You will get American A-I-R-S Number Website & Email Secured Seal
Project details
Register For Website & Email Secured Seal – For just $ 99
Why American IRS Website & Email Secured Seal?
In today’s competitive world, customers are always looking for website & email certification before they make online payments or reply to business emails.
The email seal provided by American IRS can be inserted in every staff official email signature so that the receiver of the email can click on American IRS® email seal and be sure they are dealing with American IRS certified company.
A lot of companies are offering site seals but you can avail website seal from Business Credit Risk Rating Company thus adding a lot of value to your brand.
Get American IRS Website & Email Secured Seal.
Increase customer confidence.
Why American IRS Website & Email Secured Seal?
In today’s competitive world, customers are always looking for website & email certification before they make online payments or reply to business emails.
The email seal provided by American IRS can be inserted in every staff official email signature so that the receiver of the email can click on American IRS® email seal and be sure they are dealing with American IRS certified company.
A lot of companies are offering site seals but you can avail website seal from Business Credit Risk Rating Company thus adding a lot of value to your brand.
Get American IRS Website & Email Secured Seal.
Increase customer confidence.
Project Type
Business Consulting, Financial Consulting, Human Resources, Legal, Training & DevelopmentWhat's included $99
These options are included with the project scope.
$99
- Delivery Time 2 days
- Number of Revisions 1
About Anim Akhtar Ali
USFDA Registration Consultant for Food, Drugs, Cosmetic, All Devices
Mumbai, India - 8:45 pm local time
In today’s competitive global marketplace, compliance is not just a legal requirement—it is a powerful advantage. As a seasoned freelancer specializing in USFDA Registration and Compliance Consulting, I help businesses worldwide navigate the complexities of regulatory approvals across multiple industries. With hands-on experience in Food & Beverages, Pharmaceuticals (Drugs), Cosmetics, Medical Devices, and advanced 510(k) submissions, I provide tailored guidance that accelerates your market entry while ensuring strict adherence to U.S. Food and Drug Administration (FDA) standards.
Why Choose a Freelance FDA Consultant?
Many companies hesitate when approaching U.S. markets due to the perceived cost and complexity of FDA regulations. Partnering with a freelancer like me offers businesses—whether startups or large enterprises—personalized, cost-effective, and transparent support. Unlike large consulting firms that often prioritize volume, I dedicate time and attention to every client, ensuring that your product receives the focus it deserves.
Food & Beverages Registration
The U.S. is one of the largest consumer markets for imported food and beverages. To access it, FDA Food Facility Registration under the Food Safety Modernization Act (FSMA) is mandatory. I assist with facility registrations, Prior Notice filings, labeling compliance, and FSVP (Foreign Supplier Verification Program) guidance—helping exporters maintain trust and credibility in the U.S. market.
Drug Establishment Registration and Listing
Pharmaceutical compliance demands precision. My expertise includes Drug Establishment Registration, NDC (National Drug Code) assignments, and Drug Product Listing in the FDA’s database. From Over-the-Counter (OTC) medicines to prescription drugs, I ensure accurate submissions, minimizing the risk of rejection or delays that could disrupt your supply chain.
Cosmetic Facility Registration and Product Listing
The demand for international cosmetics in the U.S. continues to grow, but regulatory scrutiny has also increased under the Modernization of Cosmetics Regulation Act (MoCRA). I help cosmetic brands achieve FDA Voluntary Cosmetic Registration Program (VCRP) compliance, review ingredient safety, and ensure labeling standards meet U.S. guidelines—supporting faster retail entry and consumer confidence.
Medical Device Registration and 510(k) Submissions
For medical devices, U.S. market access often requires Establishment Registration, Device Listing, and in many cases, a 510(k) premarket notification. I work closely with manufacturers to classify devices correctly, prepare technical documentation, and liaise with FDA reviewers to streamline approvals. My experience spans low-risk Class I devices to complex Class II and III products requiring detailed clinical and performance data.
Global Experience, Local Advantage
Over the years, I have worked with clients across Asia, Europe, the Middle East, and North America, building a strong understanding of how global companies approach FDA compliance. This cross-border expertise allows me to anticipate potential challenges and develop strategies that reduce time-to-market. Whether you are a small exporter in India, a supplement brand in Europe, or a medical device manufacturer in the Middle East, I provide step-by-step guidance tailored to your region’s specific challenges.
End-to-End Services Offered
FDA Facility Registration (Food, Drug, Cosmetic, Medical Device)
U.S. Agent Services for foreign manufacturers
Product Listing & Label Review
Drug NDC Code Application
Device Listing and 510(k) Preparation
Annual FDA Registration Renewal & Compliance Updates
Advisory on U.S. Import Alerts and Detentions
Building Trust Through Compliance
FDA registration is not only about meeting regulatory requirements; it is about building lasting trust with U.S. customers, distributors, and partners. Businesses that demonstrate compliance stand out in competitive markets, gain faster retail approvals, and avoid costly legal penalties. By working with an experienced freelancer, you gain the flexibility of independent consulting with the reliability of global regulatory expertise.
Conclusion
Navigating the FDA system can be overwhelming, but it does not have to be. With years of hands-on experience in USFDA registration and compliance across diverse industries, I provide businesses with the clarity, speed, and expertise needed to thrive in the U.S. market. Whether your focus is food, beverages, pharmaceuticals, cosmetics, or medical devices, my freelance consultancy ensures that your journey to U.S. compliance is smooth, efficient, and future-proof.
Steps for completing your project
After purchasing the project, send requirements so Anim Akhtar Ali can start the project.
Delivery time starts when Anim Akhtar Ali receives requirements from you.
Anim Akhtar Ali works on your project following the steps below.
Revisions may occur after the delivery date.
After completion of payment on Upwork
Once upwork confirms the payment is processed, i will contact you to collection your company registration document and post review the website & email secured seal is issued