Responsibilities:
- Leads or compiles all materials required in submissions, license renewal and annual registrations.
- Following through diligently with the Product owners and Government Authority in cases of Product rejection or delay to resolve such delays.
- Maintain the validity of the Registered Product list, Import/ license and/or any relevant licenses.
- Directs or performs coordination and preparation of document packages for regulatory submissions from all areas of company.
- Recommends changes for labeling, manufacturing, marketing, and clinical protocol for regulatory compliance.
- Coordinating with other departments related to registration, amendment of approved licenses, promotion materials, and advertisement permission.