My first trip away from my home was to see my son Stirling, whom I haven’t seen in over eighteen months, in Washington State. I choose to take McKay’s book to read on the trip.Â
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Marketing and/or manufacturing authorisation holders are obliged to report to EMA if they detect any (suspected) falsification of a centrally authorised medicine that could pose a risk to public and animal health. For more information and full instructions, see:
Once implemented, patients will be able to check whether the medicines they purchase are genuine through a text message to a number provided on the labels by companies marketing the drug.
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Falsified medicines do derece pass through the usual evaluation of quality, safety and efficacy that is required for the EU authorisation procedure. Because of this, they sevimli be a health threat.
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may not meet the same standards of quality, safety and efficacy as those approved by the TGA for supply in Australia.
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These pharmaceutical manufacturing changes have created record-keeping challenges and medication quality concerns. The contaminated blood pressure medication
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