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Quality Fda Expert Witness Testimony Service

Quality fda expert witnesses at Consolidated Consultants are available by providing independent opinion as a consultant or as a declared expert by verbal or written report in litigation matters. An attorney typically retains an expert witness to give testimony at deposition or trial in the area of quality fda that is relevant to the case. The following list contains testifying professional experts with special knowledge or proficiency in quality fda.

To see the qualifications of the potential candidate, choose the “View Expert” button. To setup a free conference call screening with an expert witness from the list, simply choose the “Request This Expert” button located in the experts information page.

1. Pharmaceutical Development Risk Management FDA Review Expert Witness

Provides Opinion & Testimony In:

Pharmaceutical Development, Pharmaceutical Scale Up, Instrumentation, Manufacturing, Drug Development, Drug Safety, FDA Medical Device Regulation, 21 CFR Part 11, FDA New Drug Review Approval Procedures, Standard Operating Procedures, FDA Regulation Compliance, Product Process Optimization, Science, Statistics, Pharmaceuticals Regulatory Affairs, Quality Assurance, GXP, GMP, GLP, GCP Compliance, Regulatory Issues, Risk Management, Review FDA Correspondence,

2. Regulatory Marketing Compliance Quality Assurance Medical Device Expert Witness

Provides Opinion & Testimony In:

Regulatory Affairs, Clinical Affairs, Quality Assurance, Regulatory Compliance, Medical Device, Combination Product, Design Dossier, Medicinal Dossier, Director, Client Manager, Project Manager, 510(k),515i, Pre IND, IND, Pre IDE, IDE, HUD, USAN, HDE, PMA, Pre Sub, Recall, Correction, CTA, FDA, CDRH, CE, OUS, MAF, Pre submission, Pre IDE, De Novo, Recall Correction, Appeal, Supplement, Annual report, FSN, FMEA, CER, FSCA, MDEL, MDR, 13485, 10993, 14971, 60601, CMDR, PMS, PMCF, NCA, EFTA, Apostille, legalization, CFG, CFS, QMS, QC, 21 CFR 820, 21 CFR 801, 21 CFR 803, MDL, 21 CFR 807, MEDDEV, NB,
Product Liability, Infringement, Patent Infringement, Injury law,CE, TUV, Intertek, SGS, DGM, NSAI, SNCH, BSI, UL, Medicinal Consultations, MHRA, MPA, ETAT, License Applications, Health Canada, TGA

3. Quality Management Engineering Expert Witness

Provides Opinion & Testimony In:

Quality Management, FDA Compliance certification of medical device manufacturing, Quality systems development, Gap Analysis, Standards Compliance, ISO QS Desk Quality Audits, Process control, Quality Manual, FDA 820 compliance, ISO 9000, ISO 2000 ISO 13485 registration

4. Quality Assurance Medical Standards Medical Billing Expert Witness

Provides Opinion & Testimony In:

Quality Assurance in Medical Standards, Quality Assurance Medical Standards Medical Billing Utilization Review, Board Certified Medical Billing, Insurance Claims Medical Standards of Care, Quality Assurance Medical Standards Medical Billing Coding, Medical Billing, Quality Assurance Medical Standards Medical Billing Managed Care HMO, Medical Over Billing Fraudulent Billing Practices, Quality Assurance Medical Standards Medical Billing, CPT Coding

5. FDA Regulatory Affairs Expert Witness

Provides Opinion & Testimony In:

FDA Regulatory Affairs, Food Drug, Government Regulations, Drug Regulatory Practices, Regulatory Affairs, Initial Product Development, Transfer Of Technology, QA Compliance, Commercial Drug Delivery, Iontophoretic Medical Device Drug Delivery, IND, NDA, ANDA,

6. FDA Regulatory Affairs Professional Expert Witness

Provides Opinion & Testimony In:

FDA Regulatory Affairs Professional, Certified FDA Regulatory Affairs, Regulatory Compliance Quality Assurance Functions, FDA Regulatory Affairs Drug Manufacturers, FDA Regulatory Affairs Equipment Facility Implementation, FDA Regulatory Affairs Quality Assurance, FDA Regulatory Affairs Drug Process Manufacturing Investigation, FDA Regulatory Affairs,

7. FDA Regulations Manufacturing Technology Expert Witness

Provides Opinion & Testimony In:

Regulatory Affairs, FDA Regulations, Quality Systems, Drug Formulation, Quality Management, Dietary Supplement, Medical Device, User Requirements Specification, Design Development Planning, Design Input, Design Output, Design Review, Design Verification, Design Validation, Design Transfer, Pharmaceutical, Validation, Compliance, CAPA, Corrective Preventive Action, Root Cause Analysis, Risk Assessment, Failure Mode Effects Analysis, Fault Tree Analysis, HAZOP, Hazard Analysis Critical Control Points, R D, New Product Development, Calibration, Installation Qualification, Operation Qualification, Performance Qualification, Process Validation, Process Design, Process Performance Qualification, Continuous Process Verification, Statistical Process Control, Stability, Change Control

10. Indoor Air Quality Expert Witness

Provides Opinion & Testimony In:

Chemistry Chemical Engineer Fire Explosion Investigator, Chemical Engineer Engineering, Chemistry, Chemical, Engineering, Fires, Explosions, Origin Cause Fires Explosions, Hazardous Chemicals, Flammable Materials, Products Liability, Household Industrial Products, Accident Reconstruction, Safer Alternatives, Chemical Burns, Toxic Exposures, Flammable Fabrics, Clothing Fires, Clothing Flammability, Analysis Of Hazardous Chemicals, Warnings, Instructions, Labeling, Defective Label Analysis, Patent Infringement Issues, Trade Secret Litigation, Trademark Litigation, Chemical Product Process Issues, Intellectual Property Management, Safety Chemical Product Design Formulation, Safety Packaging Handling, Household Products, Industrial Products, Codes Standards, OSHA Regulations Hair Relaxers, Drain Cleaners, Aerosols, Beauty Products, Cosmetics, Personal Care Products, Silicones, Gels, Flocculants, Coagulants, Water Soluble Polymers, Product Development, Personal Injury,