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Jecho,
Inc.
provides consulting services, in both technical and regulatory aspects, to manufacturers of biopharmaceuticals. With our extensive scientific knowledge and industrial experiences in protein, peptide,
antibodies, DNA, vaccine, antibiotics, and etc., we work with our clients in process development and cGMP manufacturing that is compliant with FDA regulations. The consultation services
offered by Jecho include technical design and troubleshooting in the areas of process development and GMP manufacturing, documentation
preparation (SOP, CMC/IND, production batch records, DMF), feasibility report, and literature review package preparation.
Jecho, Inc. has access to state-of-art manufacturing facilities and offers contract manufacturing services in GLP and GMP production of bioproducts for animal studies and clinical trials
(Phase I and II).
Jecho, Inc. provides services to clients with proprietary technologies in preparation of technology transfer packages.
Jecho, Inc. provides cGMP training on a variety of topics including quality management system, bioprocess development and validation, quality control and quality assurance, and GMP manufacturing.
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