labelling and packaging of drug
Drug labelling and packaging represents a critical component in pharmaceutical manufacturing, serving multiple essential functions in ensuring medication safety and compliance. This process encompasses the design, production, and implementation of both primary and secondary packaging materials, along with accurate labelling that provides crucial information about the drug. Modern drug packaging systems incorporate advanced technologies such as tamper-evident features, child-resistant mechanisms, and smart packaging elements that can monitor environmental conditions. The primary functions include protecting the drug from external factors like light, moisture, and temperature variations, maintaining product integrity throughout its shelf life, and providing essential information about dosage, storage requirements, and safety precautions. The technology involved ranges from basic blister packs to sophisticated track-and-trace systems using RFID and serialization. Additionally, the packaging must comply with stringent regulatory requirements while ensuring patient compliance through clear instructions and proper identification of the medication. The application of these systems extends across various pharmaceutical sectors, from over-the-counter medications to prescription drugs, with specific considerations for different drug forms including tablets, liquids, and biologics.