials.
Choose a meeting type from the options below.
Discover unparalleled
project delivery.
We pledge an unwavering commitment to prioritising your project, never relegating it to the bottom of a list. We stand out as a CDMO offering unparalleled service.
Our expansive project team covers every layer of our operations, ensuring a thorough and dedicated science-led approach tailored to your needs.
With extensive experience in steering products from pre-clinical to late-stage manufacture, our Leadership Team form the cornerstone of our service to you, guaranteeing your project benefits from seasoned guidance and hands-on involvement at every stage.
Benefit from a flexible and nimble science-led approach.
With the capability and technology to mirror big CDMOs, our defining traits lie in our adaptability and nimbleness, allowing us to swiftly align with your evolving needs.
As a CDMO like no other, our flexibility ensures we can promptly meet your demands and expectations to accelerate your drug program from formulation development to clinical trial supplies.
Accelerate with our state-of-the-art facility.
Situated in Nottingham, UK, our expansive 50,000 sqft R&D, Analysis, and GMP manufacturing site is the hub for innovation and excellence.
We take pride in offering you seamless scale-up and full-spectrum project delivery, covering the entire journey from pre-clinical stages and formulation development, to late-phase development and analytical services.
Partnering with us means accessing a wealth of knowledge and resources to accelerate your project from inception to realisation.
Achieve your drug program goals
with one integrated CDMO partner.
Talk with our experts in San Diego to see how we can
accelerate and de-risk your journey to clinical trials.
Choose a meeting type from the options below.
Delivering on dosage forms.
Discover more about our dosage forms, techniques and capabilities to support your drug program.
Spray drying
- 0.5g – 5Kg (ProCepT and Niro)
Solvent and aqueous
Micronization
- Up to 1Kg
Dry Granulation
- Up to 4Kg/day (Freund Vector)
- Up to 100Kg / hour (Gerteis)
Blending
- Up to 30Kg/day (Turbula, Pharmatech)
- Up to 250Kg / day (GEA)
Tablets
- Single tablet (Natoli) or up to 1,000,000 / day (Futorque rotary)
Capsules
- Hand filling (Quantos – 500 / day) or Profil – 2,000 / day
- Semi-automated (Bonapache – 25,000 / day) or Zanassi (350,000 / day)
Coating
- Tablet coating up to 5Kg (O’hara), up to 50Kg / batch
Solutions
- Up to 20L preparation vessels with overhead mixing
Suspensions
- Up to 20L preparation, ultrasonic probe, Silverson mixing
Filling
- Hand filling
- Semi-automated (peristatltic pump)
Packaging & Labelling
- Bottles
- Sachet
- Blister packaging (up to 2,000 units per day)
Talk with our experts in San Diego to see how we can
accelerate and de-risk your journey to clinical trials.
Choose a meeting type from the options below.
Talk with our experts
in San Diego.
With unrivalled project management and a member of our Executive Leadership team on every project. Leverage the expertise of Upperton and discover why we’re a leading CDMO like no other. Book a discovery meeting with us at BIO International, 3-6 June 2024.
Meet us at Bio International.
Our team will be at Bio International on June 3-6, 2024 – San Diego Convention Center, California.
Visit our Stand at the UK Pavilion, where you can talk to Dr. Richard Johnson (Chief Scientific Officer) and Dr. Ian Lafferty (Chief Technical Officer).
If you’re looking to work with a CDMO that can accelerate your drug program to the clinic, then we’re here to help.
Fill in the form to arrange a time to meet our experts at Bio International to discuss your requirements.
Book a discovery meeting.
Meet with our experts, Dr. Ian Lafferty (Chief Technical Officer) and Dr. Richard Johnson (Chief Scientific Officer) to see how we can support accelerating your drug program to the clinic.
Our team can meet you on-site in San Diego on Saturday 1st June, Sunday 2nd June and Monday 3rd June.
If you’re looking to work with a CDMO that can accelerate your drug program, then we’re here to help.
Fill in the form to book an introductory discovery meeting with our experts to discuss your requirements.
Book your place at our San Diego Seminar.
How to De-Risk and Accelerate Your Drug Program to Clinical Trials – Oral and Nasal Dosage Form Development.
- Monday 3rd June 2024
- Double Tree by Hilton
San Diego-Mission Valley - Shutters Theatre Meeting Room
- 12pm – 5pm
This seminar will explore relevant solutions for accelerating nasal and oral clinical dosage form development.
Hosted by Dr Richard Johnson, Chief Scientific Officer at UK-based CDMO, Upperton Pharma Solutions, this seminar will cover formulation platforms, analytical characterisation techniques, and different particle engineering strategies to enhance drug success rates.
Key learning objectives
- Gain insights on strategies for reducing risks during nasal and oral clinical formulation development.
- Review drug product options for early clinical evaluation.
- Understand the potential advantages of spray drying to address solubility or particle engineering challenges.
- Network with other professionals.
- Speak with our experts during an interactive Q&A session.