MODULE 5 Flashcards
are the health professionals MOST ACCESSIBLE TO THE PUBLIC.
COMMUNITY PHARMACISTS
They supply medicines in accordance with a presciption or, when legally permitted, sell them without a prescription.
COMMUNITY PHARMACISTS
COUNSELING OF PATIENTS AT THE TIME OF DISPENSING of prescription and non-prescription drugs
COMMUNITY
DRUG INFORMATION to health professionals, patients and the general public
COMM PHARM
Participation in HEALTH-PROMOTION PROGRAMS
COMM PHARM
EXTEMPORANEOUS PREPARATION and small-scale manufacture of medicines
COMM PHARM
Responding to symptoms of minor ailments
COMM PHARM
Hospitals and other institutions and facilities, such as outpatient clinics, drug-dependency treatment facilities and long-term care facilities, maybe operated by the government or privately.
HOSPITAL PHARMACY
Has MORE OPPROTUNITY TO INTERACT CLOSELY WITH THE PRESCRIBER and promote the rational prescribing and use of drugs
HOSP PHARM
Having ACCESS TO MEDICAL RECORDS for assisting in the SELECTION OF DRUGS AND DOSAGE REGIMENS thus recommend changes where necessary;
HOSP PHARM
To MONITOR PATIENT COMPLIANCE and therapeutic response to drugs
HOSP PHARM
Recognize and report adverse drug reactions
HOSP PHARM
Serves as a member of POLICY-MAKING COMMITTEES like Pharmacy and Therapeutics Committee (P & TC), those concerned with drug selection, the use of antibiotics, and hospital infections and influences in the preparation and composition of an essential drug list or formulary
HOSP PHARM
Can control hospital manufacture and procurement of drugs to ensure the supply of high-quality products
HOSP PHARM
Takes part in the PLANNING AND IMPEMENTATION OF CLINICAL TRIALS.
HOSP PHARM
provide PATIENT CARE that optimizes MEDICATION THERAPY and promotes health, disease prevention and promotes RATIONAL MEDICATION USE
CLINICAL PHARMACY
works DIRECTLY with medical professionals and patients, usually in a medical center, hospital or health care unit.
CLINICAL
determine the BEST MEDICATIONS for a given symptom for a patient at a given time.
CLINICAL
are responsible in monitoring PATIENT’S RESPONSE to drug therapy
CLINICAL
are responsible for selecting APPROPRIATE DRUGS, for monitoring the progress of their patients, for diagnosing potentially untreated illnesses, for consulting with the patient on the effects of the drugs, and for ensuring the patients follow prescribed drug regimens.
CLINICAL
work mainly on (1) contributing to the DEVELOPMENT OF MEDICINES and (2) EVALUATING PHARMACEUTICAL CARE and services.
DRUG RESEARCH
ASSIST INVESTIGATORS in basic, clinical and translational research
DRUG RES
work with other SCIENTISTS to DEVELOP AND SELECT DRUG COMPOUNDS that maybe valuable as medicines during the discovery phase
DRUG RESEARCH
Design a research plan, apply research protocol and disseminate the results of the research
DRUG RES
a field that specialized in CREATING DRUGS AND MEDICATIONS.
MANUFACTURING / INDUSTRIAL PHARMACY AND QUALITY ASSURANCE
Research drug compounds and develop new medications based on research
MANU / INDUS PHARM & QUALITY ASSURANCE
TEST medications for efficiency and safety
MANU / INDUS PHARM & QUALITY ASSURANCE
OVERSEE THE PRODUCTON PROCESS to ensure medications are produced accurately
MANU / INDUS PHARM & QUALITY ASSURANCE
Engage MARKETING AND PROMOTING NEW DRUGS to consumers, hospitals and doctor’s offices
MANU / INDUS PHARM & QUALITY ASSURANCE
Conducting CLINICAL DRUG TRIALS AND EVALUATING THE RESULTS of these trials to gauge a drug’s effectiveness and to determine potential risks or side effect
MANU / INDUS PHARM & QUALITY ASSURANCE
ensures an INTEGRATED APPROACH to quality assurance (including good manufacturing practice) through the validation of the various stages of production and the testing of products before release.
QA ANALYST
BATCH RELEASE of manufactured “specials” including solutions, suspensions, powders, capsules, creams and ointments and other non-sterile dosage forms
M/I PHARM & QA
REVIEWING AND APPROVING OF QUALITY DOCUMENTATION including validation protocols and reports, change controls and Good Manufacturing Practices deviations
M/I PHARM & QA
Writing and approving of Standard Operating Procedures
M/I PHARM & QA
Involvement with technical customer queries and product investigations
M/I PHARM & QA
Responding to enquiries in a timely manner, giving advice on “specials” quality requirements in order to maintain the Company’s reputation for customer service and technical insight
M/I PHARM & QA
Participating in self-inspections and regulatory inspections
M/I PHARM & QA
engage in EDUCATION, pharmaceutical practice and research in schools of pharmacy. Undergraduate, postgraduate and continuing education require the educators to have expertise in the various pharmaceutical sciences.
PHARMACIST IN THE ACADEME
Duties include administrative activities, scientific research, teaching professional student pharmacists
ACADEME
Supervising research and teaching graduate students
ACADEME
Speaking and/or publishing in scientific venues
ACADEME
Teaching student pharmacists through experiential practice
ACADEME
sometimes called as MEDICO-MARKETING or PHARMA MARKETING
PHARMACEUTICAL MARKETING AND RETAIL
PHARMACEUTICAL MARKETING AND RETAIL is sometimes called as
MEDICO-MARKETING / PHARMA MARKETING
engaged in ADVERTISING AND PROMOTING THE SALE of pharmaceutical drugs.
PHARMACEUTICAL MARKETING & RETAIL
involves MANAGEMENT OF MARKETING PROGRAMS that promote products to health-care professionals, while assisting with sales goals.
MARKETING & RETAIL
Management of MERCHANTS and EXTERNAL MARKETING AGENCIES engaged in company promotions
MARKETING & RETAIL
Branding, communications and development are also common responsibilities
MARKETING & RETAIL
Development of business strategies, such as pricing strategies
MARKETING & RETAIL
Identify and analyze competitions
MARKETING & RETAIL
Research new target markets
MARKTING & RETAIL
Assists with events and trade-show activities
MARKETING & RETAIL
They are known as “Regulatory Pharmacist”
PRODUCT REGULATION
involved in ALL STAGES OF DEVELOPMENT and marketing of drugs
PRODUCT REGULATION
Obtaining AUTHORIZATION of medicines for use in clinical trials
PRODUCT REGULATION
Registration and marketing and the POST-APPROVAL SURVEILLANCE ACTIVITIES such as safety updates, licensing applications for prescribing information, new clinical uses or new formulations, etc.
PRODUCT REGULATION
ACT AS THE LINK between the company and the local regulatory authorities on matters relating to the quality, safety and efficacy issues of drugs.
PRODUCT REGULATION
is defined as the science and activities relating to the detection, assessment, understanding and PREVENTION OF ADVERSE EFFECTS or any other drug-related problem.
PHARMACOVIGILANCE
Collect and record information during drug PRECLINICAL DEVELOPMENT and clinical trials
PV
Collect and record adverse drug reactions
PV
Creates STANDARD OPERATING PROCEDURES, individual case study report, literature screening and regulatory reporting
PV
involved in ADVACNE PHARMACY PRACTICE, health policy development, emergency and humanitarian response and global health. This is primarily concerned with health education, health promotion and disease prevention interventions.
PUBLIC HEALTH AND PHARMACEUTICAL POLICY
Provide public health services
PUB HEALTH
Act as INFORMATION RESOURCES on lifestyle changes that can influence healthy outcomes.
PUB HEALTH
Involved in HEALTH SCREENINGS (e.g. diabetes, cholesterol, osteoporosis), immunizations, pain control, participatory and counseling/health education.
PUB HEALTH
Provide INFORMATION ON SELF-MANAGEMENT (hypertension, asthma, HIV), smoking cessation, alcohol, tobacco and other drug use prevention, family planning, medication indications and conditions (like dyslipidemia).
PUB HEALTH
