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We will visit your facility on a monthly or quarterly basis to conduct medication regimen and peer reviews, regulatory audits, leadership team, and provide in-service training. We will also inspect medication storage, handling and disposal, audit controlled substances and much more. We will exceed your expectations!
PharmD USA’s on-site clinical pharmacists visit your outpatient mental-health clinic on a set schedule to perform comprehensive chart and peer reviews. We verify psychotropic regimens, flag drug–drug interactions, reconcile lab values, and benchmark individual prescribers’ patterns against best-practice guidelines—promoting safer, more consistent care across the team.
During each visit we inspect medication rooms, refrigerators, sample cabinets, and controlled-substance logs, auditing crash carts and expiration tracking systems to keep inventory secure, organized, and survey-ready. Findings feed directly into the clinic’s continuous-quality-improvement (CQI) plan, generating actionable tasks and follow-up timelines.
We facilitate Medication Management / Pharmacy & Therapeutics meetings, supplying data dashboards that track metabolic-monitoring rates, antipsychotic polypharmacy trends, benzodiazepine taper progress, and antibiotic-use indicators. These metrics drive CQI projects that are revisited at every on-site session, ensuring steady progress and clear documentation of outcomes.
All activities are mapped to state, DEA, and accreditation standards, with detailed compliance checklists and gap analyses delivered after each visit. This proactive approach positions your clinic to excel in regulatory and accrediting-body surveys while continuously elevating patient safety and therapeutic effectiveness.
Let us create or improve your current policies to ensure they exceed expectations set by local and federal government surveyors. Our policies revolve around regulations set by such agencies as CMS, Joint Commission, DEA, Departments of Health, and Boards of Pharmacy. We will help your facility create or improve existing Standing Drug Orders, policies, forms, automatic therapeutic substitutions, and formulary establishment.
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