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Recognition
Inclusion & Diversity
More info
Workforce Wellbeing
More info
Pharmacist Prescribing
More info
RPS in Scotland
RPS in Wales
RPS in England
Ambassadors
Podcasts
Policies
Knowledge
e-Library
MEP
The PJ
Pharmacy Guides
Other publications
Pharmacy Alerts
Research Journals
Development
Students
More info
Trainee Pharmacists
More info
Pharmacists and Pharmaceutical Scientists
More info
Revalidation
Education & Training
Consultants
Career Support
Mentoring
Events
Webinars
e-Portfolio
Your Membership
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Chapters
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Foreword
1. Changes To MEP
2. Core Concepts and skills
Back
2.1 Professional Conduct
Back
2.1.1 Professionalism
2.1.2 Professional judgement
2.1.3 Professional empowerment
2.1.4 Standards and guidance
2.1.5 Conflicts of interest
2.1.6 Interface between personal and professional lives
2.1.7 Professional indemnity
2.2 Professional Development
Back
2.2.1 Revalidation
2.2.2 Development frameworks and recognition
2.2.3 Pharmacist prescribing
2.2.4 Mentoring
2.3 Research
Back
2.3.1 Pharmacists in research
2.3.2 Research ethics
2.4 Patient or Person-Centred Healthcare
Back
2.4.1 Person-centred healthcare
2.4.2 Being culturally informed
2.5 Patient Safety
Back
2.5.1 Getting the culture right
2.5.2 Culture and patient safety incidents
2.5.3 Reporting adverse events
2.5.4 Risk Management
2.5.5 Handling dispensing errors
2.5.6 Safeguarding
2.5.7 Clinical Audit
2.6 Pharmaceutical Care
Back
2.6.1 Development of pharmaceutical Care
2.6.2 Principles of pharmaceutical care
2.6.3 Medicines optimisation
2.6.4 Medicines reconciliation
2.6.5 Clinical check
2.6.6 Medication review
2.6.7 Patient consultations
2.7 Sustainability
3. Underpinning Knowledge - Legislation and Professional Issues
Back
3.1 Classification of medicines
Back
3.1.1 General sale medicines
3.1.2 Pharmacy (P) medicines
3.1.3 Prescription-only medicines (POM)
3.1.4 Reclassified medicines
3.2 Professional and legal issues: pharmacy medicines
Back
3.2.1 Pseudoephedrine and ephedrine
3.2.2 Oral emergency contraception
3.2.3 Paracetamol and aspirin
3.2.4 Codeine and dihydrocodeine
3.3 Professional and legal issues: prescription-only medicines
Back
3.3.1 General prescription requirements
3.3.2 Dental prescriptions
3.3.3 Faxed/digital copies of prescriptions
3.3.4 Forged prescriptions
3.3.5 Prescriptions from the EEA or Switzerland
3.3.6 Military prescriptions
3.3.7 Labelling of dispensed medicinal products
3.3.8 Administration
3.3.9 Patient specific directions and administration, sale or supply in hospitals and other settings
3.3.10 Exemptions: sale and supply without a prescription
3.3.11 Pregnancy prevention programmes
3.3.12 Biosimilar medicines
3.3.13 Advanced therapy medicinal products (ATMPs)
3.3.14 Prescriber types and prescribing restrictions
3.3.15 Checking registration of healthcare professionals
3.3.16 Prescribing and dispensing by the same person
3.3.17 Dispensing self-prescribed prescriptions and prescriptions for close friends and family
3.3.18 Self-Checking Prescriptions
3.4 Wholesaling
Back
3.4.1 Wholesaler licence requirements
3.4.2 Wholesaling of controlled drugs
3.4.3 Persons and organisations that can receive medicines
3.4.4 Signed orders and record keeping
3.4.5 Wholesaling and medicine shortages
3.5 Veterinary Medicines
Back
3.5.1 Prescription requirements for POM-V, POM-VPS and medicines supplied under the veterinary Cascade
3.5.2 The veterinary Cascade
3.5.3 Labelling of dispensed veterinary medicines
3.5.4 Record keeping
3.5.5 Wholesaling veterinary medicines and temporary supply shortages
3.5.6 Selling veterinary medicines on the internet
3.6 Controlled Drugs
Back
3.6.1 Background
3.6.2 Classification
3.6.3 Possession and supply
3.6.4 Administration of Controlled Drugs
3.6.5 Import, export and travellers
3.6.6 Obtaining Controlled Drugs – requisition requirements for Schedule 1, 2 and 3 Controlled Drugs
3.6.7 Prescription requirements for Schedule 2 and 3 Controlled Drugs
3.6.8 Collection of dispensed Controlled Drugs
3.6.9 Safe custody
3.6.10 Destruction of Controlled Drugs
3.6.11 Record keeping and Controlled Drugs registers
3.6.12 Extemporaneous methadone
3.6.13 Cannabis and cannabis-based products
3.7 Additional legal and professional issues
Back
3.7.1 Expiry dates
3.7.2 Waste medicines
3.7.3 Requests for poisons and chemicals
3.7.4 Delivery and posting of medicines to patients
3.7.5 Secure environments
3.7.6 Child-Resistant Packaging
3.7.7 Homeopathic and herbal remedies
3.7.8 Charitable donation of medicines
3.7.9 Collection and purchase of medicines by children
3.7.10 Medical devices
3.7.11 Multi-compartment compliance aids
3.7.12 Drugs and driving
3.7.13 Retention of pharmacy records
3.7.14 New Psychoactive substances
3.7.15 Working during a pandemic
3.7.16 Needle Syringe Provision
4. The Responsible Pharmacist
5. Royal Pharmaceutical Society Code of Conduct
6. Pharmacist Support
7. Appendices
Acknowledgements
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Appendices
Acknowledgements
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Medicines, Ethics and Practice
3. Underpinning Knowledge - Legislation and Professional Issues
3.6
Controlled Drugs
3.6.1 Background
3.6.2 Classification
3.6.3 Possession and supply
3.6.4 Administration of Controlled Drugs
3.6.5 Import, export and travellers
3.6.6 Obtaining Controlled Drugs – requisition requirements for Schedule 1, 2 and 3 Controlled Drugs
3.6.7 Prescription requirements for Schedule 2 and 3 Controlled Drugs
3.6.8 Collection of dispensed Controlled Drugs
3.6.9 Safe custody
3.6.10 Destruction of Controlled Drugs
3.6.11 Record keeping and Controlled Drugs registers
3.6.12 Extemporaneous methadone
3.6.13 Cannabis and cannabis-based products
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Purchase MEP 46 (July 2023)
Index terms:
Accountable, Accountable officer ,CD