GA MPJE study plan

Map each licensure pathway in Domain 1 (pharmacist, technician, pharmacy, and nonresident/outsourcing registration) against its statutory authority and cite the governing provision for each

Differentiate pharmacist scope-of-practice activities from those requiring additional authorization, and write a one-line rule for each activity

Build a comparison chart of CSA schedules I-V listing criteria, examples, and federal registration requirements

Explain the federal prescription requirements for Schedule II versus Schedule III-V drugs, including refill and transfer rules

Compare Georgia controlled substance provisions against the federal CSA and list every point of divergence with the stricter rule flagged

Sequence the required elements of a valid prescription (prescriber identifiers, drug, directions, quantity, refills, signature) and identify which omissions make a prescription invalid

Apply the rules for Schedule II partial fills, emergency oral prescriptions, and dispensing without a prescription where permitted

Draft the labeling content required at dispensing for both legend and controlled substances

Organize Board of Pharmacy rule topics (facility standards, equipment, security, personnel) into a checklist format

Distinguish what the Practice Act statute requires from what the Board rules add, for at least 10 overlapping requirements

Practice resolving scenario questions on prescription transfers, refills, and substitution by writing the controlling rule before selecting an answer

Identify the recordkeeping obligations triggered by each dispensing event (prescription retention, controlled substance records, counseling documentation)

Map the licensure lifecycle (initial application, renewal cycle, continuing education, reinstatement) for pharmacists and technicians

Categorize grounds for discipline and the Board's disciplinary process steps in order

Build an inventory-tracking reference for controlled substances, covering biennial inventory, receipt records, and disposal/return documentation

Reconcile a sample perpetual inventory problem and identify where a discrepancy would be reportable

Sequence the recordkeeping retention periods for prescriptions, controlled substance records, and inventory documents, and flag any that differ

Explain the legal pathways for drug distribution (manufacturer, wholesaler, repackager) and the registration or licensure each requires

Differentiate prescription drug marketing restrictions from permissible promotional activity

Identify the requirements for handling recalls, returns, and suspect or illegitimate product

Apply patient counseling requirements to specific dispensing scenarios, including when counseling may be declined or delegated

Explain privacy obligations for protected health information in the pharmacy workflow, including minimum-necessary and disclosure scenarios

Evaluate professional standard-of-care questions involving medication errors, DUR, and documentation

Resolve mixed-domain scenarios that combine counseling with controlled substance dispensing requirements

Complete a full-length timed simulated exam under test conditions

Review every missed item and classify the error as knowledge gap, misread, or rule confusion

Re-drill the two lowest-scoring domains with targeted original questions

Rewrite weak rules into one-sentence memory cues

Re-take a condensed high-yield set weighted to the three heaviest domains and confirm improvement over week 7

Recite from memory the key numeric thresholds (retention periods, inventory cycles, renewal intervals, refill limits)

Walk through two full prescription-to-dispensing scenarios end to end without notes

Finalize a one-page pre-exam reference sheet limited to items you have repeatedly missed