our quality

Our Quality Assurance Program

Since our beginning, NJ Labs (New Jersey Laboratories) has earned a reputation for quality and integrity by providing our clients with accurate and reliable chemical & microbiology testing services. NJ Labs has a Quality Assurance department responsible for maintaining a comprehensive and effective Quality Assurance Program, ensuring that data generated by our laboratories are scientifically valid, defensible, and within known acceptable parameters of accuracy. Quality at NJ Labs means full compliance with all requirements. Every aspect of our Quality Assurance Program is designed to ensure that client and regulatory requirements are met. The objectives of our Quality Assurance Program (QAP) are to:

• Define both client and regulatory requirements
• Train our staff to meet both sets of requirements
• Monitor our performance for adherence to requirements
  

Our QAP includes a quality assurance manager, quality assurance documentation, a strong training program, quality assessments, GMP audits, and a corrective action process. The Quality Assurance program is managed by the QA Manager who reports directly to the CEO.

All manufacturers of finished products, packaging, and raw material ingredients are required by law to adhere to strict compliance testing requirements.  Yet, the FDA often finds deficiencies in laboratory testing procedures that cut corners or are otherwise lacking transparency – leading to potential violations of compliance law.  Such oversights can potentially cost customers millions in submission delays, approvals, product recalls or manufacturing interruptions.

NJ Labs got its start in 1936 by promoting quality in dairy & food production and over time as we’ve expanded to other industries, we’ve also been building a culture of quality ever since.  We are certified by the US Food & Drug Administration, the Drug Enforcement Administration, and New Jersey Controlled Substances and we are unique in our broad range of industry expertise.   We know how to work with the FDA but more importantly, how to conduct ethical analytical testing under strict CGMP requirements that comply with regulatory law.