The packaging requirements of the pharmaceutical industry are specific and complex, as they play a central role in the protection and quality assurance of medicines. The requirements for pharmaceutical packaging are regulated on several levels in order to guarantee the efficacy, safety and stability of the products.
Quality and stability:
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- Protection from environmental influences: Medicines must be protected from moisture, light, oxygen and temperature fluctuations in order to maintain their stability and efficacy.
- Conformity with regulations: Packaging must comply with the regulations and standards of health authorities such as the FDA (USA) or EMA (EU).
- Sterility: Packaging must ensure sterile conditions, especially for injectables or infusions.
- Durability: The packaging should ensure the shelf life of the product over its entire life cycle.
Transport and storage requirements:
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- Temperature resistance: Packaging must be able to withstand extreme temperatures, both hot and cold, without losing integrity.
- Stackability and space utilisation: Efficient space utilisation and stable stackability are crucial for storage and transport.
- Transportability: The packaging must ensure safe transport and storage, even under extreme conditions.
Handling and ease of use:
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- Dosing systems: Simple and precise dosing systems are important to ensure the safe and accurate application of chemicals.
Our following products are suitable for these requirements:
Fluid bag on a discharging machine
