fas fa-search
INVITATION TO PROFICIENCY TRAINING FOR NEW CAB PERSONNEL
PRE-MARKET CONTROL DIVISION (BKPP)
MEDICAL DEVICE AUTHORITY (MDA)
Greetings from the Authority,
INVITATION TO PROFICIENCY TRAINING FOR NEW CAB PERSONNEL
The above stated subject is referred.
2. As potential personnel associated with Conformity Assessment Bodies (CABs) or Medical Device Establishments within the medical device sector, we are pleased to extend an invitation to participate in the upcoming Proficiency Training for New CAB Personnel which will be organized physically, as per the details below:
2.1 Training Details
Dates: February 26, 2024 (Monday) to February 29, 2024 (Thursday)
Venue: Putrajaya International Convention Center (PICC), Putrajaya
Registration Form: Online Registration Form
Registration Deadline: February 19, 2024 (Monday)
Training Courses: Proficiency Training Syllabus
2.2 Eligibility Criteria
To attend the upcoming training, participants must have never attended any proficiency training previously, be currently employed as internal/external auditors, technical personnel, regulatory affairs, or any individuals within the medical device sector, and meet other specific criteria, including individuals who did not pass the previous training examination.
2.3 Payment Process
The training fee is RM 4,000.00 per person. Upon submission of the Registration Form, payment advice will be issued within 7 to 10 working days. Kindly make the payment to the provided account details to confirm your participation.
3. The training aims to equip and enhance new personnel with the essential knowledge, skills, and competencies of statutory requirements, regulatory updates, and industry best practices pertinent to medical device conformity assessments. It provides an opportunity to engage in practical exercises, case studies, and discussions, ensuring that you are well-equipped to excel in your role.
4. Your commitment to professional development is crucial, and we believe this training will contribute significantly in acquiring knowledge of the procedures and methodologies involved in conducting conformity assessments for medical devices. We look forward to your active participation in this valuable training session. Should you have any inquiries, please feel free to contact us using the details provided in the appended signature below.
Best regards,