Our translators’ team consists of both in-house translators and external translators with medicinal or linguistic education respectively. PharmDedict always liaise with end-clients and perform proof-reading at all stages to ensure all translations are complete and comply with the current EMA QRD requirements or other relevant requirements. We may support you with:

–  Translation of Product Information;

–  Translation of related registration documentation:

Quality, Clinical and Non-clinical overviews and summaries;

Standard Operating Procedures;

Validation documentation;

Batch Manufacturing Records;

–  Medical and Scientific papers and articles;

–  All kinds of legal texts and contracts;

–  Trademark documents;

–  Patents and patent disputes;

–  State decrees and regulations.