These are research-grade compounds verified by independent labs for purity, identity, and concentration. In other words, a separate company tests and verifies what is in each product.

A crucial document detailing its identity, quality, and purity, confirming it meets specifications for research or clinical use. These must be present upon request by any person or company that wishes to verify the products authenticity.

Current Good Manufacturing Practices certification isn't a single certificate but a regulatory standard enforced by agencies like the FDA to ensure products are consistently made, controlled, and safe, preventing contamination, errors, and mix-ups through strong quality systems. Companies undergo audits by accredited third parties or regulators to verify compliance, demonstrating commitment to quality, purity, and efficacy, which builds consumer trust and opens market access.

A facility that manufactures, repacks, or re-labels products (drugs, medical devices, food) has provided its contact and product information to the FDA. It is a mandatory administrative process, not an endorsement,, certification, or approval of product safety by the agency.

Direct to Consumer is a business model where manufacturers sell directly to the patient. Peptides, like prescription medications, should be prescribed under the direction of a medical provider such as an NP, PA or MD. Proper medical history intake and labwork should be done prior to starting Peptides.