Compliance & Ethics
We adhere to the highest standards of Good Manufacturing Practices (GMP) to ensure the safety, quality, and efficacy of our products. Our commitment to good manufacturing processes involves rigorous quality control measures, state-of-the-art facilities, and continuous staff training. We follow stringent good manufacturing standards to prevent contamination, mix-ups, and errors, ensuring that every product meets global regulatory requirements.
WHO Good manufacturing practice (GMP) is a system for ensuring that products are consistently produced and controlled according to quality standards. it is designed to minimize the risks involved in any pharmaceutical production that cannot be eliminated through testing the final product . The main risk are : unexpected contamination of health or even death., incorrect labels on containers, which could mean that patients receive the wrong medicine ., insufficient or too much active ingredient, resulting ineffective treatment or adverse effects.
WHO GMP covers all aspects of production: from the starting materials, premises and equipment to the training and personal hygiene of staff. Detailed, written procedures are essential for each process that could affect the quality of the finished product. There must be systems to provide documented proof that correct procedures are consistently followed at each step in the manufacturing process – every time a product is made.
WHO has established detailed guidelines for good manufacturing practice. Many countries have formulated their own requirements for GMP based on WHO GMP.
ISO Standards contribute to making the development, manufacturing and supply of products and services more efficient, safer and cleaner. They make trade between countries easier and fairer. They provide governments with a technical base for health, safety and environmental legislation. They aid in transferring technology to developing countries.ISO standards also serve to safeguard consumers and users in general, of products.