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Third-party lab reports publishedSee our test resultsFree EU shipping over 300 €Tracked delivery across the EUResearch use onlyThird-party lab reports publishedSee our test resultsFree EU shipping over 300 €Tracked delivery across the EUResearch use only
Third-party lab reports publishedSee our test resultsFree EU shipping over 300 €Tracked delivery across the EUResearch use onlyThird-party lab reports publishedSee our test resultsFree EU shipping over 300 €Tracked delivery across the EUResearch use only

Regulatory & Industry

Home/Archive by Category "Regulatory & Industry"
A shallow glass dish of blue-green solution on a formulation bench, the topical form in which the GHK-Cu human trials were done.
author-avatar Peptra Labs Research
Regulatory & Industry
09 Sep 2026
September 9, 2026

GHK-Cu: 50 Years of Research, None on Injection

GHK-Cu has decades of human trials as a topical serum and none as an injection, NPR reports, with an FDA panel reviewing the injectable in February.
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An opened polystyrene shipper with fully thawed gel packs on a goods-in bench, the transit question MSK raises about wellness peptides.
author-avatar Peptra Labs Research
Regulatory & Industry
08 Sep 2026
September 8, 2026

Peptides and Cancer: What Memorial Sloan Kettering Says

Peptides sold online for wellness have not been through clinical trials, and Memorial Sloan Kettering has now told patients why that matters.
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An empty committee room with a long table and identical chairs, the setting where GLP-1 guidelines get written.
author-avatar Peptra Labs Research
Regulatory & Industry
05 Sep 2026
September 5, 2026

GLP-1: WHO Guidelines, 1 Billion People, 3 Industries

GLP-1 now has a WHO guideline, and a Science editorial names the three industries competing around it: pharmaceutical, food and wellness.
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Two identical unlabelled cartons in cold storage, of the kind holding the blinded supply for a tirzepatide comparison trial.
author-avatar Peptra Labs Research
Regulatory & Industry
29 Aug 2026
August 29, 2026

Tirzepatide CV Approval: The Overlooked 0.92 Hazard Ratio

Tirzepatide gained an FDA cardiovascular indication on 28 August 2026, from a trial that met non-inferiority and missed superiority at P = 0.09.
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