Partnerships

The missing link in your business

Few businesses can achieve everything they want to without some behind-the-scenes support.

A lean-running business needs to focus on building its markets and customer base, not on the admin. Outsourcing your back office function can help you do just that.

We have the people and the expertise to save you from getting bogged down in paperwork, HR issues, book-keeping, accounting and compliance. And because we know the medical and pharmaceutical sector like the back of our hand, we can help with problems that might challenge a non-specialist.

For example:

  • We’ve helped a client ensure compliance with the Falsified Medicines Directive (FMD)
  • We are implementing processes to ensure traceability to meet the requirements of the Medical Device Regulations (MDR) for our EU supply chain
  • We’re continuously improving. We’ve been ISO9001-accredited for over 10 years, with consistently successful audit outcomes.

Most of our clients stay with us for years, decades even. We’ve provided back-office support for over 30 years to a market leader in medical devices, for instance.

How we can help

Distribution

Complete supply chain management including import and export, from a central location with good links to major routes.

Compliance

Over 50 years’ experience in pharma and medical device quality management, including complaint management, post-market surveillance, non-conformance reporting, supplier management.

Document management

Managed Microsoft Office 365 services to maintain your documents wherever you are in the world.

Authorised representative

We can represent you in registering your product in the UK, with dossier management and oversight of the regulatory requirements of post-marketing surveillance.

Looking for partnership services? Get in touch.  

Our Expertise

FMD

Supported our partner with the implementation of systems to ensure compliance with Falsified Medicines Directive (FMD) introduced in 2019

MDR

Implementing processes to ensure traceability to meet the requirements of Medical Device Regulations (MDR) for our EU supply chain

ISO9001

Accredited for over 10 years, with consistently successful audit outcomes. Continuously seeking opportunities for improvement