Clinical Services

Successful Clinical Studies start with Eramol

The journey to your successful Clinical Study begins with a trusted and reliable partner that can support you at every step. Discover our comprehensive range of clinical services for seamless, end-to-end delivery of your IMP, through our four stages of delivery.



  • Placebo Manufacturing
  • Commercial Drug Procurement
  • Formulation Development
  • Clinical Packaging
  • Labelling Solutions
  • Clinical Storage and Distribution
  • Specialised Clinical Supply Chain Solutions
  • EU and UK Imports
  • EU and UK QP release

Manufacturing

We manufacture non-sterile dosage forms including tablets, capsules & oral liquids within our MHRA-approved UK facility. Manufacturing is carried out in state-of-the-art cleanroom facilities using validated pharmaceutical-grade equipment that can cater for small- or large-scale batch sizes.

Labelling and Packaging

We offer primary and secondary packaging, including bottling, blistering, kit assembly and bespoke cartoning solutions.

Logistics and Specialised Supply Chain Services

Eramol provides IMP import services into the EU and UK from around the world; we provide all regulatory documentation and support in navigating the EU and UK legislative landscape.
We provide global distribution & logistics solutions via a network of approved specialist local depots located in key territories including North & South America, Australasia and South East Asia.

Qualified Person Release

Our QPs provide expert regulatory and supply chain advice tailored to the needs of the client and stage of the project lifecycle. Eramol’s QPs can perform UK and EU batch release for clinical drug products.

Formulation Development

Eramol offers clinical formulation development and manufacturing services to enable you to develop your product and speed up your time to market. We’ll work with you to develop an effective formulation – either in solid tablet, capsule or liquid form – giving you optimal clinical outcomes that can support your product across all clinical trial phases.

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 by integrating advanced isolator technology, closed-system processing, moist heat terminal sterilisation and a full end-to-end clinical supply chain — ensuring your sterile injectable, cartridges and pre filled syringes reach 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.

Clinical Packaging

We recognise that the challenge of acquiring adequate placebos is considerable, whether it be matching a placebo or making an active comparator.

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.

EU & UK QP Release

QP Release is a critical stage in clinical trials: it is the process whereby Qualified Persons (QPs) ensure that a batch of investigative medicinal products (IMPs) that has been manufactured are of a high enough quality that they can be released for use in clinical trials.

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.

EU & UK Importation

Eramol’s manufacturing authorisations include EU and UK importation and can act as the physical site of importation for products manufactured further afield, across the globe.

Commercial Drug Procurement

Sponsors require an end-to-end service that can provide comparator products on a global scale. We understand this requires a full supply chain solution to manage a clinical trial. With vast experience in comparator sourcing, as well as a reliable network of quality suppliers and wholesalers, we have successfully sourced comparator products across all clinical markets, assuring supply for hundreds of clinical studies.

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.

Clinical Supply
Chain Solutions

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

EU & UK QP
Release

Eramol provides the seal of approval.

EU & UK
Importation

Authorised for importation in the EU, UK and beyond.

EU & UK QP
Release

Eramol provides the seal of approval.

Reliable. Proven. Safe. Effective.

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Reliable. Proven. Safe. Effective.

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Speak With Us

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Email

enquiry.uk@eramol.com

Phone

+44 (0) 1293 368080