Pharmaceutical Consultant, Qualified Person - Romania

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simona.stanescu
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I’m able to provide QP services for pharmaceutical companies in accordance with Directive 2001/83/EC on a daily or weekly basis.

Writing documentation including Technical Files, Design CTD Dossiers, manuals, forms, templates, creation and review of package leaflets, procedures etc as required for regulatory compliance of Customer's products.

Regularly provide quality management system audit or gap assessments and then set about closing the gap.