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Services

Since our establishment, Plunkett Consulting Group has grown to utilise its key asset, our people, to provide high quality and effective support to our clients. Our focus is in two key areas within Pharmaceutical and Medical Device field: Regulatory Affairs and Clinical Development.

Through our collaboration with local and international partners, Plunkett Consulting Group can provide additional services to support our clients’ needs.

OUR EXPERIENCE

Australian device approvals

Category 1 Applications

ODD Submissions

TGA Meetings

CTN submissions

Clinical Trial sites

Dossiers reviewed

IND/IDE Submissions