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.
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.