Non-maleficence, or the principle of 'do no harm,' is the primary ethical principle that guides medical education and training in India. It emphasizes the importance of avoiding causing harm to patients or students during the process of medical education and training.

The National Medical Commission Act, 2019 is the primary legal framework that governs medical education and training in India. It replaced the Indian Medical Council Act, 1956 and established the National Medical Commission (NMC) as the apex regulatory body for medical education and training in the country.

The National Medical Commission (NMC) is responsible for regulating medical education and training institutions, approving medical colleges and courses, conducting medical entrance exams, and granting licenses to medical practitioners in India.

All of the above statements are true. Patients must provide informed consent before participating in medical education and training activities, consent must be obtained from the patient's legal guardian if the patient is a minor or lacks the capacity to consent, and patients have the right to withdraw their consent at any time.

Medical negligence in medical education and training can result in civil liability for damages, criminal liability for gross negligence, and disciplinary action by the National Medical Commission.

All of the above statements are true. Animals should be used only when there are no other viable alternatives, animals should be treated with respect and compassion, and the number of animals used should be minimized.

All of the above statements are true. Medical waste must be segregated and disposed of in accordance with the Biomedical Waste Management Rules, 2016, medical waste must be incinerated or treated using other approved methods, and medical waste must be disposed of in a manner that prevents environmental pollution.

All of the above statements are true. Researchers must obtain informed consent from human subjects before conducting research, researchers must protect the privacy and confidentiality of human subjects, and researchers must minimize the risks to human subjects.

All of the above statements are true. Clinical trials must be approved by the Central Drugs Standard Control Organization (CDSCO), clinical trials must be conducted in accordance with the Good Clinical Practice (GCP) guidelines, and clinical trials must be registered with the Clinical Trials Registry - India (CTRI).

All of the above statements are true. Technology should be used to enhance the learning experience of students, technology should be used to improve the quality of patient care, and technology should be used to promote equity and access to medical education and training.