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International Regulatory Consulting. For more information call 403-770-1994 or email us

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Regulatory Consulting Request Form

Need Regulatory Consulting, Submissions, Auditing or Training Services like an FDA GMP Audit or a EU CTD ? 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 email us or call 403-770-1994 .

Regulatory Consulting Request Form:
Industry: Please indicate the industry such as Pharmaceuticals, Biotechnology, Medical Devices, Food & Beverages, Cosmetics, Chemicals, Consumer Products, Clinical Trials, etc. )
Urgency :
Location: Please indicate the location of this project(ie, USA, Ireland, Canada, South America, Asia, France, Austrailia, South Africa, Germany, China, Japan, UK, etc.)
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.
Requirements: 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.
Contact Information :
Company or Organization Name:
Name :
Title:
E-mail Address:
Phone Number:
Address:

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