Using Cold-Stage MDRS to Study Temperature-Driven Particle Changes in Nasal Spray APIs Using Cold-Stage MDRS to Study Temperature-Driven Particle Changes in Nasal Spray APIs Read More »
The use of Antimicrobial Effectiveness Testing in Pharmaceutical Microbiology The use of Antimicrobial Effectiveness Testing in Pharmaceutical Microbiology Read More »
Understanding Paper-Film Sterilisation Pouches: A Practical Guide for Healthcare Settings Understanding Paper-Film Sterilisation Pouches: A Practical Guide for Healthcare Settings Read More »
ISO 18562-3:2024 Carbonyl Testing Requirements and What Manufacturers Need to Know ISO 18562-3:2024 Carbonyl Testing Requirements and What Manufacturers Need to Know Read More »
Chemical Characterisation in Medical Devices: Improved Extractables and Leachables Testing with PAL3 Series II Technology Chemical Characterisation in Medical Devices: Improved Extractables and Leachables Testing with PAL3 Series II Technology Read More »
USP <382> Update: What Manufacturers Need to Know for Functional Suitability of Elastomeric Components USP <382> Update: What Manufacturers Need to Know for Functional Suitability of Elastomeric Components Read More »
Extractables and Leachables Testing for Pre-Filled Syringes Extractables and Leachables Testing for Pre-Filled Syringes Read More »
White Paper: Optimising X-Ray Diffraction for Challenging Pharmaceutical Sample Types White Paper: Optimising X-Ray Diffraction for Challenging Pharmaceutical Sample Types Read More »
Meet the Physical Characterisation Team at Cormica Bradford Meet the Physical Characterisation Team at Cormica Bradford Read More »
ASTM F623-25: Key Updates to the Foley Catheter Performance Standard ASTM F623-25: Key Updates to the Foley Catheter Performance Standard Read More »
Adapting to ISO 10993-1: Strategic Considerations for Device Developers​ Adapting to ISO 10993-1: Strategic Considerations for Device Developers​ Read More »
ISO 8871-5:2025 – Revised Testing for Injectable Components ISO 8871-5:2025 – Revised Testing for Injectable Components Read More »
ISO 10993-23: Expanded In Vitro Methods for Skin Irritation ISO 10993-23: Expanded In Vitro Methods for Skin Irritation Read More »
Why Every Medical Device Manufacturer Needs a Solid Biological Evaluation Plan (BEP) Why Every Medical Device Manufacturer Needs a Solid Biological Evaluation Plan (BEP) Read More »
Delivering Confidence in Respiratory Testing: Cormica’s View from RDD 2025​ Delivering Confidence in Respiratory Testing: Cormica’s View from RDD 2025​ Read More »
