May 04, 2022

Public workspacePROTAC GMP Services

DOI
https://dx.doi.org/10.17504/protocols.io.5qpvobq7zl4o/v1
PROTAC GMP Services
  • boc.protac 1
  • 1BOC Sciences
  • PROTAC
boc.protac
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DOI: https://dx.doi.org/10.17504/protocols.io.5qpvobq7zl4o/v1
External link: https://ptc.bocsci.com/services/protac-gmp-services.html
Protocol Citation: boc.protac 2022. PROTAC GMP Services. protocols.io https://dx.doi.org/10.17504/protocols.io.5qpvobq7zl4o/v1
License: This is an open access protocol distributed under the terms of the Creative Commons Attribution License,  which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
Protocol status: Working
We use this protocol and it’s working
Created: May 04, 2022
Last Modified: May 04, 2022
Protocol Integer ID: 61940
Keywords: fda guidelines for gmp manufacturing, protac gmp services boc science, gmp product, releasing gmp product, protac drug discovery, gmp products industry, gmp manufacturing, releasing gmp products industry, gmp manufacturing capability, gmp production site, gmp, grade ligand, software tools for ligand design, performance liquid chromatography, numerous purification option, liquid chromatography isolation, such as liquid chromatography isolation, screening standard qc test, competitive pricing numerous purification option, fda inspection, silica gel purification, ligand, fda guideline, purification, ligand design, drug discovery, standard qc test, fda, protac, boc science
Abstract
BOC Sciences’ GMP production sites were designed in strict accordance to US-FDA guidelines for GMP Manufacturing. It has passed US-FDA inspections. We provide standard QC tests before releasing GMP products. For GMP products, we guarantee >98% purity. In addition, extra tests can be provided according to the requests of clients. Our GMP manufacturing capabilities are designed to meet actual and future customer needs in respect of all stages of PROTAC drug discovery.

Advantages
  • Strategic variety encompassed in the combinations of linkers and ligands aids the design of target degraders
  • State-of-the-art techniques and software tools for ligand design and screening
  • Standard QC tests before releasing GMP products
  • Industry-leading turnaround times on deliveries worldwide-and highly competitive pricing
  • Numerous purification options, such as liquid chromatography isolation, silica gel purification, and high-performance liquid chromatography
  • Both research-grade or GMP-grade ligand and linker can be customized.
  • cGMP Manufacturing that is fully traceable