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College aantekeningen

Pharmacy Law

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All Pharmacy laws within the UK. From how to check if a prescription is legally valid to the rules and regulations for wholesalers of pharmaceutical drugs

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Voorbeeld van de inhoud

The Pharmacist


UK Legislative System
 2 types of law:
o Criminal: Relationship between an individual and the state and relates to the
regulation of human behaviour
o Civil: relationship between individuals and relates to the conduct of human
relationships
Criminal Law
 Penal law
 Bodies of law with the potential for severe impositions as punishment for failure to
comply
 Criminal cases involve an action that is considered to be harmful to society as a
whole
Civil Law
 Dealing with disputes between individuals and/or organisations, in which
compensation may be awarded to the victim
 Civil cases usually involve privates disputes between persons or organisations
 Protect and enforce right of individuals
Criminal Law Vs. Civil Law
 Dispensing error: Criminal
 Pharmacists now need professional indemnity insurance. Requirement by pharmacy
regulator (GPhC)
Primary legislation
 Act of Parliament- Acts lay down general principle
 E.g. Medicines Act 1968
Formal procedure of enactment involves
 “White paper”- Government signals its intentions (before bill)
 Sometimes preceded by a “Green paper”- discussion document
 Cetin out proposals and inviting comments from invited parties
 Bill:
o Proposal to introduce new legislation
o Government bills (most)
o Private members bill= Individual MP bringing a bill to parliament
 Bill is debated in both houses of Parliament
 Passed
 Formal enactment takes place when he bill receives “Royal Assent” (Queen signs).
At this stage, the Bill is known as an Act
 Once passed, an Act cannot be altered or mended except by a further Act

,The Pharmacist




Secondary Legislation
 Most Acts delegate power to other bodies to make detailed rules= They are
“enabling”
 Subsidiary to an Act
 Normally in the form of Statutory Instruments
o Including regulations and orders

Statutory Instruments (SI)
 SI are concerned with wording detail
 SI is not complete in itself but refers back to the Act
 SI can amend a previous SI
 Initiated by a government minister under powers conferred by an Act
 Becomes law after “laying on the table” for 3 days
 Both Act and SI may have Schedules (like an appendix) which lists details better
separated from the main requirements
 Both Act and SI form Statutory Law
Judicial Precedent
 Known as case law, common-law or Judge-made law
 JP is a statement of the legal position in a particular case or situation based on the
decisions of previous courts in similar cases
 Judges make laws:
o If there is no law on a particular issue
o Where there is legislation, but its meaning is unclear

EU Law
 European Commission- Initiates most European Law
 Council of the EU- Makes ultimate decisions on European Law
 European Parliament- Directly elected chamber
 European Court of Justice- Decisions by them must be accepted by courts in member
states and there is no right of appeal
 Primary legislation is in the Treaties, which established the original communities
 Secondary legislation is:
o Regulations
 Direct effect and binding on all member states and individuals
o Directives
 Binding by their objectives but leave to member states method of
implementation (legislative or administrative)
 Are usually incorporated into UK law by use of SI
o Decisions

,The Pharmacist


 Binding to those to whom they are addressed to and often of an
administrative nature
 Harmonisation of laws by member states is usually by directives
Key Definitions
 Medicinal product:
o Having properties of preventing or treating disease
o Used or administered with a view to:
 Restoring, correcting or modifying a physiological function by exerting
a pharmacological, immunological or metabolic action
 Making a medical diagnosis
 Authorised medicinal product
o Authorised if there is in force for the product:
 Marketing authorisation
 Certificate of Registration
 Traditional herbal registration
 Article 126a authorisation
 Relevant medicinal product
o A medicinal product that is not:
 A registrable homeopathic medicinal product
 A traditional herbal medicinal product
 Medicinal purpose
o Treating or preventing disease
o Diagnosing disease or measuring the existence, degree or extent of physical
condition
o Contraception
o Inducing anaesthesia
o Otherwise preventing or interfering with the normal operation of a
physiological function, whether permanently or temporarily, and whether by
way of terminating, reducing, postponing, increasing or accelerating the
operation of that function
 Administer
o Orally, injection, or by introducing to the body in any other way
o By external application (whether or not by direct application to the body)

, The Pharmacist


Misuse of Drugs Act 1971
 Controls export, import, production, supply and possession of dangerous or other
harmful drugs
 Termed Controlled Drugs (CDs)
 Controls treatment of addicts
 General effect is to make unlawful all activities with drugs controlled by the Act
Schedule 2
 Morphine, diamorphine, methadone, fentanyl, alfentanil, oxycodone,
methylphenidate, dexamphetamine, ketamine
 3 classes based on degree of harmfulness, class are solely for the purpose of
determining penalties for offences:
o Class A
o Class B
o Class C

Legal Highs (NPs)
 Ban on novel psychoactive substances
o Psychoactive Substances Act, May 2016
 Made an offence to manufacture, import, supply, or distribute- but not possess:
o Any substance deemed to be psychoactive
o Exception of alcohol, tobacco, certain foods or medicines

Directions following convictions of practitioners for offences concerning CDs
 Pharmacists
o Prohibited from any possession, supply, dispensing, compounding etc of any
CD
 Retail pharmacy owner (or corporate body)
o Removal of premises from the register of pharmacies
 Similar effects for doctors
Misuse of Drugs Regulations 2001
 Permits use of CDs used as medicines
 Other regulations deal with:
o Misuse of Drugs (safe custody) Regulations 1973 Storage and safe custody
of CDs
o Health Act 2006”Accountable officer” Standard Operating Procedures
(SOPs)
 5 Schedules of CDs:
o Schedule 1 – CD Lic POM
o Schedule 2 – CD POM
o Schedule 3 – CD No Register POM
o Schedule 4

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Geüpload op
15 augustus 2021
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103
Geschreven in
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