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Supply chain assessments

Assessing the surety of the most complex Supply Chains

Creating a unique medical solution and planning for its successful roll-out in clinical trials is a complex process – particularly when the scope of implementation is international.

Eramol provides specialist advice in this area, undertaking prospective risk assessments for end-to-end supply chains. We detail key aspects of a project such as its sustainability, together with contingency planning assessments in the event of supply and distribution complications.

We can illustrate local depot or direct-to-site distribution models, factoring in local regulatory and customs requirements for each proposed territory.

Getting your medicinal supplies manufactured and distributed across the world takes time, planning and a considered budget. Eramol ensures that all factors are addressed, leaving nothing to chance in local, and international, supply chains.

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Placebo manufacturing

Placebo manufacturing

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.

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EU & UK Importation

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.

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EU & UK QP Release

EU & UK QP Release

QP releases ensure that batches are released with the appropriate communications, data and regulations for their destination country.

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