689 Southbridge St, Auburn, MA 01501Call us at (508) 832-6511Open Mon–Fri: 8:30 a.m. – 7:00 p.m. · Sat: 9:30 a.m. – 4:30 p.m. · Sun: Closed689 Southbridge St, Auburn, MA 01501Call us at (508) 832-6511Open Mon–Fri: 8:30 a.m. – 7:00 p.m. · Sat: 9:30 a.m. – 4:30 p.m. · Sun: Closed
All Long-Term Care services

Long-Term Care Service

Regulatory Compliance

DPH, DEA, MA Board of Pharmacy, CMS — handled. Your facility doesn't need to keep them straight.

DPH, DEA, and state board requirements built into our workflow — survey-ready documentation included.

Regulatory Compliance

What this looks like in practice

Long-term care pharmacy operates at the intersection of multiple regulatory bodies, each with its own requirements: the Massachusetts Department of Public Health (facility licensure, controlled-substance handling), the DEA (CII–CV scheduling, destruction, and reconciliation), the Massachusetts Board of Pharmacy (pharmacy practice and dispensing), CMS (federal SNF requirements), and your individual facility's accreditor (TJC, CARF, etc.).

We've built our entire workflow around these requirements so you don't have to manage them separately. Controlled substance destruction follows DEA Form 41 protocols. Expired medications are returned with documentation. USP 800 hazardous drug procedures are followed for chemotherapy and other listed drugs. Recalls are caught by our system and communicated to your DON within 24 hours.

When surveyors arrive at your facility, they often want to talk to us too — and they get clean documentation, on time, every time. Our LTC partners consistently survey better on medication-management metrics than industry average.

What's included

  • DPH, DEA, MA Board of Pharmacy
  • Controlled substance destruction
  • USP 800 hazardous drug procedures
  • Recall and adverse-event coordination

24h

Recall communication SLA

Zero

Survey deficiencies attributable to us in 5+ years

Quarterly

Compliance audit cadence

What You Get

The benefits in detail.

Controlled Substance Compliance

CII–CV reconciliation, destruction (DEA Form 41), and reverse-distribution all handled by our pharmacy.

USP 800 Hazardous Drugs

Hazardous medication handling, packaging, and disposal follows USP 800 — surveyors increasingly look at this.

Recall Response

Our system flags recalled medications across all resident profiles. We communicate to your DON within 24 hours.

Survey Support

Our consultant pharmacist makes herself available during surveys to answer pharmacy-related questions on your behalf.

Who It's For

This is especially helpful for…

  • Skilled nursing facilities (CMS / state-regulated)
  • Group homes (DDS / DMH oversight)
  • Facilities preparing for survey
  • Operators upgrading existing pharmacy partnerships

How It Works

Three simple steps.

01

Compliance baseline

Initial audit of your current state vs DPH/DEA/CMS requirements. We document gaps and create a remediation plan.

02

Workflow integration

Our compliance procedures integrate into your med-pass routine. Quarterly audits keep things current.

03

Survey + ongoing oversight

Available during surveys, responsive to deficiencies, and proactive on regulatory changes.

Common Questions

Frequently asked questions.

Who handles the destruction of expired and unused medications?

We do. Quarterly pickup of expired medications, reverse distribution where applicable, and destruction with full DEA Form 41 documentation for controlled substances.

What if there's a survey deficiency related to medication?

We help you write the plan of correction and provide any pharmacy documentation surveyors request. We aim for zero medication-related deficiencies, but if one happens, we own it.

How do you handle USP 800?

Hazardous drugs are packaged separately with proper labeling, handled with required PPE, and disposed of per USP 800 standards. Most facilities don't need to think about it.

Are recalls always communicated?

Yes — our system cross-references active recalls against every resident's medication profile. Affected residents and your DON are notified within 24 hours of FDA recall posting.