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Can holograms help in the frontline fight against pharmaceutical counterfeiting?

European Pharmaceutical Review

One area in which the problem can be tackled effectively is product packaging. With predictions that the global market for anticounterfeiting packaging is set to reach almost $250 billion by 2026, growth in authentication and anti-tamper devices such as holograms appear to have a healthy future.”

Packaging 111
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Can you drink on Mucinex?

The Checkup by Singlecare

Always follow the directions on the packaging or consult a healthcare professional if you have concerns about the appropriate dosage. Signs of misusing dextromethorphan may involve taking the medication in amounts higher than the recommended dosages or using them for non-medical reasons, such as to feel euphoria.

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CoQ10 side effects and how to avoid them

The Checkup by Singlecare

CoQ10 comes in dosage strengths of 30 mg to 600 mg. Use the suggested dose on the packaging, but it may be advisable to start with the lowest possible dose. Taking large doses of CoQ10 (over 100 mg per day) may not be worth it unless the dosage is prescribed by a doctor. Take the suggested dose. Do not overdo it.

FDA 52
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Contamination Trends & Proposed Solutions

ISPE

The cases covered the same types of contaminants and impurities noted in Table 1: microbial contaminants, process-related im-purities, metal contaminants, packaging-related contaminants, drug cross-contamination, and an “unknown” category encompassing other contaminants associated with the manufacturing process, including those from cell culturing.

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A Proposal for a Comprehensive Quality Overall Summary

ISPE

As part of the US Food and Drug Administration (FDA) QbD pilot 4 in 2005–2006, the need to convey how the control strategy is linked to the target product profile (TPP) and quality target product profile (QTPP) was discussed. 2005N–0262) Federal Register (2005). Published November 2005. 5 Bangemann, M.

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A Proposal for a Comprehensive Quality Overall Summary

ISPE

As part of the US Food and Drug Administration (FDA) QbD pilot 4 in 2005–2006, the need to convey how the control strategy is linked to the target product profile (TPP) and quality target product profile (QTPP) was discussed. 2005N–0262) Federal Register (2005). Published November 2005. 5 Bangemann, M.

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CMC Requirements for New Drug Registration in Latin America

ISPE

In addition to the COR, some Latin American markets require approval in the COO, which is defined as the country where the drug is manufactured, packaged, or exported from. Sometimes, COAs for the drug substance, the excipients used in the formulation, and the primary and nonfunctional secondary packaging material are requested.