Final answer:
Notification requirements for performing DTM can vary depending on country and regulations, while CE requirements depend on the professional and field of genetics.
Step-by-step explanation:
Notification requirements for performing Direct-to-Consumer Genetic Testing (DTM) vary depending on the country and specific regulations. In the United States, for example, laboratories that offer DTM services need to comply with the Clinical Laboratory Improvement Amendments (CLIA) regulations and may require FDA approval for certain tests. Additionally, some countries have regulations that require notification to healthcare professionals or genetic counselors when offering DTM services.
Continuing Education (CE) requirements for performing DTM depend on the professional involved and the specific field of genetics. For example, clinical geneticists, genetic counselors, and laboratory directors may be required to complete a certain number of continuing education credits in genetics or related fields to maintain their certifications and licenses.