Getting ready for QP change in 2022
In 2002, an entirely new set of Qualified Persons (QP) Verifications Requirements came into play, with Eramol fully prepared for this new reality.
We offer QP advice and support to guide you through the QP verification process to ensure regulatory compliance of your EU and UK supply chains and study continuation.
Physical importation or direct to site shipment options are fully supported within Eramol’s physical infrastructure.
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.