Peptides are everywhere. Safe access should be too.

Research-grade products moved quickly into the longevity market, often outside the traditional medical and pharmacy system. Now, the medical community and federal regulators are addressing the need for a safer, more responsible path to peptide care.

At the biostation, that physician-led model is already in place—and your evaluation can start today.

Educational information only. Treatment decisions require an individual medical evaluation.
Compounded medications are not FDA-approved.

How the Peptide market got here

Peptide interest moved fast.
The medical system had to catch up.

1

Interest Grew

Patients began seeking peptides for recovery, metabolic health, performance, and healthy aging.

2

Research-Grade Products Spread

Research-grade products became widely available without proper prescribing, sourcing, or clinical monitoring.

3

Longevity Experts Responded

Licensed providers and regulators held hearings, emphasizing appropriate evaluation, pharmacy standards, and patient safety.

The final hearing outcomes

What happened at the FDA peptide hearing?

On July 23 and 24, 2026, the FDA's Pharmacy Compounding Advisory Committee reviewed seven peptide-related bulk drug substances for potential inclusion on the Section 503A Bulk List.

Recommended for potential inclusion

BPC-157
TB-500
Epitalon
KPV
MOTS-C
Semax

Why this matters

Patients seeking these peptides are now required to be evaluated by licensed medical providers, prescribed, and sourced from a 503A FDA approved compounding pharmacy.

Access

Access

Patients deserve informed access through a legitimate care pathway.

Quality

Quality

503A-licensed compounding pharmacies follow defined regulatory standards.

Clinical Oversight

Clinical Oversight

Medical supervision helps guide dosing, follow-up, and monitoring.

Patient Safety

Patient Safety

Licensed pharmacy sterility testing, potency, and trust what you are introducing to your body.

the biostation approach

We have practiced patient-specific, physician-led peptide care for years.

Long before this hearing, our model centered on clinical evaluation, individual prescriptions, pharmacy coordination and ongoing care—not direct-to-consumer research products.

Licensed medical evaluation

Every patient begins with a provider review of health history, goals, medications and comprehensive bloodwork.

Individualized prescription

When prescribed, treatment is entered for an identified patient—not purchased as a general "research" product.

State-Licensed 503A pharmacy coordination

We coordinate prescriptions through licensed compounding pharmacies operating under applicable state and federal requirements.

Monitoring and follow-up

Progress, tolerability, labs when indicated, and care-plan changes are overseen by our medical team.

Your comprehensive wellness program includes:

Performance Blood Panel

In-depth Provider Consultation

InBody Composition Test

bID Personalized Plan

Dedicated Care Team

Ongoing Monitoring

After your consultation, you will receive a full recap and personalized plan of the recommendations that you discussed with your medical provider. This plan is referred to as your bID.

Schedule Your Peptide Consultation

In the news

FAQs

Questions patients are asking now.

Did the FDA approve BPC-157, KPV, TB-500, MOTS-C, Epitalon or Semax?

No. An FDA advisory committee recommended the six substances for potential inclusion on the 503A Bulks List. Advisory recommendations are non-binding and are not equivalent to FDA approval of a drug.

What is the Section 503A Bulks List?

It is a federal list of certain bulk drug substances that may be used in patient-specific compounding under specified conditions when an applicable USP or NF monograph does not exist and the substance is not a component of an FDA-approved drug product.

When could peptide availability change?

There is no guaranteed date. FDA must determine whether and how to act on the recommendations, which may involve notice-and-comment rulemaking or other policy action. Until then, patients should not assume the vote changed current access.

Are compounded peptide medications FDA-approved?

No. FDA states that compounded drugs are not FDA-approved and are not reviewed before marketing for safety, effectiveness or quality. That makes licensed clinical oversight, appropriate pharmacy sourcing and informed consent especially important.

Does the biostation subscription guarantee a peptide prescription?

No. Enrollment or interest does not guarantee treatment. A licensed provider must determine that a specific treatment is clinically appropriate, available and permitted under applicable law.

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