The requirements are particularly high, as they must safeguard sensitive products during both transport and storage. Factors such as mechanical durability, temperature resistance, moisture protection, and chemical stability play a crucial role.
Highly sensitive equipment, such as sterile instruments or diagnostic kits, require shock-absorbing components to prevent damage. Another key factor is the sealing process, which prevents the intrusion of moisture, air, or contaminants.
Climatic conditions also present a challenge. These protective layers must be designed to withstand temperature fluctuations without deforming or losing their protective function. Specialized barrier layers shield against UV radiation and oxygen exposure, which is particularly important for pharmaceutical products.
Strict regulations apply to the storage. The packaging must ensure the durability of the contained products by preventing contact with moisture, dust, or microorganisms. Especially for sterile products, airtight containment systems are necessary to eliminate long-term contamination risks.
ISO 10993 sets specific standards for biocompatibility used in storage. Certified components guarantee that no harmful interactions occur with the products inside. The choice of components is also critical: cardboard, paper, and flexible films must not only be stable but also easy to open for safe handling in medical environments.
Manufacturers increasingly rely on advanced packaging solutions with antibacterial coatings or biodegradable alternatives. These innovative approaches not only enhance protection during transport and storage but also reduce environmental impact.
By combining mechanical stability, sterile protection, and sustainable development, modern containment methods meet high standards and guarantee safe usage in medical applications.