Top 10 FDA Consultants in India & USA!

There are thousands of FDA Consultants in India and around the Globe. Some companies or FDA Firms have more than 20 years of experience in business and some are new. Today we are sharing Top 20 Global US, India and Global FDA Consultants who are best in the industry and have more than 10 years of Experience in Business.

I3CGLOBAL is on the first position and have very professional and expert US FDA Consultants for Medical Devices and helping Domestic and Foreign organizations comply with US FDA regulations.

I3CGLOBAL provide quality and regulatory consulting services to drugs, Nutraceuticals, cosmetics, food, medical device organizations regulated by the US FDA. No matter the size and the products manufactured. They have more than 20+ Years of Experience 1200+ Happy Customers 94% Satisfaction

MDI Consultants is a leader in providing FDA consulting services to the healthcare industry worldwide. MDI Consultants is on number 2nd on the list of FDA Consultants. They have extensive expertise in helping medical device, pharmaceutical, biotechnology and food companies achieve compliance with U.S., European and Canadian regulations.

It is the most aim of Ken Block consulting firm to supply the very best quality regulatory and FDA Consultants services to medical device companies worldwide. Ken Block Consulting is committed to providing value, trust, and reference to those we interact with, and our goal isn’t simply to unravel problems but to empower our clients within the process in order that they will affect issues more effectively within the future.

Ken Block Consulting will always protect client confidentiality and can always provide honest and accurate answers. They follow a policy of ethics and transparency with our clients in order that they, in turn, can approach regulatory authorities with the knowledge and confidence necessary to succeed.

Smith Associates (FDA Consultants) can assist small and enormous companies in writing and implementing their Quality System, or enhancing their ISO Quality System to conformance to Part 820. Smith Associates Standard and Operating Procedures, Forms and Work Instructions are implemented, audited and inspected by the FDA and has successfully fulfilled the FDA’s requirements.

If you’re planning on adding additional products to your existing line or are a start-up medical device company you would like to remember of 21 CFR 820.30 Design Control. the present thinking at the Food and Drug Administration is more in-depth inspections of the planning History File documentation (design inputs, design process, and style outputs), Device Master Record (DMR), Acceptance Criteria, Design Review Meeting minutes, verification and validation steps including Risk Analysis (ISO14197), Human Factor Studies, etc. Smith Associates has created a Step-by-Step Standard procedure to help you in meeting the wants of 21 CFR 820.30 from concept and feasibility to final finished product.

Weinberg Group has an expert FDA Consultants and in business from more than 35 years. Weinberg Group company has made sure clients such as you achieve their drug and device development goals. we’ve spent longer deciding what you would like than most firms have spent in business. Along the way, we’ve developed the relationships required to urge your product through to subsequent step.

Their experienced team of Food and Drug Administration consultants and regulatory compliance consultants work with you to develop regulatory strategies and submissions, and remediate, maintain, and improve regulatory compliance.

EAS Consulting Group is a best and leading service provider of Regulatory compliance solutions to industries regulated by FDA, USDA, and supporting agencies. Our team of consultants provide expert guidance for all of your regulatory requirements.

EAS Consulting Group mission is to supply quality regulatory advice and repair and to represent the simplest interests of our clients in an ethical, timely, and cost-efficient manner.

Through our alignment with Certified Laboratories, a number one full-service food testing laboratory servicing the food industry since 1926, Lab stat, a best in school tobacco, nicotine and vape safety laboratory and Labs-Mart, a dietary supplement, vitamin, and healthy products laboratory, EAS can assist you together with your regulatory requirements and challenges, while offering a more robust scope of testing services to satisfy your organization’s sophisticated needs.

FDA Quality and Regulatory Consultants LLC offer Regulatory Consulting for Pharmaceutical, Medical Device and Biotech companies. thanks to the FDA experiences, they offer customized, value-added solutions, processes and enhanced quality standards to optimize business efficiencies and minimize regulatory risk.

At FDAQRC we partner your needs with the perfect Consultant. we’ve over 300 Consultants in our network to make sure we meet your technical requirements. If you’re looking to partner with us you’ll use this online tool to start out the registration process. If you’re already registered with us and would really like to review your profile, please log in.

FDA Compliance Simplified provides development, regulatory compliance and complete labelling services for FDA and USDA regulated consumer products. They work with various industry sectors including dietary supplements, cosmetics, food and beverages also as pet foods, medical devices and over the counter medicines.

They have a network of development and regulatory affairs professionals that has been providing technical and regulatory affairs support services to the biotechnology, pharmaceutical, cosmetic, dietary supplement and food industries since 2001. We are able to assist you and your company succeed.

Pharmaceutical Development Group (PDG) assists FDA regulated firms within the navigation of the U.S FDA submission, approval and post-marketing procedures across a spread of dosage forms and therapeutic areas. the corporate expertise spans prescription and nonprescription (OTC) drugs, both NDA and monograph, also as devices.

They focus our experiences and energies to function your long-term regulatory partner throughout product lifecycles. PDG will develop strategic plans and lifecycle management options designed to maximise the security, efficacy, and commercial value of your products.

FDA Basics LLC, (FDA Consultants) previously referred to as Tobias Systems, started their journey the year 1995. The initial focus was on FDA US Agent services to numerous foreign companies for selling medical devices, drugs, and food products within us. As our experience built, so did our services, to incorporate DMF filings, ANDA/NDA filings, and Establishment Registration, also as a variety of other services associated with FDA compliance. We are now proud to supply expert support that pulls on over twenty years of operation.

They are committed to providing the very best quality services for food, medical device, drug, and cosmetics companies. Our focus is on providing you with the recommendation you would like, not only for regulatory consulting except for your long-term business goals. We pride ourselves in offering expert, cost-effective solutions. we’ve worked with companies large and little, from all around the world. FDAbasics is headquartered in Florida, USA.

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FAQs about FDA Consultants!

How to choose FDA Consultants?

You can choose FDA Consultants by their online reputation, years in business and reviews. Also, check their complete certification before go for services.

Which Company have best FDA Consultants?

In our opinion, you should choose I3CGlOBAL FDA Consulting Firm. They are the best in the industry and have more than 20 years of Experience in Business. The entire team is very Down to Earth especially Mr George. You Can contact them directly on (+91 99 45912081) for Indian FDA Certificate Registraion or Renewal or any other query or consulting regarding regulatory services.

What is the Motive of this FDA Consultants Blog?

This blog is only for Knowledge and Information purpose. We strongly recommend you to check each and every aspect carefully before buying any FDA Consulting Company or Service Provider.

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