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As per available reports about 18 relevant journals, 20 Conferences, 28 workshops are presently dedicated exclusively to Packaging Process and about 5412articles are being published on Packaging Process
Packaging can be defined as an economical means of providing presentation, protection, identification information, containment, convenience and compliance for a product during storage, carriage, display and until the product is consumed. Packaging must provide protection against climatic conditions biological, physical and chemical hazards and must be economical. The package must ensure adequate stability of the product throughout the shelf life. It is enlisted in Good manufacturing practices, Market surveillance of industrial pharmacy, Current GMP Guidelines, Quality Control, Current Regulations and Quality Standards, Healthcare pharmacy
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Scope and Importance:
The external image of the package must not only compliment product confidence, but provide clear and concise product identification and other features included arePackage should provide adequate information related to the contents including legal requirements, route of administration, storage conditions, batch number, expiry date, manufactures name and address and product license number. Package should assist in patient compliance.Package should preferably have an aesthetically acceptable design. The primary packaging consist of those packaging components which have a direct contact with the product (i.e. bottle, cap, cap liner, label etc). The main functions of the primary package are to contain and to restrict any chemical, climatic or biological or occasionally mechanical hazards that may cause or lead to product deterioration. Packaging must also function as a means of drug administrations.
Packaging can be defined as an economical means of providing presentation, protection, identification information, containment, convenience and compliance for a product during storage, carriage, display and until the product is consumed. Packaging must provide protection against climatic conditions biological, physical and chemical hazards and must be economical. The package must ensure adequate stability of the product throughout the shelf life.
The external image of the package must not only compliment product confidence, but provide clear and concise product identification and other features included are:
Package should provide adequate information related to the contents including legal requirements, route of administration, storage conditions, batch number, expiry date, manufactures name and address and product license number.
Package should assist in patient compliance.
Package should preferably have an aesthetically acceptable design.
The primary packaging consist of those packaging components which have a direct contact with the product (i.e. bottle, cap, cap liner, label etc). The main functions of the primary package are to contain and to restrict any chemical, climatic or biological or occasionally mechanical hazards that may cause or lead to product deterioration. Packaging must also function as a means of drug administrations. Factor influencing the choice of package:
It is essential to have a survey about the market, the distribution system, manufacturing facilities and other considerations before selecting the packaging material.
The product:
The physical and chemical characteristics of the drug entity, the excipients, the formulation, route of deterioration of the product, type of patient (baby, child, teenager, adult, elderly, infants etc) must be considered while dealing with the pharmaceutical product. Apart from the properties of drug, package style to attract patient and other legal requirements should also be considered during selection.
The market:
The channel of sale should be considered, i.e. where, when, how and by whom it is to be used or administered (e.g. doctor, dentist, nurse, patients etc), whether for home trade and/ or export. The quantity per package and follow up sale must all be carefully considered during package design and selection.
Manufacturing facilities:
The stability of the manufacturing facilities should be considered due to new package, increased sale, improvements in Good Manufacturing Practice, revised product, new product etc.
Function of packaging:
The various functions of packaging are:
Tamper resistant packaging:
The requirement for tamper –resistant packaging is now one of the major consideration in the development of packaging for pharmaceutical products As defined by the FDA "a tamper –resistant package is one having an indicator or barrier to entry which, if breached or trussing ,can reasonably be expected to provide visible evidence to consumers that tampering has occurred tamper –resistant packaging may involve immediate –container /closure systems or secondary –container /carton systems or any combination thereof intended to provide a visual indication of package integrity when handled in a reasonable manner during manufacture ,distribution ,and retail display ".
The following package configuration have been identified by the FDA as examples of packaging systems that are capable of meeting the requirements of tamper-resistant packaging as defined by FDA regulation
Foil paper or plastic pouches
Market Analysis:
The global market for organic light emitting diodes (OLED) was about $2.1 billion and $2.5 billion in 2013 and 2014, respectively. This market is expected to reach nearly $3.1 billion in 2015 and $9.6 billion in 2020, registering a compound annual growth rate (CAGR) of 25.7% for the period 2015-2020.
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This page was last updated on April 27, 2024