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Multi-lingual Booklet

Meeting regulatory needs in multiple languages
Bringing a new drug to market comes with many challenges, not least the need to meet multiple regulatory challenges, in different languages, in different jurisdictions.

Complex independent regulatory requirements often fall within a structured, and in some cases restrictive, framework, and are all part and parcel of a launch into a diversity of territories worldwide.

Eramol provides expert advice on label content and label design to ensure regulatory compliance within each proposed territory.

We work closely with you to ensure that critical information is supplied correctly, with any product that we package, working diligently to ensure complete accuracy.

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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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