Delivering tomorrow's medicine today​

A bespoke clinical trial manufacturing service, driven by quality.

ABOUT US

Power Up with Eramol

Founded in 2013, Eramol is a quality-driven CMO established by Qualified Persons, built from the ground up with regulatory excellence at its core. Quality is not a function at Eramol, it is the foundation of how we operate.
 
We provide end-to-end services across both sterile and non-sterile manufacturing, supporting clients from early clinical development through to commercial manufacture and global distribution. Holding both clinical and commercial manufacturing authorisations, we enable seamless progression across development phases, helping sponsors reduce complexity to accelerate time to market.
 
Eramol is privately owned and independent, allowing us to act decisively and always in the best interests of our clients. This independence underpins our client-centric approach, enabling flexibility, responsiveness, and innovation without compromise.
 
Every project at Eramol is QP-led. Dedicated Qualified Persons are assigned to each programme, providing direct access, clear accountability, and proactive regulatory oversight throughout the product lifecycle. This close, transparent working model ensures informed decision-making, risk mitigation, and consistent delivery.
 
With bespoke capabilities, rapid turnaround times, and a strong quality culture, Eramol is a trusted partner for clinical trial supply and commercial manufacturing in the UK, across Europe, and worldwide.
Tailored Solutions
Customer Focused
Flexible Approach
Global
Presence

Targeted Science. Real
Impact. Better Lives.

Discover a wider range of specialised pharmaceutical solutions designed to support every stage of your workflow.
From research to delivery, we provide the expertise and reliability you can trust.

Sterile Manufacturing

Eramol delivers a purpose-built, EU GMP Annex 1–compliant sterile manufacturing service dedicated to Phase I and Phase II clinical trial supply. Our facility is designed for agility, reliability, and regulatory strength, integrating advanced isolator technology, closed-system processing, moist heat terminal sterilisation, and a full end-to-end clinical supply chain — ensuring your sterile injectable reaches patients safely, on time, and in full regulatory compliance.

Non Sterile Manufacturing

GMP Production of Tablets, Capsules & Oral Liquids for Phase I–III and Commercial Supply Eramol delivers end-to-end non-sterile manufacturing built on a foundation of quality, regulatory expertise, and Qualified Person (QP) leadership. Our Sevenoaks GMP facility, commissioned in November 2021 and operational since August 2022, supports the full product lifecycle—from early-phase clinical development right through to commercial supply.

Labelling Solutions

Our versatile and extensive labelling solutions have been designed to offer flexibility, economy of scale and to meet the demands of last-minute requirements.

Clinical Storage & Distribution

Eramol provides cost-effective storage and distribution services in line with GMP and GDP guidelines. Pharmaceutical storage and the distribution of clinical trial materials enable us to provide key logistics support to our clients worldwide.

Formulation
Development

Providing the formulae for success to support your product across all clinical trial phases.

Clinical
Packaging

Eramol provides optimum packaging for ultimate outcomes.

Clinical Storage
& Distribution

Logistics management for safe storage and efficient distribution.

Clinical Supply
Chain Solutions

Developed to meet the exacting standards of our clients and country specific compliance and regulatory standards.

EU & UK
Importation

Authorised for importation in the EU, UK and beyond.

EU & UK QP
Release

Eramol provides the seal of approval.
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Why Partner with Eramol?

  • Fully integrated end-to-end services from manufacture to patient
  • QP-led quality and regulatory oversight for every project with combined over 40 years QP experience
  • Agile, client-focused project management for rapid and seamless execution
  • Trusted partner for global clinical and commercial supply chains
  • Expertise in both sterile and non-sterile manufacturing, clinical packaging, labelling, and distribution

A bespoke clinical trial manufacturing service, driven by quality.



Eramol is perfectly positioned and proud to support your bespoke manufacturing requirements that enable better healthcare for the world. We are as passionate about your success as you are.

Eramol was founded in the UK by two Qualified Persons, with a shared vision to offer high quality, end-to-end manufacturing & global distribution services for clinical trials for commercial and non-commercial clients.

That vision is today a successful reality, and we are renowned for serving international pharmaceutical companies and research organisations over the world.

A full-service operation, created to meet your needs.

We understand the benefits of a one-stop-shop for clinical trial supply service. We cover the full spectrum of your needs and cater for both small- and large-scale batch manufacturing in our state-of-the-art MHRA & HPRA approved facilities.

QP release, direct to patient supply & global distribution is provided via our UK and EU facilities:

Every step of our comprehensive and dedicated clinical service is the result of specialist industry knowledge and over 30 years’ innovation in the pharmacological development sector.

SERVICES

Solutions Designed for You

At Eramol, we deliver end-to-end pharmaceutical support through a comprehensive suite of services designed to ensure quality, reliability, and efficiency at every stage. Our Clinical Services provide structured, compliant solutions to support research and healthcare needs. With Placebo Manufacturing, we offer precise, controlled formulations tailored for clinical trials and product testing. Our Labelling Solutions ensure accuracy, clarity, and regulatory compliance for all product types. Additionally, our Commercial Drug Procurement service enables seamless access to high-quality medicines through trusted sourcing and streamlined supply chains—making Eramol a complete partner in healthcare excellence.

Clinical Services

Our Clinical Services are designed to support every stage of research with precision, compliance, and scientific integrity. We provide tailored solutions that assist in planning, managing, and executing clinical studies with the highest standards of safety and quality. From protocol development and documentation support to sample handling and trial coordination, our team ensures seamless operations backed by regulatory expertise. With a focus on accuracy, transparency, and dependable delivery, we help research teams achieve reliable outcomes and accelerate the journey from concept to clinical success.

Our Clinical Services are designed to support every stage of research with precision, compliance, and scientific integrity. We provide tailored solutions that assist in planning, managing, and executing clinical studies with the highest standards of safety and quality. From protocol development and documentation support to sample handling and trial coordination, our team ensures seamless operations backed by regulatory expertise. With a focus on accuracy, transparency, and dependable delivery, we help research teams achieve reliable outcomes and accelerate the journey from concept to clinical success.

Our Clinical Services are designed to support every stage of research with precision, compliance, and scientific integrity. We provide tailored solutions that assist in planning, managing, and executing clinical studies with the highest standards of safety and quality. From protocol development and documentation support to sample handling and trial coordination, our team ensures seamless operations backed by regulatory expertise. With a focus on accuracy, transparency, and dependable delivery, we help research teams achieve reliable outcomes and accelerate the journey from concept to clinical success.

Our Clinical Services are designed to support every stage of research with precision, compliance, and scientific integrity. We provide tailored solutions that assist in planning, managing, and executing clinical studies with the highest standards of safety and quality. From protocol development and documentation support to sample handling and trial coordination, our team ensures seamless operations backed by regulatory expertise. With a focus on accuracy, transparency, and dependable delivery, we help research teams achieve reliable outcomes and accelerate the journey from concept to clinical success.

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