Tag: Current Affairs
The beauty industry is experiencing a regulatory glow-up, thanks to the Modernization of Cosmetics Regulation Act (MoCRA). With the FDA tightening its grip on cosmetics oversight, the impact is being felt not just in the U.S. but across international borders. From import/export compliance to global harmonization efforts, brands navigating this evolving landscape must be prepared […]
What this Means for Regulated Industry
The U.S. Food and Drug Administration (FDA) announced the revocation of Red No. 3 (FD&C Red No. 3) for use in foods and dietary supplements. This decision, which has sparked significant discussion within the regulated industry, marks a pivotal moment in food additive regulation and consumer safety. What is Red No. 3? Red No. 3 […]
A Game Changer for Industry
The Food and Drug Administration (FDA) has officially redefined the term “healthy,” serving us a regulatory receipt that promises to transform the food industry. In a move designed to reflect the latest nutritional science and consumer expectations, the FDA’s new regulations are set to shake up how food manufacturers market their products. Spoiler alert: the […]
Navigating FDA’s New Scombrotoxin Standards
The FDA recently set sail with a new Compliance Policy Guide (CPG) that brings updated standards to the often-complex world of scombrotoxin (histamine) management in fish and fishery products. This regulatory move impacts a wide range of seafood industry players—from fishermen and processors to distributors and retailers—by setting clear standards on how fish prone to […]
The Bewitching World of FDA-Approved Halloween Candy Colors
When you dive into a bucket of Halloween candy, you’re not just snagging sweet treats; you’re reaching into a cauldron of FDA-approved colors, flavors, and ingredients that make those goodies as vibrant as a witch’s wardrobe. Ever wondered why your candy corn is orange or your gummy worms are a little too green? Well, it’s […]
Navigating the FDA’s High Seas of Foreign Supplier Verification Program (FSVP) Inspections
Ahoy, mateys! Batten down the hatches and hold onto your manifests, because the FDA’s on the prowl, issuing Warning Letters like they’re going out of style! If you’re in the business of importing FDA-regulated products, particularly food, you’re probably well aware of the Foreign Supplier Verification Program (FSVP). And if you’re not—well, now’s the time […]
What This Means for the Regulated Industry
FDA announced this week that it will examine the potential harm to women of heavy metals exposure such as lead, cadmium and arsenic found in tampons, following the results of a July pilot study, growing consumer concern over product safety, ingredient transparency, and potential health risks associated with tampon use. FDA stated that while the […]
Navigating FDA’s Complex Regulation of Homeopathic and Ayurvedic Products
In an era where natural and alternative medicines continue to gain traction driven by a growing interest in holistic and natural health alternatives, the U.S. Food and Drug Administration (FDA) finds itself at the intersection of tradition and science. Homeopathic and ayurvedic products, rooted in centuries-old practices, have become a sizeable industry in the United […]
The FDA and FTC recently issued warning letters to several companies involved in the sale of Delta-8 THC products in packaging mimicking popular national brands appealing to both children and adults, reflecting growing regulatory scrutiny over the rapidly expanding market for this cannabinoid. Delta-8 THC, a compound derived from hemp, gained popularity due to its […]
The Magic of FDA Export Certificates Including New Requirements for Dairy Exports to India
U.S. FDA compliance, marketing clearance, and being in general good standing with the Agency is oftentimes the secret sauce to international markets. Foreign governments and foreign purchasers are keen to understand whether and to what extent exported goods comply first with U.S. regulatory requirements, marking a glittery stamp of approval. To help in this effort, […]
★★★★★
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.
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.
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.
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.
