Quality assurance at ScieGen is led by experienced personnel abiding by the best quality norms who ensure that set standards are met. Quality assurance and verification is a companywide function carried out in each and every stage, from receiving to dispatch. Quality assurance personnel are properly trained and equipped with well written procedures, forms and software tools governed by 21 CFR Part 210 current good manufacturing practice in manufacturing, processing, packing, or holding of drugs; General, and 21 CFR Part 211 current good manufacturing practice for finished pharmaceuticals
