- Clinical Research Organisation
- Licensing and Commercialisation
- Product Development
- Tax and Regulatory Advisor
Adjutor Healthcare works both locally and internationally, providing team members and skills for your business when and where you need them. We provide a suite of seamless, customized services for the development and commercialization of your prescription medicines and medical devices, including:
- competitive strategic development and product positioning
- market assessment
- management of laboratory, non-clinical and clinical programs
- medical liaison plans and pre-launch activities
- identification and engagement with key decision makers and opinion leaders
- project management
- reimbursement and HTA
- quality management systems
- GMP training
- comprehensive auditing solutions including ISO9001, ISO13485, PIC/s GMP, USFDA-specific audits, GLP and cGCP
- data management and statistics
- medical writing
- regulatory dossier report writing and compilation
- regulatory submission services
- orphan, priority and provisional/conditional, fast track, breakthrough and accelerated approvals
- work-sharing and other specialised submissions such as ACSS and Project Orbis
- local regulatory sponsorship
- sponsor and agent services in Europe, North & South America and Asia
- product launch planning and execution
- office set-up including office fit-out, stocking, staffing and systems
- management of logistics functions (3PL & 4PL)
- customer support and medical information lines
- training of sales teams and medical information personnel
- pharmacovigilance and device-vigilance
- product lifecycle management and reporting
- marketing capability to develop and deliver, clever and compliant, promotional materials
Adjutor Healthcare Pty Ltd is part of a worldwide network that spans 90 countries.
Services in New Zealand are available via subsidiary company Adjutor Healthcare (NZ) Limited.
