Our markets
TSG serves a number of key markets and industry sectors including agricultural, industrial, consumer, food and beverage, animal health, and medical. Our team of consultants provide technical and regulatory advisory services in areas that pose challenges to our clients.
Services
We help companies navigate the regulatory landscape across a range of geographies and jurisdictions. Read about the comprehensive range of services we offer.
Agrochemicals
TSG’s agrochemical regulatory consulting services support your business from product innovation through go-to-market. We support producers and distributors of plant protection and health products including pesticides, fertilizers, amending materials, biostimulants, and organic input materials. Our network of regulatory experts, toxicology consultants and scientists help you navigate the international regulatory landscape.

We work with a wide range of government agencies including the US Environmental Protection Agency (EPA), the US Department of Agriculture (USDA), the US Food and Drug Administration (FDA), the European Commission and Member State Competent Authorities in the EU, the Food Safety Authority (EFSA), the European Chemical Agency (ECHA), the Ministry of Agriculture (MOA) People’s Republic of China, the Canadian Pest Management Regulatory Agency (PMRA), and individual US state regulatory agencies.
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Biocides / antimicrobials
TSG’s biocide / antimicrobial pesticide regulatory consulting services support your business from product innovation through go-to-market. Biocide / antimicrobial products cover wide-ranging categories including cleaning products, preservatives and pest control. They are subject to differing and distinctive regulatory approaches depending on geography – so it is important to get the best regulatory support and advice. Our network of regulatory experts, toxicology consultants and scientists help you navigate this complex, international regulatory landscape.

We work with the key regulatory authorities worldwide. In the EU, biocidal products (as opposed to active substances) are authorized at the member state level and TSG’s teams of EU consultants can assist with local authorization. In the US, antimicrobial pesticides are authorized federally under the FIFRA Act and by the EPA with whom TSG engages regularly. We are able to assist with all aspects of product registration and authorization and ongoing maintenance.
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Industrial / specialty chemicals
TSG can help you with all aspects of regulatory and scientific support for industrial and specialty chemicals. Industrial and specialty chemicals constitute thousands of substances which are routinely used in sectors as diverse as automotive, aerospace, food, cosmetics, agriculture, manufacturing, and textiles.

Industrial and specialty chemicals are regulated in the U.S. under the EPA’s Toxic Substances Control Act (TSCA) and in the EU are subject to the Registration, Evaluation, Authorization and Restriction of Chemicals Regulation (EC) No 1907/2006 (REACH). Tens of thousands of chemical substances fall under these regulations. We can assist you with complying with the relevant regulation in the geography in which you are marketing your product.
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Consumer and food & beverage
We provide services to a number of consumer product sectors. These include food & beverage, biocides, cosmetics, personal care, electronics, apparel, and household cleaning supplies.

We can help clients produce safety reports or assessments, develop product information files (PIF), create compliant labels, review formulations, prepare dossiers and provide import/export advice.
Our sister companies also provide a variety of services to the consumer product sectors. Leatherhead Food Research delivers advisory and consumer testing services for food & beverage companies looking specifically at formulation and reformulation checks, claim substantiation, and compliance in different countries globally; whilst Sagentia works with consumer organizations to design and develop smart personal care devices, novel dispensing systems, next-generation baby gear and a range of connected devices for the home.
Medical devices
TSG’s Medical Device Regulatory Consulting team can guide you through all stages of the US Food and Drug Administration’s regulation of medical devices. We can provide FDA regulatory support throughout the lifecycle of the device, including assisting with the determination of the regulatory path, investigational device exemptions (IDE), 510(k) premarket notifications, premarket approval applications (PMA), de novo review submissions, pre-submissions, requests for designation of combination products as devices, 513(g) requests, and post-market compliance for a wide range of devices.

Our sister company, Sagentia Innovation, helps both start-ups and large medical device manufacturers, design and develop ground-breaking devices and technologies.
The leader of TSG’s FDA device regulatory practice also serves as the in-house FDA regulatory advisor to Sagentia Innovation’s medical device product development and advisory teams.
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Professionals
Our regulatory specialists and scientists address all aspects of product registration and ongoing compliance. Read more about the individuals who make up our multi-disciplinary teams.
Services
We help companies navigate the regulatory landscape across a range of geographies and jurisdictions. Read about the comprehensive range of services we offer.