2 Industrial Rd Suite 203 Fairfield, NJ 07004
Call: (973) 402-5888
Email: contact@thekentgroup.com
Most safety leaders don’t lie awake worrying about the incident that’s already been reported – they worry about the one nobody’s caught yet; the forklift route that’s technically fine but feels wrong every time someone walks past it, the chemical storage area that’s “been like that for years.” EHS audit services exist for exactly that gap: […]
Every superintendent has a story- a ladder tied off wrong. A trench that looked fine until it didn’t. A subcontractor who assumed someone else was watching the crane’s swing radius. None of these things happen because people don’t care about safety. They happen because on a busy jobsite, with five trades working at once and
Cargo security remains a major concern across the supply chain industry. Companies that move, store, or distribute valuable goods face increasing pressure to protect cargo from theft, tampering, and unauthorized access. This need has made the TAPA FSR inspection in NJ an important standard for warehouses, logistics providers, and cargo facilities. If you are wondering
What Is TAPA FSR Certification? A Complete Guide for NJ & Newark Cargo Facilities Read More »
Houston remains one of the most important industrial hubs in the United States. Its economy depends heavily on energy production, manufacturing operations, and international trade. As companies prepare for 2026, supply chain challenges continue to evolve. Global uncertainty, changing regulations, labor shortages, and quality concerns are creating new pressures across industries. These challenges make supplier
New Jersey has earned a strong reputation as the pharmaceutical capital of the United States. Some of the world’s largest pharmaceutical companies, including Johnson & Johnson, Pfizer, Merck, Novartis, and Bayer, maintain significant operations across the state. The region has developed into a highly connected pharmaceutical corridor that supports research, manufacturing, packaging, testing, and distribution
Food safety remains a major focus for manufacturers, processors, distributors, and hospitality businesses across the United States. Regulatory requirements continue to evolve, making audits a critical part of food safety management systems. As businesses prepare for changing expectations in 2026, understanding food safety audit company in Houston frameworks such as HACCP, FSMA, and GFSI becomes
Food Safety Audit Guide 2026: HACCP, FSMA & GFSI Standards Explained Read More »
As manufacturers prepare for another business cycle, compliance, workplace safety, and operational risk management become major priorities. A thorough year-end compliance review helps organizations identify gaps, verify regulatory adherence, and strengthen internal controls before entering a new year. In industries where supplier performance, operational continuity, and safety standards directly affect production, audits play a critical
EHS Audit Checklist: 10 Critical Areas Every Manufacturer Must Review Before Year-End Read More »
Supply chains have become more complex than ever. Companies depend on multiple suppliers, manufacturers, transportation partners, and distributors to keep products moving efficiently. As a result, auditing has become an essential part of maintaining quality, compliance, and operational performance. One common question organizations face is, “What is the difference between internal and second-party auditing?” Understanding
Second-Party vs. Internal Auditing: Which Does Your Supply Chain Actually Need? Read More »
Manufacturing companies across New Jersey are entering a period of increased regulatory attention. Federal and state workplace safety agencies have announced stronger enforcement efforts, more inspections, and greater scrutiny of safety management systems. As a result, manufacturers must review their safety programs and audit processes before inspectors arrive. Understanding the relationship between internal reviews and
OSHA’s 2026 Enforcement Surge: What New Jersey Manufacturers Must Do Now Read More »
The medical device industry is entering a new regulatory era. The U.S. Food and Drug Administration (FDA) has introduced the Quality Management System Regulation (QMSR), a major update that changes how manufacturers maintain and demonstrate compliance. As the FDA QMSR deadline approaches, companies must understand what the new requirements mean and how they affect existing
FDA’s QMSR Regulation: What Medical Device Companies Must Do Before the Deadline Read More »
