Cormica’s global laboratories partners with pharmaceutical and medical device manufacturers to offer expert testing solutions and regulatory expertise to help you navigate the complexities of release a product. Cormica, operates under strict GMP, GLP, and ISO 17025 accreditations, demonstrating our unwavering commitment to data integrity and quality.
Physical & Packaging Testing: We validate product functionality, durability, packaging integrity, and safe transport through a suite of tests tailored to medical devices and regulatory standards (ISO, ASTM, ISTA).
Microbiology & Environmental Monitoring: We ensure the sterility and microbial safety of your products and manufacturing environments with specialized testing, including bioburden, sterility, endotoxin testing, and cleanroom monitoring.
Analytical Chemistry: We analyze materials, formulations, and device components with a wide range of techniques to support your development, quality control, and regulatory submissions. Comprehensive materials characterisation techniques and applications including Particle Size Analysis.
We offer a streamlined testing experience, from early-stage material analysis and prototyping support through final product release and post-market surveillance.
GMP | GLP | ISO 17025