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9 ways pharmacy technician roles are changing

The Checkup by Singlecare

This includes counting, measuring, and packaging medications, as well as labeling and organizing them for distribution. They may also be involved with medication compounding and assisting with clinical trials, depending on the healthcare setting. RELATED: Ways to prevent common pharmacy errors 7.

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EU antibiotic shortages being monitored by MSSG

European Pharmaceutical Review

In addition, MSSG supports temporary national measures such as unit dose dispensing and compounding. MSSG stresses the importance of transparency in relation to shortages and highlights the need for all stakeholders to communicate in an objective and responsible way to avoid any undue public concern.

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Medication management for people who are visually impaired

The Checkup by Singlecare

Understanding the drug label Much of the information you need to know is printed on the label of your medicine. OTC meds usually have a “Drug Facts” label that lists important information. In addition, prescription drugs may have labels with similar information. Medicines taken by injection should be premeasured.

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What to Keep in Your Integrative Medicine Cabinet

The Thyroid Pharmacist

I started talking to Carter Black, RPh, my compounding pharmacist, about the symptoms I was experiencing, and he suggested that I have my adrenals tested. Follow package instructions. These signals create communication and function within nerves and muscles, as the electrolytes move in or out of cells.

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A Proposal for a Comprehensive Quality Overall Summary

ISPE

Challenges with the Current Module 2 Structure The US FDA published a white paper in 2018 calling for a revision to Module 2 because, “there can be a disconnect between applicants and regulators regarding the communication of quality data and its impact on the assessment. Currently, it takes time and/or communications (e.g.,

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A Proposal for a Comprehensive Quality Overall Summary

ISPE

Challenges with the Current Module 2 Structure The US FDA published a white paper in 2018 calling for a revision to Module 2 because, “there can be a disconnect between applicants and regulators regarding the communication of quality data and its impact on the assessment. Currently, it takes time and/or communications (e.g.,

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Regulatory Landscape for Raw Materials: CMC Considerations

ISPE

With shortages, regulatory complexity is compounded due to differences in submission and data requirements from various regulatory agencies. In this article, the term “raw material” refers to a material used in the manufacturing and packaging of a drug substance (DS) or a drug product (DP). Burke, PhD. 1 September 2022.