QP Auditing | Eramol
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QP Auditing

A full range of QP auditing service

All Eramol QPs are IRCA-trained lead auditors with extensive global experience in auditing the following product types and areas:

  • Chemical & biological Active substances (API)
  • Sterile & Non-sterile Drug Products
  • Biotechnological Drug Products
  • QC Laboratories including Data Integrity Audits
  • ATMP & Radiopharmaceutical Drug Products
  • Packaging & labelling sites
  • Warehousing & Storage sites

Eramol also has several regional third-party approved auditors to provide additional global auditing capacity.

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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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Clinical Packaging

Clinical Packaging

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.

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