Regulatory Consulting Submission Form

Need Regulatory Consulting Services? Simply, complete the form below. Your Regulatory Request will be posted annonymously in our Regulatory Requests Database. If consultants can meet your needs, they will request your contact information which we will forward. If you wish to remain annonymous, simply indicate "Confidential" in the Requirements and we'll send you their contact information. Your confidentialty will be maintained. If you require assistance, please Contact us or call Toll-Free (877) 843-5251.

Please indicate the industry such as Pharmaceuticals, Biotechnology, Medical Devices, Food & Beverages, Cosmetics, Chemicals, Consumer Products, Clinical Trials, etc. )
Please select Urgency.
Please indicate the location of this project(ie, USA, Ireland, Canada, South America, Asia, France, Austrailia, South Africa, Germany, China, Japan, UK, etc.)
Please provide Description.
Please briefly describe the regulatory services or products needed such as FDA NDA Submission, EU CTD, FDA GMP Vendor Audit, ISO Compliance, Expert Witness, Validation & Qualification, Import/Export, Registered Agent, Labeling and Advertising Reviews, Quality Systems, SOP Writing, Pharmacovigiliance, Process Development, Technology Transfer, Training, Regulatory Filings, Part 11, Electronic Records, Clinical Monitoring, etc.
Please specify any experience, knowledge, requirements, education, languages or certfiictitons needed for your project, if any. Please also indicate whether you wish your contact information and company to remain Confidential.
Please provide Company / Organization Name.
Please provide Name.
Please provide Title.
Please provide valid Email.
Please provide Phone Number.
Please provide Address.
For more information, please contact Global Regulatory Inc. at Toll-Free 1-877-843-5251 or email us

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