|GMP-IFGH24||GMP Human IFN-gamma Protein|
|GMP-L02H14||GMP Human IL-2 Protein|
|GMP-L06H27||GMP Human IL-6 Protein|
|GMP-L07H24||GMP Human IL-7 Protein DMF Filed|
|GMP-L15H13||GMP Human IL-15 Protein DMF Filed|
|GMP-L21H25||GMP Human IL-21 Protein DMF Filed|
|GMP-MC0323||GMP Monoclonal Anti-Human CD3 Antibody (OKT3) DMF Filed|
|GMP-MC2824||GMP Monoclonal Anti-Human CD28 Antibody DMF Filed|
|GMP-TNAH23||GMP Human TNF-alpha Protein|
|GMP-NUES19||GMP GENIUS™Nuclease DMF Filed|
|CRS-A024||resDetect™ Human Interleukin-15 (IL-15) ELISA Kit (Residue Testing)|
|CRS-A025||resDetect™ Human Interleukin-7 (IL-7) ELISA Kit (Residue Testing)|
|CRS-A003||resDetect™ Human Interleukin-2 (IL-2) ELISA Kit (Residue Testing)|
|CRS-A005||resDetect™ Human Interleukin-6 (IL-6) ELISA Kit (Residue Testing)|
|CRS-A010||resDetect™ Human Interleukin-21 (IL-21) ELISA Kit (Residue Testing)|
|CRS-A014||resDetect™ Anti-CD28 Antibody ELISA Kit|
|CRS-A015||resDetect™ Anti-CD3 Antibody ELISA Kit|
|CRS-A016||resDetect™ GENIUS™ Nuclease ELISA Kit (Residue Testing)|
ACROBiosystems GMP grade products are produced under a quality management system and in compliance with relevant guidelines: Ph. Eur General Chapter 5.2.12 Raw materials of biological origin for the production of cell-based and gene therapy medicinal products; USP <92> Growth Factors and Cytokines Used in Cell Therapy Manufacturing; USP <1043> Ancillary Materials for Cell, Gene, and Tissue-Engineered Products; ISO/TS 20399-1:2018, Biotechnology - Ancillary Materials Present During the Production of Cellular Therapeutic Products.
ACROBiosystems Quality Management System Contents：
ACROBiosystems provide rigorous quality control tests (fully validated equipment, processes and test methods) on our GMP grade products to ensure that they meet stringent standards in terms of purity, safety, activity and inter-batch stability, and each bulk QC lot mainly contains the following specific information:
ACROBiosystems GMP grade products are designed for research, manufacturing use or ex vivo use. CAUTION: Not intended for human in vivo applications.
All products are warranted to meet ACROBiosystems Inc.’s (“ACRO”) published specifications when used under normal laboratory conditions.
ACRO DOES NOT MAKE ANY OTHER WARRANTY OR REPRESENTATION WHATSOEVER, WHETHER EXPRESS OR IMPLIED, WITH RESPECT TO ITS PRODUCTS. IN PARTICULAR, ACRO DOES NOT MAKE ANY WARRANTY OF SUITABILITY, NONINFRINGEMENT, MERCHANTABILITY OR FITNESS FOR ANY PARTICULAR PURPOSE.
NOT WITH STANDING ANY OTHER PROVISIONS OF THESE TERMS AND/OR ANY OTHER AGREEMENT BETWEEN ACRO AND PURCHASER FOR THE PURCAHSE OF THE PRODUCTS, ACRO’S TOTAL LIABILITY TO PURCHASER ARISING FROM OR IN RELATION TO THESE TERMS, AN AGREEMENT BETWEEN THE PARTIES OR THE PRODUCTS, WHETHER ARISING IN CONTRACT, TORT OR OTHERWISE SHALL BE LIMITED TO THE TOTAL AMOUNT PAID BY PURCHASER TO ACRO FOR THE RELEVANT PRODUCTS. IN NO EVENT WILL ACRO BE LIABLE FOR THE COST OF PROCUREMENT OF SUBSTITUTE GOODS.
The End User is aware that ACROBiosystems Inc. and its affiliate (“ACRO”) sell GMP grade products designed for research, manufacturing use or ex vivo use and not intended for human in vivo applications. The End User further agrees, as a condition of the sales of ACRO’s GMP grade products that: a) the End User will not use this GMP grade product in any procedure wherein the product may be directly or indirectly administered to humans, unless the End User has obtained, or prior to their use will have obtained, an Investigational New Drug (IND) exemption from the FDA and will use the product only in accordance with the protocols of such IND and of the Institutional Review Board overseeing the proposed research, or b) the End User will use the products outside of the United States in accordance with the protocols of research approved by the applicable review board or authorized ethics committee and regulatory agencies to which the End User is subject to in their territory.