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CytoVive® Research Products
Peptides - SARMS - Nootropics

CytoVive® Medical Equipment & Testing Supplies 

The CytoVive® Standard

At CytoVive® we believe that all humans and animals deserve access to next generation treatments, and our mission is to bring healthcare professionals, veterinarians, and scientific researchers that next generation of functional medicine solutions.

All CytoVive® Medical Devices, Allograft Aliquots, and Research Chemicals go through an extensive vetting process for the following criteria: 

1. Devices must have no adverse events and only minimal (if any) side effects reported with use.   

2. Devices must possess proprietary qualities that revolutionize their respective application(s).   

3. Devices must be FDA registered and regulated -       

A) Under 21 CFR Part 1271 & PHS Act Section 361; or       

B) As a Class 2 510(k) approved device under 21 CFR Part 807.92 (a) (3).      

C) As a 505(b)(2) NDA Pharmaceutical under the Federal Food, Drug, and Cosmetic Act.       

D) Under Section IV.D of the FDA's Policy for Diagnostic Tests for Coronavirus Disease-2019.  

4. Allograft Tissue Aliquots - must be certified by an independent third party laboratory (registered as a 501(c)(3)) for product sterility and viability. 

*Products regulated by criterial 1-4 are available from CytoVive LLC at Research Chemicals are available from CytoVive Laboratories LLC at

5. Research Chemicals must be certified as: 

A) Compliant with ISO 9001, IS0 14001, ISO 17025, CE, cGMP Production and Testing Methods

B) Independent 3rd Party HPLC /  LCMS Purity Analysis of 99% or higher (unless otherwise stated).

C) Intended for in vitro research use only, not intended for human consumption.

CytoVive® Laboratories LLC maintains limited liability to confirmatory analysis on products indented for research use only and are not intended for human consumption. Any interpretation and use of the test results are the sole responsibility of the researcher. This resource is related to the research compound(s) listed above and media may not be reproduced, in part or in full, without the expressed written approval of CytoVive Laboratories LLC. CytoVive Laboratories LLC bears zero responsibility for any misuse of any research compounds in any and all jurisdictions, and CytoVive Laboratories LLC reserves the right to refuse sale to any individual or entity for reported expressed misuse of any CytoVive Laboratories LLC Products and/or Services.


All CytoVive formative entities maintain the highest level of regulatory compliance (please refer to the CytoVive Standards above. It is the responsibility of any international researcher that places an order from outside of the United States to do their own due diligence with respect to the regulatory status of the compounds they are ordering within the jurisdiction that they intend to receive their order, CytoVive Laboratories LLC does not bear responsibility for any seized or confiscated international parcels. All CytoVive Laboratories LLC orders are shipped within 24 hours and all research compounds are tested to be within the highest quality control parameters (as listed on individual product Certificates of Analysis) with respect to ISO 9001, ISO14001, ISO 17025, CE, and GMP standards. Many of CytoVive Laboratories LLC Products are proudly made in the USA from the purest HPLC /  LCMS lab certified domestic and/or international precursor compounds. We guarantee the highest quality without compromise!

**Medical Professionals Only**

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