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Packaging in Pharma Industry is an extensive, comprehensive and multi-faceted task. From containment and protection to convenience, identification and delivery, packaging’s role in the market cannot be underestimated. It is a means of protecting and preserving items contained within, as well as communicating marketing and regulatory information to consumers. Earlier the requirements of these packaging focused exclusively on preserving the quality of enclosed product, whereas today the packaging occupies a significant portion of the overall food and drugs markets. These are extended to cover criteria such as stability and shelf life; convenience and compliance of product use; prevention of product tampering and counterfeiting; ensuring product safety; and brand identity. These products should be designed in such a way that it gives a soothing impact to the users; also the medicine itself has healing effect, so its packaging should complement its features as well. While there is a drive for customisation within packaging industries, there have been concerns that innovation is being hindered by factors such as budgets and regulation. As the packaging industry continues to develop increasingly sophisticated concepts, industries are starting to embrace innovations in this field to improve patient adherence to drug regimens.
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All dispensed medicinal products will need to be dispensed to the patient in a suitable product container. The function of a container for a medicinal product is to maintain the quality, safety and stability of its contents. Although different pharmaceutical preparations will be packaged in different containers depending on the product type, pharmaceutical packaging can largely be grouped. It is device used for providing protection, presentation, identification, information and convenience for pharmaceuticals product from the moment of production until it is used or administered. Drugs need more care in their packaging than do most other product, because any failure in their packing could result in changes in the drug that lead either to a failure to cure, to illness, to injury or even cause death of patient. It should protect the drug product from physical and chemical damage, and also give protection from mechanical and climatic hazards and microbial contamination. It should provide maximum possible information related to the dosage form, provide special precautions specified for different under schedules. Its area not only helps in creation of wealth, preserving product quality, but also lengthens the shelf life of products. This review provides maximum possible information regarding the materials, additives, tests used for manufacturing of containers and closures.
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