Sterifast Medical Packaging Validation Laboratory

 

At Sterifast, we ensure that medical packaging meets the highest standards of safety and compliance. Our Medical Packaging Validation Laboratory operates in full accordance with ISO 11607 and the quality system regulation, guaranteeing reliable, high-quality validation services. Additionally, we comply with ISO/IEC 17025, ensuring accurate testing and calibration.

Our Expertise Includes:

✔ Material, Process & Equipment Qualification – Ensuring optimal performance and compliance.
✔ Accelerated Aging – Simulating real-world conditions to evaluate product durability.
✔ Barrier Properties Testing – Assessing material resistance against microbial penetration.
✔ Seal & Tensile Strength Testing – Validating the integrity and durability of seals.
✔ Installation, Operational & Performance Qualification (IQ, OQ, PQ) – Verifying the efficiency of sterilization and packaging processes.
✔ Mechanical Properties Testing – Evaluating material strength, flexibility, and reliability.

Our state-of-the-art laboratory plays a crucial role in sterile medical packaging validation, ensuring that your products comply with international regulations and remain safe and effective throughout their lifecycle.