Australian Regulatory Guidelines for Medical Devices (ARGMD): Government Reimbursement, Requirements, Fees and Turnaround Time to Product Approval 2017 2017 covers topics such as:
- Easily navigate pertinent website for specific documents for the application to the authorities
- Keys areas of the legislative instrument dictating regulatory requirements
- Your accountability as an Applicant, Sponsor and Manufacturer for products supplied in Australia
- The Regulatory and Reimbursement landscape, for presentation of the competitive and product comparator market to your sales and marketing team
- Assess and critique documentation intended to be submitted
- The complete submission application pathway for products with all risk classifications
Australian Regulatory Guidelines for Medical Devices (ARGMD): Government Reimbursement, Requirements, Fees and Turnaround Time to Product Approval 2017 2017 brings together:
- Regulatory professionals
- Personnel involved in start-up or in well-established global companies with intentions to market their products in Australia
- Personnel involved in Research and Development
- Compliance professionals
- Document control specialists
- Marketing professionals
