Cormica's Services
Comprehensive Testing Services for Global Compliance
Cormica delivers trusted pharmaceutical, medical device, and combination product testing services that meet the highest regulatory standards worldwide. With GMP, GLP and ISO 17025 accredited laboratories across the UK, EU and US, we support product development, validation, release and post-market surveillance.
Our integrated solutions ensure rapid, reliable results aligned with ICH, USP, EP, JP, FDA, ISO 10993 and MDR requirements.
Pharmaceutical Testing Services
Cormica offers full suite of pharmaceutical testing for active pharmaceutical ingredients (APIs), excipients, and finished products. Our team supports method development, validation and GMP batch release across clinical and commercial phases. We also provide accelerated and long-term stability testing and complex generic development, including IVBE studies.
Services Include:
- Chemical method development & validation (chromatography, spectroscopy, elemental analysis)
- Microbiological method development (bioburden, sterility, PET/AET, endotoxins)
- GMP release testing
- Extractables & leachables (E&L)
- Stability studies (ICH conditions)
- Physico-chemical analysis
- Generic & complex product support
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Medical Device Testing Services
Our medical device testing capabilities are designed for global compliance with ISO, FDA and MDR standards. From sterility and biocompatibility to packaging validation and functional performance, we help you navigate device submissions with confidence. As combination products continue to grow, our integrated approach ensures both pharmaceutical and device components are tested to regulatory expectations.
Services Include:
- Biocompatibility testing (ISO 10993)
- Microbial quality & sterility (USP, ISO)
- Packaging validation (ISO 11607, ASTM)
- Device performance testing (ISO 11040, ISO 80369)
- Combination product characterisation
- Environmental monitoring & endotoxin testing
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