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Google search volume for "483"

Website results for "483"

 54 websites found

#15,117,166 (-74%) - qsrhelp.com
Title: Rules - Medical Device Forum
Description: Medical Device Forum. QSR - GMP contracting and consulting services for the medical device industry. Services include regulatory affairs, quality assurance, custom software, and FDA Quality System Regulation help.
Keywords:forum, discussion, FDA, ISO 13485, medical devices, medical device, quality assurance, regulatory affairs, GMP, 510k, QSR, calibration, maintenance, custom, software, Weisenborn, Consultants, Consultant, Consultancy, Consulting, Validation, Good Manufacturing Practices, RA, QA, audits,
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#9,857,632 (-30%) - foiservices.com
Title: FOI Services: Your Source for Unpublished FDA Documents
Description: Document delivery of unpublished FDA information -- pharmaceuticals, medical devices, biologics, veterinary products, all acquired under the Freedom of Information Act.
Keywords:medical devices, pharmaceuticals, biologics, FDA, FOI Services, FOIA, DIOGENES, regulatory affairs, veterinary products, EIR, 483, regulation, drug approval, drug patents, premarket notification, NDA, Freedom of Information Act, Privacy Act, international harmonization, harmonisation, MDR, Food & Drug Administration, documents, 21 CFR, 21CFR,
... (View More)
#0 (0%) - vpcint.com
Title: VPCI - Welcome
Description: FDA regulatory and cGMP consulting services for international pharmaceutical manufacturers.
Keywords:fda, gmp, glp, regulatory consulting, cgmp, validation, protocols, international, italy, spain, switzerland, italian, spanish, english, nda, outlicensing, inlicensing, out-licensing, in-licensing, audit, pai, pre-approval inspection, 483, technology transfer, quality assurance,
... (View More)
#0 (0%) - compliance-insight1.com
Title: FDA Compliance Insight
Description: GMP Training, consultation, guides, SOPs, validation, regulatory and quality.
Keywords:Compliance Insight, compliance, FDA, warning letter, FDA observation, 483, FDA warning letter, audit, cGMP training, GMP, cGMP, FDA audit, GMP training, compliance audit, regulatory, RA, QA, validation, Regulatory Affairs, Quality Assurance, SOP, consultant, FDA consultant, FDA 483


Not available.
#0 (0%) - fdawarning.us
Title: Ingredient Identity - FDA Warning
Description: We provide consulting for FTC actions, FDA Inspection, Form 483’s and Warning Letter responses as well as GMP compliance planning.
Keywords:fda warning, fda warning letters, regulatory consulting, fda inspection, form 483, 483 form, gmp, gmp compliance, 21 cfr, 21 cfr part 111, 21 cfr part 110, 21 cfr part 101


Not available.
#0 (0%) - andregulatory.com
Title: Ingredient Identity - 21 CFR Part 111, FDA, and regulatory, cGMP,
Description: Extensive support for companies needing to comply with 21 CFR Part 111, addressing all areas of quality and regulatory GMP compliance.
Keywords:regulatory consulting, regulatory consulting firm, gmp, gmp compliance, cfr 21, 21 cfr, fda regulations, ndi, gras, gras notifications, regulatory services, fda inspections, form 483, 483 form, warning letter, contract manufacturer, ingredient manufacturers, own label distributors, contract distributors
#8,556,472 (+135%) - regulatory.com
Title: AccuReg® - Serving Developers and Manufacturers of Quality Pharmaceuticals, Biologics, Medical Devices, and Diagnostics Since
Description: Not available
Keywords:Food and Drug Administration, FDA, regulatory affairs, engineering, compliance, medical device, pharmaceutical, prescription drug, over-the-counter, OTC, IVD, Good Manufacturing Practices, GMPs, Quality System Regulation, QS Regulation, QSR, Good Clinical Practices, GCPs, Good Laboratory Practices, GLPs, business process re-engineering, BPR, production equipment, qualification, process analysis,
... (View More)
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