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Category: Facility Registration

Avoid Blushing and Don’t Let GMP Violations Add to Your Highlight

09/20/2023

Prepping for a MoCRA and FDA Cosmetics Inspection In a recent News & Insights publication, we addressed FDA’s significant inspection increase, including top citations for each product category, and what to expect and how to prepare for an FDA routine surveillance inspection. With the implementation of the Modernization of Cosmetics Regulations Act of 2022 (MoCRA) […]

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FDA Inspections on the Rise

09/07/2023

What to Expect and How to Prepare FDA’s renewed focus on foreign and domestic inspections via onsite routine surveillance inspections, unannounced inspections and remote regulatory assessments continues to climb across all FDA-regulated industries. Following a pandemic pause, foreign inspections are particularly on the rise with an estimated 1,636 facilities already investigated this year following a […]

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Cosmetic Facility Requirements: Ensuring Product Manufacturing Success

07/20/2023

Are you considering starting your own cosmetic product manufacturing facility? To ensure successful production and compliance with industry standards, it’s crucial to understand the specific requirements for such facilities. From regulatory compliance and facility design to quality control and employee training, this blog post will guide you through the essential aspects of establishing a cosmetic […]

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Mid-Summer Grillin’! Fire up the…Cell Incubator?

07/13/2023

FDA and USDA Regulatory Updates on Lab Grown Meat Summer is synonymous with time at the beach, popsicles and grilling. But soon enough, you may be picking up cell-grown meat on your next grocery run. The U.S. Department of Agriculture (USDA) recently approved two companies, Good Meat and Upside Food, to sell lab-grown and cell-cultivated […]

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FDA Food Allergen Labeling and Cross-Contact

05/25/2023

A Look at FDA’s Enforcement Policy on Major Food Allergen Labeling and Cross-Contact

Update to FDA’s Enforcement Policy on Major Food Allergen Labeling and Cross-Contact As FDA recalls related to allergen labeling continue to abound, and as the agency continues to receive reports of consumers who experienced adverse reactions following exposure to an allergenic substance in foods, FDA provided a much-needed update with its issuance of an updated […]

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Three Cheers for FDA Food Facility Registration Renewal

09/22/2022

It’s that time of year again

Every even-numbered year, food facilities that are required to register with the FDA, must renew their registrations during the period beginning October 1 and ending December 31. Failure to renew a registration by 11:59PM on December 31, 2022 will result in a different kind of excitement New Year’s Eve – your registration will be considered […]

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★★★★★

Working with Shelly on various new product launches over the last couple of years has been seamless. Quick and clear guidance is always what we get.
R.G. Client
I've been working with Shelly and her team at Garg law for a little while now and they are fantastic! Very responsive, professional and they certainly get things done. Extremely satisfied with their service and highly recommend.
Mike H. Client
Ms Garg helped my company navigate an FDA import issue. She achieved an excellent result, was very responsive and professional, and managed to keep the project within budget. She is a stellar attorney.
Dr. Sastry Client
I have been using Shelly Garg as FDA Counsel for 10+ years, since she was at another international law firm. While we continued to use the previous firm she was at (mainly due to the process required to change firms), we realized the quality of counsel was not the same. We have since been using Garg Law and the ease of use and trust in the knowledge was back instantly. Shelly has the skills to help me understand the regulations (by translating into layman's terms) and risks in a manner that is specific to my business. She is also extremely timely in her responses which is critical when we have a deadline mandated by the FDA. Many other attorneys cite the regulations which l've already read, but need further counsel. In my opinion, this demonstrates Shelly's in-depth knowledge of the regulations, how they pertain to the law, and how they are applicable IRL. Shelly's personable approach and pleasant manner in communication makes it very easy to have been work with her and have productive discussions on the best next steps. She truly has a passion iternational for all things FDA and I've learned so much from her.
Claire P. Client

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