Australian Regulatory Guidelines for Medical Devices (ARGMD): Government Reimbursement, Requirements, Fees and Turnaround Time to Product Approval 2017

Topics

• 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

Who should Attend

• 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