Packaging

Guidelines on Packaging for Pharmaceutical Products | Part IV

Guidelines on Packaging for Pharmaceutical Products | Part IV

Labelling Throughout manufacturing, a succession of specific outer labels are applied to the container of the medicinal product. The level of processing is indicated by the following words:— quarantine— storage— distribution Specifications for labels for finished drug products are defined in the WHO guidelines on GMP for pharmaceutical products. Written labels on the ... Read More
Guidelines on Packaging for Pharmaceutical Products | Part III

Guidelines on Packaging for Pharmaceutical Products | Part III

Containment The design of high-quality packaging must take into account both the needs of the product and of the manufacturing and distribution system. Protection The packaging must protect the product against all adverse external influences that may affect its quality or potency, such as: Stability For primary packaging, it is ... Read More
Guidelines on Packaging for Pharmaceutical Products | Part II

Guidelines on Packaging for Pharmaceutical Products | Part II

Packaging may be defined as the collection of different components (e.g. bottle, vial, closure, cap, ampoule, blister) which surround the pharmaceutical product from the time of production until its use. The aspects of packaging to be considered include: Packaging materials include printed material employed in the packaging of a pharmaceutical ... Read More
Guidelines on Packaging for Pharmaceutical Products | Part I

Guidelines on Packaging for Pharmaceutical Products | Part I

All medicinal products need to be protected and “consequently need to be packaged in containers that conform to prescribed standards, particularly with respect to the exclusion of moisture and light and the prevention of leaching of extractable substances into the contents and of chemical interaction with the contents. The complexity ... Read More
Batch Production Record in Pharmaceutical Industry

Batch Production Record in Pharmaceutical Industry

Batch production record an important tool in Pharma industry. Always I do believe that, every GMP document in the Pharma industry should be written and reviewed by subject matter experts (SMEs). The insights of the document author and reviewer help in making the document written in logical sense with clear ... Read More