Application For Licenses At Prescribed Forms ( 86 )

The task of completing the Controlled Drugs Register can be delegated by the prescribing officer to another member of staff, however, responsibility for the supply remains with the prescribing officer.

A prescription can be identified as legally authorised written instruction by a prescribing officer to a pharmacist to dispense medication.

However, he is in graduate school perusing an M.B.A. There is constraint as to which retailers will be able to carry the product since the retailer will have to be licensed to sell alcohol in their establishment.

Prescription of medicines (POM). These are only available from a pharmacist if they are prescribed by an appropriate doctor.

1. The current legislation, guideline policies and protocols relevant to the administration of medication are.

There are several types of medication, each has a purpose and function needed for their administration via the different routes.

The person dispensing must also be appropriately trained, follow safe systems of work and understand the side effects of various drugs; be able to access appropriate information and understand when to access advice or further information

Non care setting - Medications are often stored and administered in a variety of non-health care settings. These settings include: primary and secondary schools, Child day care centres, Board and care homes, Jails and prisons. In all these settings, employees frequently are responsible for handling and administering prescription and over-the-counter medications to clients or residents. Some organizations may employ licensed health professionals to directly manage the medication administration process. However, many of these settings have no licensed health professionals involved. Where medications are stored and administered to individuals, written policies and procedures should address the following: Acquisition of medications (e.g., from parents, caregivers, pharmacies), Specification of which personnel are allowed access to medications and allowed to administer medications to students, clients or residents, Labelling and packaging of medications managed for students, clients

* Trained and designated care workers give controlled drugs, another trained, and designated staff should witness. (Standard 9.7 and 20.9)

The principle reason for the Act is to keep the abuse of controlled medications and attains to this by forcing a complete boycott on the ownership, supply, make, import and fare of controlled medications with the exception of as permitted by regulations or by permit from the Secretary o

There are several legislations in place with protocols for the administration of medication which I have listed below. The main policy re admin of drugs and storing of drugs and medicines is the Control Of Substances Hazardous to Health or COSHH but along with this there are other policies in place as per the list below.

Right Drug: Check that these are the medicines that are on the person’s Medicine Administration Record (MAR).

Legislation – The Medicines Act, Control of Substances Hazardous to Health (COSHH) Regulations, The Health and Safety at Work Act, The Misuse of Drugs Act, The Misuse of Drugs (Safe Custody) Regulations, Health and Social Care Act

Statewide regulation of pharmacists in Texas began in 1907 with the passage of the Texas Pharmacy Act, creating the Texas State Board of Pharmacy. The purpose of the act is to promote, preserve and protect public health, safety and welfare through effective control and regulation of the practice of pharmacists and licensing of pharmacies engaged in the sale, delivery or distribution of prescription drugs and devices (Senate Bill 82, 30th Legislature, Regular Session). Before the Pharmacy Act was enacted, pharmacists were regulated locally by district boards, each composed of three pharmaceutical examiners, beginning in 1889 (House Bill 125, 21st Legislature, Regular Session).

Such persons or individuals must register with the Drug Enforcement Authority (DEA) whom provides the authorisation and regulation for the access (Food and Drug Administration 2009). Yeh 2012 wrote that registration is granted on a “public interest” basis, generally relating to public health, safety and compliance with state law.