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Socio Platforms Inc
Food & Beverage
US FDA Food Facility Registration (FFR)
US FDA Agent Services
Prior Notice Filing
US FDA Labeling Compliance
Food Safety Compliance (FSMA – Food Safety Modernization Act)
FCE & SID Registration (for Canned / Bottled Foods & Beverages)
Dietary Supplements & Nutraceuticals Compliance
GRAS & Food Additive Consultation
US Importer Assistance (FSVP – Foreign Supplier Verification Program)
USFDA Inspection & Audit Readiness
Product Recall & Enforcement Guidance
Ongoing Compliance Monitoring
Cosmetics
Voluntary Cosmetic Registration Program (VCRP)
Labeling & Claims Review
Ingredient Compliance & Safety Review
Cosmetics GMP (Good Manufacturing Practices)
Import Compliance & Customs Clearance
Product Classification (Cosmetic vs. Drug vs. OTC Hybrid)
MoCRA (Modernization of Cosmetics Regulation Act of 2022) Compliance
Adverse Event & Safety Reporting
Inspection & Audit Readiness
Product Recall Guidance
Drugs
US FDA Drug Establishment Registration (21 CFR Part 207)
Drug Listing (NDC – National Drug Code Assignment)
US Agent Services (for Foreign Drug Manufacturers)
ANDA & NDA Submissions Support
OTC Drug Monograph Compliance
Drug Labeling Compliance (21 CFR 201)
cGMP Compliance (21 CFR Parts 210 & 211)
DMF (Drug Master File) Preparation & Filing
Clinical Trial IND Support
ANDA Bioequivalence Studies Coordination
Controlled Substances Compliance (DEA + FDA overlap)
Import Compliance & Customs Clearance
Post-Market Reporting & Pharmacovigilance
USFDA Inspection & Audit Readiness
Product Recall & Enforcement Guidance
Annual & Ongoing Compliance
Medical Devices
Establishment Registration & Device Listing (21 CFR Part 807)
US FDA Agent Services (for Foreign Manufacturers)
Device Classification & Regulatory Pathway Determination
510(k) Premarket Notification
De Novo Classification Requests
Premarket Approval (PMA) Applications (Class III Devices)
Investigational Device Exemption (IDE)
Labeling Compliance (21 CFR Part 801)
Quality System Regulation (QSR / 21 CFR Part 820)
Medical Device Reporting (MDR / 21 CFR Part 803)
eSTAR & eCopy Submissions
Import Compliance & Customs Clearance
FDA Inspection & Audit Readiness
Post-Market Surveillance & Compliance
Annual & Ongoing Compliance
FDA 510(K)
510(k) Eligibility & Device Classification
Regulatory Strategy Development
510(k) Dossier Preparation
Labeling & Instructions for Use (IFU)
Clinical Data Support
eSTAR / eCopy Submission Formatting
USFDA Communication & Response Handling
Clearance Certificate & Post-Market Setup
Specialized 510(k) Pathways Support
Inspection & Audit Readiness (Post-510(k))
Other Industries
Dietary Supplements & Nutraceuticals
Tobacco & E-Cigarettes (Center for Tobacco Products – CTP)
Animal & Veterinary Products
Radiation-Emitting Electronic Products (21 CFR Parts 1000–1050)
Biologics & Vaccines
Blood & Tissue Products
Human Cells, Tissues, and Cellular/Tissue-Based Products (HCT/Ps)
Veterinary Medical Devices
Color Additives & Food Contact Substances
Infant Formula & Baby Foods
Alcoholic Beverages (FDA + TTB Overlap)
Contact
XPRO Serves Clients in United States
Fill Sales Lead Form
Sales Lead Number - 828638
Investigational Device Exemption (IDE)
What You'll Get
All the steps required for registration are listed below:
Fill out the online registration form.
Enter your information with requirement.
An Account Manager will assigned.
One year of free support.
Enter Company Information
Company Name
*
Country Located
*
Enter Applicant Information
First Name
*
Last Name
*
Mobile Number with Country Code
*
Email ID
*
Message
*
Submit Sales Lead
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