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RFID: The future of smart labelling?

Pharmaceutical Technology

In August of 2022, Fresenius Kabi announced a three-year plan to add GS1 Data Matrix barcodes, also known as 2D barcodes, to its US pharmaceutical portfolio. The aim was to streamline workflows in healthcare facilities by reducing error-prone manual data entry for every customer.

Labelling 105
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Why intelligent automation is the future for regulation

pharmaphorum

To improve data confidence regulatory executives should take a four-step approach to change how they: Collect Data: Life sciences organisations should utilise cloud-based solutions with global access that facilitates one repository with a single source of truth and eliminates the use of local file sharing and servers.

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How is digital technology helping Indian pharmacists

Express Pharma

Features such as updating store inventory details by uploading purchase bills significantly reduce the time in data entry, allowing pharmacists to focus on more complex work. Other related technologies such as scanning barcode labels on packages have also facilitated electronic purchasing and procurement on a larger scale.

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Preparing for an Inspection or Accreditation Survey – Part 2

National Association of Boards of Pharmacy

Then, walk through each step of the practice of pharmacy such as data entry; drug utilization review; compounding; final association between the drug, the prescription, and the label (eg, the dispensing act); and patient counseling.

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Advancement through adversity: how Covid-driven innovations are becoming best practices for pharmacovigilance

Pharmaceutical Technology

AEs can be caused by using medicinal products within or outside the terms of their marketing authorisations (such as off-label therapeutic use, overdose, misuse, abuse or medication errors), as well as from occupational exposure.

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What are the elements of quality control process in pharmaceuticals

GMPSOP

– 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. – Archive records so that they are protected, secured, and easily retrievable.

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Deviation investigation guidelines in the pharmaceutical industry

GMPSOP

Packaging/labeling/Misbranding: 41 warnings vi. Similarly, the packaging, labeling, and misbranding-related warning letters were the top reasons in 2019. incorrect data entry). This is a critical deviation since the medicinal batch does not comply with the label claim (strength) and violates regulatory expectations.