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Methylcobalamin and Light: What Happens After the Vial Leaves the Carton
Methylcobalamin and Light: What Happens After the Vial Leaves the Carton

Your treatment room lights could be weakening your methylcobalamin before it ever reaches the patient, and the vial will still look perfectly normal. Learn why ordinary room light breaks down B12 and the three simple habits that make sure every patient gets the full dose you prescribed.

HHS Allows 503A Pharmacies to Compound Six Peptides, With Conditions. Here's What That Means
HHS Allows 503A Pharmacies to Compound Six Peptides, With Conditions. Here's What That Means

Six peptides, including BPC-157, can now be compounded by 503A pharmacies, but only if every strict condition is met. HHS's new policy is temporary, it isn't FDA approval, and it doesn't cover 503B outsourcing facilities. Here's what changed, what didn't, and six questions to ask any pharmacy before you order.

The White House Is Reviewing an FDA Peptide Policy. Here’s What That Means
The White House Is Reviewing an FDA Peptide Policy. Here’s What That Means

The Food and Drug Administration (FDA) has drafted a temporary policy that may allow pharmacies to compound certain peptides. It’s under White House review. Nobody outside government has seen it, and nothing has changed yet. Whether you’re a patient, a nurse or a physician, here’s what’s known and what isn’t.

FDA Advisory Committee Recommends Six Peptides for 503A Compounding
FDA Advisory Committee Recommends Six Peptides for 503A Compounding

On July 23–24, 2026, FDA's Pharmacy Compounding Advisory Committee recommended six peptides for the 503A bulks list: BPC-157, KPV, TB-500, MOTS-c, Epitalon and Semax. It voted against Emideltide (DSIP). The recommendation is advice to FDA, not a final decision, so these peptides still can't be legally compounded, and the vote doesn't apply to 503B outsourcing facilities. Here's what the vote means for your practice and what FDA has to do next.

Why we use pharmaceutical grade and FDA registered API for our drugs
Why we use pharmaceutical grade and FDA registered API for our drugs

The FDA recently reminded compounders about the risks of using dietary supplement-grade glutathione in injectable preparations. Learn how McGuff Outsourcing Solutions approaches API sourcing, bacterial endotoxin testing, and quality controls for Glutathione Injection.

Spring 2026 503B Update
Spring 2026 503B Update

Review our latest update from McGuff Outsourcing Solutions on our 503B outsourcing facility and product availability. We anticipate a June 2026 product launch and look forward to doing business with healthcare practitioners nationwide. 

Coronavirus (COVID-19)

Due to the Coronavirus (COVID-19) outbreak worldwide, the global demand for some Personal Protective Equipment (PPE) is exceeding current supply availability.

In addition, the manufacturing of the PPE and many other wound care/infection prevention products have been impacted by the global response to the Coronavirus. While you may see product availability reduction in the near-term, please be assured that we at McGuff Medical are continuing to work diligently to ensure an uninterrupted supply of products and alternative products to you.

Additionally, in order to ensure healthcare providers have access to the PPEs they need, the McGuff Company is temporarily limiting PPEs to healthcare providers.

As always, please feel free to reach out to our McGuff Customer Service team with any questions that you may have.

Click here for updates regarding Coronavirus Pandemic and Your Supplies and a message from our President