FDA Administration & Regulatory Affairs Expert Witness

FDA Administration & Regulatory Affairs expert witnesses review records, provide opinion and testify at deposition or trial in all types of cases. These may include business administration & regulatory affairs, standard operating procedures, fda regulation compliance, product process optimization, science, and statistics. These may also include regulatory affairs, food companies, dietary supplement, gmp, good manufacturing practice, food processing, preventive controls, or allergen. Additionally, these may also include manufacturing, packaging, inventory control, supply chain, food safety plan, hazard analysis, and contaminant.

Expert FDA Administration & Regulatory Affairs Witnesses’ Review Opinion & Testimony

These FDA administration & regulatory affairs experts also include professionals that have experience in quality management, contract manufacturing, label, product development, document, quality systems, drug formulation in general. They also may have experience in quality management, dietary supplement, medical device, user requirements specification, design development planning, and design input.

Ultimately, the primary goal of the expert is to provide forensic evaluation, deposition or courtroom testimony to opine standards of this industry. Consolidated Consultants has referred experts to both plaintiff and defense attorneys for many years.

Please review the wide variety of expert witnesses and use the "Request This Expert option to contact us. Please review the standard list and select the closest specialty. You can refine your search on the subsequent pages, including search words, location by region, selectable states, and individual states.

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. Medical Device Compliance 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, Covid-19, EUA

3. Pharmaceutical Oncology Expert Witness

Provides Opinion & Testimony In:

Pharmaceutical, New Drug Application Under FDA, Medical Imaging, Oncology, Pain Management, Anti Infectives, Ophthalmics, Drug Development, Drug Identification, Drug Labeling, Drug Labels, Drug Warnings, Drug Safety, FDA Medical Device Regulation, FDA New Drug Review Approval Procedures, Medical Devices, Pharmaceutical Development, Pharmaceutical Process Chemistry, Pharmaceutical Science, Pharmaceuticals, Pharmaceuticals Manufacturing, Pharmaceuticals Regulatory Affairs, Quality Assurance, GXP, GMP, GLP, GCP Compliance, Regulatory Issues, Risk Management, Review FDA Correspondence,

4. Industrial Hygiene Warning Labels Expert Witness

Provides Opinion & Testimony In:

General Industrial Hygiene Safety Issues Warning Labels, industrial hygiene, Health & Safety Standards, OSHA MSHA EPA Regulations Practices, Asbestos General Toxic Torts Litigation Support, Hazardous Exposure Risk Assessment Modeling, Health & Safety Programs, MSDS Warning Labeling, General Forensic Science Litigation Support, Personal Injury Product Liability Litigation Support, Environmental Microbiology,

5. 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

Why CCC?

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Expansive Network of Over 30,000 Experts

100’s of categories of highly-qualified medical and technical experts in just about every state, for just about any type of case.

We’re Trusted in Over 10,000 Legal Cases

Since 1995 we’ve worked with 1,000’s of medical malpractice, personal injury and government cases in every state and region.

We’re Fast – Search for Free

We respond in less than 1 hour. We’ll search for you or search CV’s on our site by keyword, category, state or region – both are free!

 

Quickly Find The Right Expert In 3 Easy Steps

You request an expert or search our site for free.
We schedule a free conference call with the expert.
You decide the right expert for your case.

We respond in as little as 1 hour

Free Expert Witness Search and Recruiting

You’ll pay nothing to have us do the hunting for the perfect expert witness for you. If, for any reason we don’t have the perfect expert in our network, as always, we’ll do the recruiting for free. Since 1995, we continue to expand our network.