Acadustri provides expert medical writing services to support all stages of your product’s life cycle.
Our industry experience and extensive medical writing credentials mean we are ideally placed to offer authoritative guidance on document content and structure, in addition to end-to-end writing for all stages of drug development.

It also provide Pharmacovigilance medical writing that plays a crucial role at every stage of the drug development process.

Our writing skills and industry expertise ensure Acadustri can provide the support and guidance needed to prepare clinical and regulatory documents:

Clinical Study Reports for phase I-IV trials to ICH guidelines
Investigator's Brochures
Study Protocols & Protocol Amendments
INDs & NDAs in CTD formats
‘Response to Questions’ Documents
Investigational Medicinal Product Dossiers
Literature searches/reviews

As a specialist service provider in this area, we continue to provide leadership, plus content writing and guidance on report structure, to existing and new clients wherever needed, and have a full and broad understanding of all necessary requirements for all types of safety reports.

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