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GMP

Draft Quality Review of Documents recommendations on pack design and labelling for centrally authorised non-prescription human medicinal products

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Effective Date
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Filename
draft-quality-review-documents-recommendations-pack-design-and-labelling-centrally-authorised-non-prescription-human-medicinal-products_en.pdf
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078d2ea3861d426c6459687693cfcfc58f15ee5a5672ea7c27102f4d9f70d550

Change Summary

Imported from European Medicines Agency source page.

Version Change Structure

1) Rationale for the change

Not specified for this version.

2) To whom it applies

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4) The current change description

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