Analytical testing is the process of evaluating and verifying the quality and safety of products in industries such as food, drugs, and cosmetics. It is essential for ensuring compliance with regulations from Health Canada, the FDA, and EFSA. Each regulatory authority has specific guidelines for analytical testing, and understanding how to meet these requirements effectively is crucial for market success.
Analytical testing is mandatory for many products, especially in the food, drug, and cosmetic sectors. Regulatory bodies like Health Canada, the FDA, and EFSA require this testing to ensure that products are safe, effective, and of high quality before they can be marketed and sold to consumers.
Analytical testing is critical for a wide range of industries and stakeholders. If your business operates in any of the following sectors, analytical testing is essential:
Regulatory agencies like the FDA, Health Canada, and EFSA recommend various types of analytical testing to ensure products are safe and effective for use. These include:
Determines the concentration of active pharmaceutical ingredients.
Evaluates how a product’s efficacy and safety change over time under various conditions.
Tests for chemical hazards such as mycotoxins or pesticide residues.
Detects and quantifies microorganisms in food products.
Assesses how well a drug is absorbed and utilized by the body.
Ensures that food products meet nutritional labeling requirements.
Assesses the physical properties of drugs or food products, such as dissolution rates or texture.
Detects residues of pesticides, heavy metals, or other contaminants in food products.
Verifies that food products are genuine and not fraudulent.
Analytical testing is a complex, resource-intensive process that demands specialized scientific expertise, advanced statistical analysis, and a deep understanding of regulatory guidelines from authorities like Health Canada, the FDA, and EFSA.
With over 18 years of experience and a proven track record of helping more than 2,000 brands achieve regulatory approval, GRAS experts are here to provide the precise support you need. We guide you through every step of the testing process, helping you secure final approval and achieve your business growth goals.
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Analytical testing provides crucial data to support food safety audits by identifying potential contaminants, verifying compliance with safety regulations, and confirming the quality of ingredients. This process ensures your product is ready for regulatory approval and meets standards set by authorities like the FDA, EFSA, and Health Canada.
This process plays a vital role in ensuring food products meet the standards set by regulatory bodies like EFSA, FDA, and Health Canada. For FDA compliance, it supports GRAS certification by providing critical safety and toxicology data. For EFSA, it ensures compliance with European food additive regulations and ingredient approval requirements. For Health Canada, testing confirms that food additives and ingredients meet safety standards, align with food additive submission requirements, and comply with Canadian labeling laws. Analytical testing also helps businesses adhere to food safety and quality assurance certification standards globally, reducing the risk of regulatory delays.
Analytical testing ensures the safety and efficacy of food additives and preservatives by evaluating their chemical composition, verifying intended functionality, and detecting contaminants. These tests confirm compliance with food safety standards in the EU, U.S., and Canada.
Yes, GRAS compliance services streamline analytical testing by preparing safety evaluations and regulatory documentation for GRAS ingredients. This ensures a seamless process for demonstrating compliance with international safety standards.
Analytical testing ensures compliance with labeling regulations by verifying the accuracy of nutritional claims, allergen declarations, and ingredient compositions. This data helps businesses meet food safety and quality assurance certification standards while avoiding potential regulatory issues related to false or incomplete labeling.
This process helps identify potential risks early in the product development cycle, such as contamination or formulation inconsistencies. By addressing these issues proactively, businesses can reduce the likelihood of safety concerns during regulatory reviews or food safety audits, streamlining the path to market.
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