Kit Assembly

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Kit assembly

Complete kit assembly for patient comfort

Eramol provides complete kit assembly, grouping individual items to deliver a finished combined product that contains all the necessary information and components for those important end users in your clinical trials.

We will work with you to determine your specific packaging and kitting needs, and develop a custom solution that is both practical and visually appealing for patients.

Kit assembly offers you cost-savings by combining packaging of medications, product literature, delivery devices, special offers and promotions, or any other specified requests.

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We offer a wide range of customised kitting solutions for pharmaceutical drug products that require packing of multiple components into one self-contained package.

  • Our kitting services include labelling, tray packing and boxing with comprehensive verification inspection to ensure the highest level of quality.
  • Discuss with our experienced design team, who will listen to your needs and develop a kit that best serves your product specifications and end-user requirements.
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Our Other Services

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, 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.

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.

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