Overview
For the rigorous analysis essential for herbal product registration with the Food and Drugs Authority (FDA), the Centre for Plant Medicine Research in Mampong-Akwapim stands as the foremost authority. Our institution is renowned for its meticulous approach to laboratory examinations, ensuring that all submitted products undergo thorough scrutiny to meet the highest standards of quality and safety.
Every product that reaches our laboratories undergoes a detailed and comprehensive analysis, encompassing various parameters such as purity, potency, and composition. Our team of experts employs state-of-the-art equipment and methodologies to meticulously assess each product, leaving no stone unturned in ensuring their adherence to regulatory requirements.
Our commitment to excellence extends beyond mere compliance; we strive to ensure that all analyzed products are not only safe for human consumption but also possess the efficacy and potency necessary for their intended therapeutic purposes. Through our rigorous analysis processes, we provide assurance to consumers and regulatory bodies alike, fostering trust in the integrity of herbal products in the market.
Furthermore, our efficient operations ensure timely delivery of analysis reports, with turnaround times typically within two months of submission. This promptness allows manufacturers and stakeholders to proceed with the necessary regulatory processes expeditiously, facilitating the smooth transition of products to market availability.
To facilitate accessibility and affordability, our fee structure is tailored to accommodate both local and foreign entities. We charge GHs 615 for Ghanaian companies and manufacturers, while foreign companies are assessed at $250, ensuring equitable access to our services.
In summary, the Centre for Plant Medicine Research is dedicated to upholding the highest standards of quality and safety in herbal product analysis. Our meticulous approach, coupled with timely delivery and affordability, makes us the preferred choice for herbal product registration analysis by the FDA and industry stakeholders alike.
[/vc_column_text][/vc_column][/vc_row]We subject all submitted products to three different laboratory analysis :
Microbiology
Microbial load testing evaluates product safety based on microbial contamination levels, while anti-microbial activity assesses product efficacy against microbes..
Pharmacology
We determine LD50 and safety margin by administering the product to lab animals in varying doses, observing for toxicity symptoms over 14 days, and calculating LD50 through log-dose analysis, ensuring a wide margin of safety indicates product safety.
Phytochemistry
In phytochemistry assays, we assess the product’s physical parameters such as pH, total solid residue, and color, ensuring compliance with WHO standards. Additionally, we analyze phytochemical constituents to confirm plant origin and detect potentially harmful chemicals.