ORC Expert Advisory Services ORC International

  home    |    find an expert    |    request an expert    |    join our network    |    about us     expert login  
Expert Consulting and Expert Witness Services
  search tips 
Share this page:  Send to LinkedIn Send to Facebook Tweet This Email Print

Related Expert Areas


Food and Drug Administration CFR-21 part 175


21 CFR Part 11


OSHA 29 CFR 1910.146


40 CFR Part 160 FIFRA Final Rule


OSHA 29CFR 1910.1030


Code of Federal Regulations


chromatography applications


employee protection


Food and Drug Administration National Drug Code


Food and Drug Administration compliance


Occupational Safety and Health Administration lead standard


Food and Drug Administration validation


OSHA product labeling


OSHA labeling


Food and Drug Administration drug registration


OSHA ventilation regulation


confined space safety


food processing plant


food processing good manufacturing practice


Occupational Safety and Health Administration standard


OSHA 29CFR 1910.95


adhesive material


Food and Drug Administration


plastic material


food packaging plastic

>> More Expert Areas

'CFR' Experts

To improve your results, click a Related Expert Area on the left.

Experts Only

Join our distinguished experts for CFR jobs, projects and consulting opportunities.

1 to 25
(of 128)
CFR Experts
Request Free
Expert Quote

Expert in Pharmaceutical Technology, Scale-up, Wet granulation end-point, Tableting, Compaction
Expert has 25 years experience in pharmaceutical process scale-up, wet granulation end-point determination, compaction and tableting. He has published many articles on these topics, edited "Pharmaceutical Process Scale-up" handbook, and wrote chapters in ... See full profile

New Jersey (NJ), USA

Expert in Regulatory Affairs, Technology Management, Pharmaceutical Industry, Turnaround Management
Expert has experience in applying 21 CFR Part 11 to the manufacturing of pharmaceuticals and preparing and facing FDA inspections. He has more than 20 years of experience in various facets of API industry ranging from research to manufacturing, ... See full profile

Maharashtra, India

Expert in Pharmaceutical/Biotech Clinical Trials, Regulatory, R&D, Mergers & Acquisitions, Trends, Outsourcing
Expert is Director of Regulatory Affairs and Clinical Trials managing $3.6 billion at at a pharmaceutical company in New York, NY. His expertise is in managing and deploying outsource/insource teams worldwide for multiple clinical trials and ... See full profile

Michigan (MI), USA

Expert in Regulatory Requirements for Food Additives, Color Additives and GRAS Substances
While some sugars and sugar alcohols maybe produce synthetically (at least in part), the term artificial sweetener is ordinarily applied to the intensely sweet synthethic additives: aspartame, acesulfame potassium, sucralose. saccharin, and neotame. See full profile

Michigan (MI), USA

Expert in Medical Device Regulatory Affairs, Quality Assurance, FDA 820 EU ISO 13485 510(k) & Medical Software
Lead and developed regulatory plan and strategy for Molecular Diagnostic System. Blood Analyzer, Gene Profiling Reagents, Blood Analyzer etc. Assembled with team regulatory submission and obtained 510(k) clearance, EU CE Mark, Health Canada, China SFDA, ... See full profile

California (CA), USA

Expert in Medical Device Software, Medical Device Software Engineering, FDA Compliance, FDA 501K and PMAs
Expert has wide range of extensive hands on experience developing and manufacturing medical devices. Over the last twenty plus years he has successfully deployed several medical devices in the cardiovascular, opthalmic, and diagnostic industries. See full profile

California (CA), USA

Expert in Quality Assurance, Regulatory Affairs, Marketing and Business Strategy for Life Sciences Industry
He has performed compliance audits to 21 CFR Part 11. He has developed qualification protocols to test systems compliant with 21 CFR Part 11. He has developed advertising campaigns, written copy for advertisements and managed the creative development of ... See full profile

Montana (MT), USA

Expert in Potato Processing, Vegetable Drying
Expert has 40 years of experience in the potato processing industry, including all phases of production management, quality assurance, research, and development. He is also familiar with numerous potato products, including all types of ... See full profile

Washington (WA), USA

Expert in Cleanrooms, Contamination Control, Ultrapure Media, Qualification and Validation, GMP, AMC
Expert has been active in aersol physics for more than 25 years. His PhD covers also the areas of environmental, indoor and cleanroom aerosols. He worked in a variety of scientific and technical projects covering the health effects of particles to the ... See full profile


Expert in Expert for UL Certification CE Mark NFPA Hazardous Locations Elec. Codes: Get Your Certification NOW
Ul Certification. UL listed equipment and systems Underwriter's laboratory is a preeminent nationally recognized test lab. The United States. Expert will support you in obtaining UL listing and or certification for your products, by managing the whole ... See full profile

Texas (TX), USA

Expert in Health Conditions for International Trade in Fisheries Products, Food Safety, and EU Fisheries
Expert has worked in the Instituto Nacional de Pesca of Ecuador, developing industry codes of practice for processing and handling of farmed and wild-caught shrimp and shrimp products. Assisted with the design and implementation of ... See full profile


Expert in Pharmaceutical Chemical Process R&D, Manufacturing, Disaster Recovery, Software Design
As the IT Manager for a major pharmaceutical company Expert has expertise in selection and validation of document management systems, inventory control, instrument calibration systems, as well as computer software utilized in the pharmaceutical ... See full profile

New York (NY), USA

Expert in GMP Compliance EPCMV of BioPharmaceutical Process, Clean Utilities, Systems, Facilities Engineering
He is a Health Canada Expert (in 2007) and a Senior BioProcess Engineer & Project Manager Consultant; He acquired more than 21 years' experience with various BioPharma Industries & Consulting companies (SNC Lavalin Pharma), where more than 50 projects ... See full profile

Québec, Canada

Expert in Construction Safety
Expert has over 40 years on worldwide professional safety work experience as a Corporate Safety & Security Director for four Engineering, Design & Construction Management Firms, involving over 600 worldwide construction projects, and as a independant ... See full profile

Alabama (AL), USA

Expert in Analytical Chemistry: HPLC, LC-MS, Bioanalysis. R&D projectmanagement; writing of publications
Expert's scientific expertise includes the development, optimization and validation of quantitative bioanalytical methods for small molecules, peptides and biopharmaceutical drugs as well as for their metabolites in biological fluids (plasma, urine, ... See full profile


Expert in Comprehensive Risk Management, Safety, OSHA Compliance, Construction, Manufacturing
Expert has extensive risk management and environmental, safety, and health experience assisting a wide variety of companies and organizations. Expert is a highly respected educational and motivational speaker and trainer, and provider of expert witness ... See full profile

Illinois (IL), USA

Expert in Architecture, Interior Design, Furniture, Landscaping, General Contracting, Safety, Lighting
Expert is a multi-disciplined professional practitioner and court qualified expert in property design, safety, improvements, additions, restoration, damages, defects, failures, injury, liability, codes and interior design, furniture, fixtures, ... See full profile

California (CA), USA

Expert in Occupational Safety and Health, Hazard Recognition/Abatement, Citation Resolution, OSHA/MIOSHA,
Expert is currently the Director of an safety consultanting firm and is providing safety and health services which include audits/surveys with a written description of hazards and safety/health training on the specific hazards found in the work place. See full profile

Michigan (MI), USA

Expert in Validation
Expert has been an independent Validation Consultant for around 10 years; he is responsable for the management of validation projects. He supervises resources acting as a project manager and is also responsible for the development and execution of ... See full profile

Puerto Rico

Expert in Chemical Process Safety Management, Plant Protection, Risk Management, Chemical Plants
He has hands on 25 years experience in design, project execution, commissioning and operation in chemical process industries which includes fertiliser, petrochemical, bulk drugs, fine chemicals, petroleum, oil & gas plants. See full profile


Expert in Public Safety, Occupational Health and Safety, Industrial Training and Course Development
A Workplace Accident and Injury Reduction Program, Expert has worked in the field of Accident Investigation for many years giving him the opportunity to research and establish sound reduction programs for various businesses. Expert has the ability to observe ... See full profile

Missouri (MO), USA

Expert in FDA Regulations, GMP/GLP/GCP Compliance; IND, NDA, BLA, PMA and Product Regulation; Toxicology
Experienced in all aspects of validation and compliance including, GMP/GLP/GCP and part 11. Expert worked for over five years as a reviewer of investigational new drug applications, marketing applications, developing guidance and government policy and ... See full profile

California (CA), USA

Expert in Food Packaging, Food Safety, Food Quality, Food Additives; FDA Compliance, Dairy, JECFA, WHO & FAO
Food packaging; food chemistry; food safety. Expert is an expert in food packaging technology, materials, processes, packaging migrants, and toxicology. His primary area of expertise lies in the overlapping relationships ... See full profile

New York (NY), USA

Expert in Regulatory Sub. NDS, ANDS, SANDS, NC, Cross References, Natural Health Products, Medical Devices
Expert's firm has extensive expertise in regulatory submission. They provide different regulatory strategies to their customer's and prepare all types of submissions on their behalf. Expert also has extensive expertise in Narcotic's regulations. See full profile

Quebec, Canada

Expert in Orphan Drugs: FDA/EU/Canada; FDA Approval; Drug Development: CMC, QA, QC, Manufacturing
12 product approvals from FDA including 6 new chemical entities, a 510k device, and three major pharmaceutical efficacy indication supplemental approvals. All received 5-10 years of regulatory exclusivity (Hatch-Waxman, Orphan Drug). See full profile

Minnesota (MN), USA

>> Next 25 Experts

Need the right expert in CFR?  We can help!

home       find an expert       request an expert       join our network       about us

Intota is now ORC Expert Advisory Services