Product Portfolio

Our drug delivery portfolio covers pens, including pen needles, pre-filled syringes & auto-injectors. We offer a range of platform products as well as bespoke solutions which are custom made to suit your and your patients’ specific requirements.

Marketed Products

Disposable Auto-injector Concepts

Custom Solutions

These innovative products are designed to meet the needs of both our pharmaceutical partners and their patients. We support through the entire process, from consultation, through to design and taking the product to market.



We listen to your needs to determine the best solution, drawing on our experience of multiple primary containers, formulations and therapies. From simple rebrands of an existing technology to wholly bespoke designs – we can help you achieve your goals.

Owen Mumford Consultation
Owen Mumford Design


A multi-disciplinary team of professionally qualified experts ensures that design concepts meet your exact requirements. The thorough understanding of your end users’ needs includes the incorporation of human factors and ergonomics studies.



A close collaboration between design, production and your own team will ensure your device is designed for manufacture while still keeping patient satisfaction in mind.

Owen Mumford Develop
Owen Mumford Delivery


The production of your device is tailored to your needs – from low-volume hand assembly to high-volume automation. We are also licensed for the final assembly of combination products.


Continuous improvement

As markets, regulations and formulations change, your device requirements can evolve. Through continuous improvement, we can help ensure these needs are met.


Quality & regulatory


Your device plays an integral role in people’s lives, and every associate at Owen Mumford bears responsibility for the quality of our products. The Quality team maintains the quality ethos and operates independently from manufacturing, development, and sales to achieve true objectivity.

Thanks to our design and build capability, your project is subject to the same quality management system throughout its development – and into production. This assures greater consistency and potentially fewer complications than more fragmented approaches.

Product testing guarantees the quality of your device, and is implemented from your first prototype, throughout its development, and during production. This includes material testing, usability engineering, full process validation, benchmark testing and in-line functional testing

Rest assured that we are fully accredited, and our processes are compliant with all relevant standards.

Accreditation and standards

  • We adhere to all relevant international standardisation guidelines, including:
  • International Organisation for Standardisation ISO 13485.2003
  • Medical Device Directive MDD 9342EEC Annex II
  • Annex V, Food & Drug Administration (FDA) CFR 21 section 820 Part 11
  • CMDCAS 13485 Canadian Health Authority

Regulatory submissions

Regulatory submissions can sometimes feel daunting. We see it as part of our job to help you navigate through this process.

Your product will be developed and manufactured in accordance with all applicable regulatory guidelines. We carefully establish and maintain Design History Files, the Device Master Record, the Technical file, and provide Risk Management Files.

With decades of experience in regulatory submissions, we can if needed, assist with regulatory strategy and submissions. This can include technical files under the Medical Device Directive 93/42/EEC and FDA 510(k).

Due diligence

Our locations are audited and inspected multiple times each year, and our customers are also welcome to inspect our premises. We have an excellent compliance record for ISO 13485 requirements, and our quality team continually helps drive improvements, which is beneficial for both you and your end users.

Post-launch support

After launch, a dedicated account manager will work with you to ensure your on-going needs are satisfied and to ensure that good communication continues. By collecting feedback from end users, our corporate partners, medical professionals, and trade associations, we are always aware of the latest market changes. We can help you find unique ways to market your product as well as help you continually innovate and improve. This may include evolving a successful device to meet your changing needs or planning a next generation solution.

We take partnerships seriously. From packaging through production, we are with you all the way.

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