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Google search volume for "510"

Website results for "510"

Page 17 of 186 results

#0 (

0%) - jdconsultingsite.com

Title: FDA Medical Device Regulatory Compliance Consultants, Engineering, Manufacturing Process Validation, Quality/Regulatory Complia

Description: JD Consulting is a medical device consulting firm for regulatory compliance, medical device manufacturing and engineering excellence and process validation.

Keywords:Medical Device Regulatory Compliance, FDA Warning Letter, FDA 483, 510k, Manufacturing Process Validation consulting, Quality/Regulatory Compliance, Manufacturing Problem Solving

#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)

methods improvement, automated process, process control, GMP audit, clinical audit, design control audit, Quality System audit, QSIT, feasibility, due diligence, product development, regulatory strategy, 483 response, Form FDA 483, Warning Letter, consent decree, injunction, recall, MDR, FDA submission, FDA approval, marketing, pre-approval inspection, PAI, preclinical studies, pharmacovigilence, clinical research, clinical study, clinical protocol, statistics, data management, Investigators Meeting, Investigational New Drug, New Drug Application, Abbreviated New Drug Application, Investigational Device Exemption, Pre-market Approval, Pre-market Notification, Master File, IND, IDE, NDA, ANDA, DMF, 510k, PMA, CMC, registration, listing, complaint handling, adverse event, adverse drug reporting, medical device reporting, CAPA, Standard Operating Procedure, SOP, Master Batch Record, Device Master Record, design history file, requirements management, software requirements, software design, design plan, PDP, software validation, change control, verification and validation, software testing, traceability, SRS, electronic records, electronic signatures, ERES, 21 CFR Part 11, 21 CFR Part 820(View Less)

#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.

#0 (

0%) - advancedbiomedicalconsulting.com

Title: Advanced Biomedical Consulting Cost Effective FDA Compliance Consultants - Service Provider to Pharmaceutical Biopharmaceutical

Description: Not available

Keywords:fda, consultants, validation, compliance, DOH licensing, 510k, warning letters, HACCP, Design Control, drug listing, cGMP, QSR, training, medical device, dietary supplements, law, structured product labeling, e-pedigree, pedigree laws, SPL

#0 (

Title: Home

Description: Not available

Keywords:Validation, Training, Qualification, Drugs, Pharmaceuticals, Parenterals, Medical Devices, Biologics, FDA, 483, GMP, GLP, GCP, Biotechnology, Compliance, Quality, Quality Systems, Regulatory, QSIT, PAI, 510k, Adverse event Reporting, ANDA, Auditing, Assessment,

... (View More)

#12,794,092 (

0%) - adviqual.com

Title: Home - AdviQual / en

Description: Quality management consultancy, auditing (mock audits, internal audits) technical training in quality management, process and software validation, clinic evaluation report and dossier preparation services for Medical Device sector.

#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)

510k, Accutane, AFP, Annuloplasty, Apnea monitors, Baycol, Bayesian Methods, Biocompatibility, Biological Indicators, Bioresearch, Bioterrorism, Blue Book, Bone Cement, Bone Densitometer, BSE, Cardiopulmonary Bypass Oxygenators, Catheter, CDRH, Cenestin, CGMP, Chemistry, Cipro, CLIA, Clinical investigator, Clinical Laboratory Improvement Amendments, Clinical trials, Closure integrity, Color additives, Consent decree, Contact lens, Debarment, Device master file, Dialyzer, Dockets, Doxycyline, Drug master file, Drug patent, DSMA, Electroencephalograph, Electromagnetic Compatibility, Electronic Muscle Stimulators, Electronic signatures, Endoscopic Electrosurgical Unit, Endosseous Implant, EtO, Exclusivity, Expiration Dating, Export, FDAMA, Form 3500A, generic, Generic, Germicide, GLP, GMP, Good Laboratory, GRAS, Guidewire, HAACP, Hatch-Waxman, Hazard analysis, Hearing aid, Hemodialyzer, Human Factors, Human subject protection, Immunoglobulins, Import alert, Informed Consent, Infusion Pump, Inspector technical guide, Institutional review board, Intraocular Lens, Investigation operations manual, IOL, IRB(View Less)

#0 (

0%) - emersonconsultants.com

Title: Clinical, Regulatory, Reimbursement Consulting for Medical Devices and Biologics

Description: Emerson Consultants Inc. partners with our clients to achieve their business objectives through integrated Reimbursement, Clinical, Regulatory, and Marketing services through: Strategic reimbursement solutions to ensure positive coverage and payment, Exp

#0 (

0%) - pharmateamusa.com

Title: Pharma Team

Description: Pharma Team USA provides performance improvement services and products that drive efficiencies, reduce cost of goods, improve profitability and harmonize overall operations for pharmaceutical, biotech, and medical device companies. Our offerings focus on

Keywords:pharmaceutical consultant, pharmaceutical consulting firms, biotech consultant, biotech consulting firms, management consulting firms, management consultant, fda consultant, regulatory consulting firms, regulatory compliance, FDA compliance, 21 CFR Part 11, 21 CFR 210, 21 CFR 211, 21 CFR 820, 510K, NDA, ANDA, warning letter, 483, FDA Inspection, medical device, medical device consulting firms, lean six sigma, lean 6 sigma, cost of goods,

... (View More)

#3,459,058 (

-16%) - mdiconsultants.com

Title: FDA Consultants | Medical device consultants & pharmaceutical and Food industry consultants | 510(k)Submissions

Description: A quality assurance, regulatory, clinical consulting firm, mdi consultants provides services to the medical device industry, pharmaceutical industry and food industry and provider of services for U.S. Agent, CE mark, ISO 9000, FDA, Pharmaceutical and qua

Keywords:FDA, ISO, Medical Device, 510k submissions, electronic drug listing and registration, FDA drug listing and registration, electronic listing and registration, ISO 9000, ISO 9001, ISO 13485, CE mark, Quality, Regulatory, electronic drug listing, electronic drug registration, consulting, 510k, 510K, PMA, GMP, MDD, IVDD, HACCP, cGMP, FDA drug listing,

... (View More)

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