Human Medicines Regulations (HMR) Schedule 17 Exemptions Training (NW241120A)

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Registration from 12.45

*There will be a requirement to complete a portfolio of 5 cases before a "Certificate of Completion" will awarded and must be completed within 3 months of training.

You will be sent a Microsoft Teams invitation no later than Monday 18th November 2024 please check your spam/junk emails.

It is advised that where possible, you use a laptop/PC.

Late Bookings Policy:

Any bookings made within 24 hours of the course commencement date are considered late bookings. It is crucial for us to maintain the quality of our courses and ensure a seamless experience for all participants. Therefore, late bookings may not receive an automatic link to the course.

Action Required:

If you have booked on a course within 24 hours of its start time, we kindly request that you contact the course organiser immediately elaine.douglas@nhs.net. Failure to do so may result in:

1. No Access to the course: You may not receive the link to join the webinar automatically or have reserved a place at a venue.

2. Potential Charges: Depending on the circumstances, there may be charges associated with late bookings

Mandatory: Dental Hygienist, or Dental Therapist

To equip dental hygienists and dental therapists with the knowledge and skills necessary to safely and effectively administer and supply specific medicines within the legal framework of Human Medicines Regulations.

Knowledge of legislation

Demonstrate an understanding of the legal framework of the Human Medicines regulations and its relevance to the practice of dental hygiene and dental therapy.

Identify the legal and professional boundaries regarding administration and supply of specific medicines within dental clinical practice

Clinical practice

Conduct comprehensive patient assessment to determine the need for specific medicines, considering patient history current medications and potential allergies.

Informed consent

Effectively communicate with patients to obtain informed consent ensuring patients understand the purpose, benefits and any risks involved in the administration and supply of medicines provided.

Monitoring and management

Monitor patients for adverse reactions and manage any complications effectively including providing the appropriate documentation and aftercare.

Reporting adverse events

Identify, document and report adverse drug reactions promptly and appropriately following established protocols

Reflective practice

Use reflective practice to evaluate personal performance and identify areas of improvement in the safe administration and supply of specific medicines

To enable delegates to safely and effectively administer and supply specific medicines within the legal framework of Human Medicines Regulations, ensuring the highest standards of patient care and adherence to professional and ethical guidelines