2023 Data Entry Labelling 
Pharmaceutical Technology
MARCH 22, 2023
In the US Drug Quality and Security Act (DSCSA), the FDA mandates that manufacturers and trading partners should have full interoperable electronic track and trace systems in place by November 2023. The aim was to streamline workflows in healthcare facilities by reducing error-prone manual data entry for every customer.
Express Pharma
JUNE 28, 2023
The value of India’s retail pharmaceutical market is estimated to touch $59 billion by the fiscal year 2023, which presents a promising opportunity for retail pharmacies to bolster and strengthen their operations. These systems have helped pharmacists efficiently manage their operations, enabling them to generate more revenue.
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GMPSOP
JUNE 28, 2024
In the five years between 2019 and 2023, the FDA issued the following warning letters, closely related to ineffective deviation investigation. Packaging/labeling/Misbranding: 41 warnings vi. Similarly, the packaging, labeling, and misbranding-related warning letters were the top reasons in 2019. incorrect data entry).
GMPSOP
OCTOBER 28, 2023
– Record or capture all generated raw data directly, promptly, and legibly. – Use traceable data sheets or sequentially numbered notebooks. – Date and sign or initial data entries on the day of entry. Can you create a system that can eliminate all defects from a product? (b)
GMPSOP
APRIL 3, 2023
There are also forms, logs, and registers to keep track of all the little details, as well as product specifications, analytical methods, manufacturing formulae, calculation of raw data and more. Sometime these are labelled as the “hidden factory”. The significance of well-designed GMP documentations is immense.
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