Clinical trials
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PhaRA Consulting is an active European regulatory affairs consulting firm specializing in supporting pharmaceutical and biotech companies with EU and BENELUX regulatory strategy and operations. They provide services such as drug development advice, regulatory submissions (including EMA/national scientific advice), orphan drug designation applications, pediatric investigation plans (PIP), clinical trial applications (CTA), marketing authorization applications (MAA), and life cycle management. Their areas of special interest include early phase development and unmet medical needs in infectious disease, immunology/inflammatory disease, oncology/immuno-oncology, and vaccines[1][2][3].
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