Nadiah Adam Email & Phone Number

1. Strategize and execute registration planning for Biomed Global’s group of companies in Singapore and Myanmar, aiming for shortest timeline for market access while maintaining compliance for various range of medical devices (GMD and IVD).2. Provide advice to internal and external stakeholders on various regulatory matters to ensure compliance to applicable regulatory requirements.3. Provide assessment on product's Change Notification and ensuring the application is submitted within the specified timeline.4. Reviewing and submitting Field Safety Corrective Action reports and adverse event reports to local competent authority.5. Handling various tasks with regards to other Regulatory Agencies in Singapore such as NEA, SCDF and IMDA.6. Provide support in maintaining the company's Quality Management System (ISO 13485, ISO 9001 & GDPMDS), with implementations of applicable policies and processes.7. Assisting and participating in company's internal and external audits. Qualified internal auditor for ISO 13485.

Kuala Lumpur, Malaysia

1. Supported international registrations in the APAC region (Singapore, Indonesia, Thailand, Vietnam, Myanmar, South Korea and Taiwan) for SCHILLER group portfolio products.2. Completed product registration with MDA within 6 months including CAB stage with complete documentation.3. Reviewed, planned and submit SIRIM registration for medical devices with communication module.4. Compiling information regarding product's Change Notification and notifying competent authorities and distributors accordingly.5. Preparing and submitting Field Safety Corrective Action reports and adverse event reports to local competent authority.6. Assisting in maintaining the company's Quality Management System (ISO 13485, ISO 9001 & GDPMD), with revisions and implementations of new policies and processes. Successfully implemented transition of hardcopy QMS documents to softcopy documents with minimal cost in order to be in line with environmental friendly approach.7. Providing continuous awareness education to internal staff in order to comply with regulatory standards and requirements.8. Assisting and participating in company's internal and external audits.

Kuala Lumpur, Malaysia

1. Manage and coordinate a team of 6 members to ensure timely content update, complaint or feedback handling, and other related topics for the resource portal.2. Developed and implemented process flow to outline the resource portal management procedures. Ensure that the process flow is communicated well to team members.3. Conduct fixed interval meetings amongst team members to discuss issues relevant to the resource portal and report to the management.4. Ensure that all content updates are verified by the HOD and recorded accordingly.

1. Trained and specialized in Intensive Care Unit (ICU), Neonatal Intensive Care Unit (NICU) & Transport Ventilators.2. Provide continuous training and educations to medical staffs through lectures, presentations & demonstrations to ensure that they are fully well-versed with the equipment.3. Experienced in pre-sales/ post-sales demonstration and presentation.4. Experienced in introducing new ventilator brands to the market & successfully securing sales while working closely with Sales Department.5. Responsible for the completion of ventilator tender specifications for government or private hospitals.

South Korea

1. Worked on fabricating improved X-ray conversion films for radiography detectors. 2. Worked on assessing wrist motion via electromyography (EMG) and MATLAB analysis. 3. Assisted local Biomedical research team in assigned task.