Regulatory Request Form
Need
Regulatory Consulting, Submissions, Auditing or Training Services like an FDA GMP Quality System , FDA NDA or a EU CTD ? Save Time and Money Searching! Simply,
complete the form below. Your Regulatory Request will be posted
annonymously in our Regulatory Requests Database. If Companies 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 r 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
:
Within the next 24 hours
Within the next 2 - 3 days
Within the next 3 - 5 days
Within the next 5 -7 days
Within the next 2 weeks
Within the next month
Within the next 6 months
Within the next year
Select 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 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 certifications needed, 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:
