International Regulatory Resources

Please check this section frequently as much more Regulatory Resources such as guidelines, guidance documents, checklists, forms, books, journals, presentations, blogs, podcasts, templates, etc will be added. For more information , please e-mail us or call 1-1-877-843-5251.
Feature Legal and Regulatory Resources
Legal and Regulatory Resources
Regulatory Books Regulatory and quality reference books related to industries such as the pharmaceuticals. medical devices, biotechnology, healthcare, life sciences, food and beverage, clinical trials, cosmetics, biopharmaceutical, and nutraceutical industries.
Regulatory Periodicals Regulatory and quality journals, magazines, and other publications related to industires such as the pharmaceuticals, biotechnology, food and beverage, nutraceutical, clinical trials, cosmetics, biopharmaceutical, medical devices, and healthcare industries.
Tables Reference tables, blood values, periodic table, MSDS
Equations, Conversion Factors, Constantsscientific and technical conversion factors, equations, and formulae, constants
Regulatory Expert Exchange Forums
Coming Soon. Global Regulatory .com's Experts Exchange Forums features Regulatory, Quality, Compliance Tips, Podcasts, Videos, Abstracts, Templates, Checklists, Procedures, Presentations, Questions and Answers, Articles and Case Studies on topics such as US Food and Drug Administration, Health Canada, EMEA, TGA, Good Manufacturing Practices GMP, ISO, Outsourcing, Quality Systems, Licensing, Certifications, Training, Purchasing, Submissions, Product Development, Technology Transfer, Documentation Control, Quality Control, Recordkeeping, Manufacturing, Bioprocessing, Sterilization, Packaging, Labeling, Research and Development, Distribution, Marketing, Import/ Export, Regulatory Affairs, Good Laboratory Practices GLP, EMEA, Project Management, Good Clinical Practices GCP, Design Controls, Validation, Clinical Monitoring, Clinical Trial Development, Software Validation, Part 11, , EU Directives, CE Marking, Common Technical Documents related to the pharmaceuticals, medical device, healthcare, biotechnology, life sciences, food and beverage, clinical trials, cosmetics, nutraceuticals industries.
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Find attorneys, quality consultants and regulatory consultants in the pharmaceutical, healthcare, medical devices, in-vitro diagnostic, chemical, biopharmaceutical, clinical trials, personal care, veterinary medicine, life sciences, food and beverage, in-vitro diagnostics, biotechnology, dietary supplements, veterinary drugs, and cosmetics industries for USA, Canada, European Union, Asia, Japan regulatory consulting, submissions, training, compliance, expert witnesses, scientific reviews, certifications, guidance, validation, technical writing, export, import, labeling reviews, and audits such as US FDA, GMP, GLP, GCP, ISO, EMEA, Health Canada, TGA, IVDD, MDD compliance, PMA, NDA ANDA submissions, ICH GCP, GMP audits,etc.

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Oxidative Stress Assessment at Kronos Science Laboratory
Submitted by:Kronos Science Laboratory
Extensional Rheometry
Submitted by:Cambridge Polymer Group inc
Bringing medicinal products to market in The European Union (EU)
Submitted by:Pharmalink Consulting Inc
HERBAL MEDICINAL PRODUCTS: Quality, Safety and Efficacy considerations
Submitted by:Pharmalink Consulting Inc
"Future Trends of the GMP's in Japan - based on ICH Guidelines and related activities",
Submitted by:Expert Validation Consulting, Inc.
A Practical Guide to Applying Impact and Risk Concepts to
Submitted by:Expert Validation Consulting, Inc.
Submitted by:Expert Validation Consulting, Inc.
Top 10 Tips for Safely Handling and Using Gas Cylinders
Submitted by:A. Cafferty, Scott Gas
Abstract Presented at the 5th Meeting of the European Society for Chlamydial Research
Submitted by:IBT Reference Laboratory
Are Chlamydia pneumoniae and Mycoplasma pneumoniae Important Etiological Agents of Respiratory Tract Infection in a Family Practice Setting?
Submitted by:IBT Reference Laboratory