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.
We mmanufacture 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.
Placebo matching is a key aspect of pharmacological research, and we offer extensive, rapid and cost-effective services in the field of placebo manufacturing. We fully understand that if you are looking for a placebo to parallel your product, or designing a trial dose that matches an existing comparator, getting a good match can be challenging.
Sponsors require an end-to-end service that can provide comparator products on a global scale.
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.
At Eramol we understand the importance of primary and secondary packaging for your Study design. We know your patients need effective and safe packaging that is easy to use and understand.
Eramol provides a variety of labelling formats, including Tear-Off labels, Just in Time (JIT) labelling, as well as Multi-Lingual Booklet design & printing.
Eramol provides cost-effective storage and distribution services in line with GMP and GDP guidelines.
Our core operation is in the expert production of clinical trial IMPs.
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.
QP releases ensure that batches are released with the appropriate communications, data and regulations for their destination country.