When it comes to product safety and quality, we pay close attention to every stage of our production process, starting from procuring top-quality raw materials from leading global suppliers of the hygiene industry and implementing strict manufacturing process controls to rigorous testing and quality inspection of finished products.
We continuously work towards designing and manufacturing products that meet and exceed not only regulatory requirements, but also our customers' expectations in terms of protection, comfort and safety. We believe you should know what exactly goes inside your period products, so we transparently disclose our ingredients and their supply chain.
Procuring top-quality raw materials
We believe that high-quality product can only be produced if we start off with safe and top-quality ingredients. Therefore, we only work with leading industry suppliers who share our core values and comply with the strictest internationally-accepted safety standards.
Before sourcing an ingredient from a supplier, we ensure that both their manufacturing control processes as well as their quality management systems are certified by independent organizations. To maintain consistency and quality of all of our raw materials, we also conduct periodic plant visits and audits to verify that our suppliers follow the same high standards and accountability that we expect from ourselves.
Implementing Strict Manufacturing Process Controls
Sparkle’s manufacturing facility has been audited by independent third-party organizations to verify that our quality management and product safety protocols meet international standards. Besides being US FDA registered, our manufacturing facility is also ISO 13485 and ISO 9001 certified.
ISO 13485 certification demonstrates that we have met all the strict regulatory requirements for our medical devices through increased transparency while maintaining high-quality standards through documentation, tracking, and feedback loops.
Implementing Strict Manufacturing Process Controls
Sparkle’s manufacturing facility has been audited by independent third-party organizations to verify that our quality management and product safety protocols meet international standards. Besides being US FDA registered, our manufacturing facility is also ISO 13485 and ISO 9001 certified.
ISO 13485 certification demonstrates that we have met all the strict regulatory requirements for our medical devices through increased transparency while maintaining high-quality standards through documentation, tracking, and feedback loops.
ISO 9001 focuses on quality and consistency. It ensures that we deliver high quality products consistently that meet all regulatory requirements.
US FDA (The US Food and Drug Administration) is an American organisation responsible for protecting public health by ensuring the safety, efficacy, and security of drugs, biological products, and medical devices. We have received their clearance as well.
We follow strict hygiene and manufacturing process control at every step of our production process. Our production area has epoxy flooring and central air conditioning with positive pressure. Our dust-free production area is equipped with an advanced Heating, Ventilation and Air Conditioning (HVAC) system that is designed to maintain a Class 10000 Clean Room environment. With hand sanitizers installed at every entry point, our dress code includes compulsory hair nets, uniforms, and safety shoes for all our technicians, engineers, and operators, so that we can deliver a clean, pristine product, in line with every hygiene requirement.
Rigorous Quality Control of Finished Products
To ensure that our products meet the highest quality standards consistently, we have implemented a rigorous internal quality management system to test every parameter - during every production run, we conduct an on-line quality inspection on the production floor as well as do a periodic sample testing of in-depth product quality analysis in our quality assurance lab.
Whether it is an on-line quality inspection or in-lab product tests, we carefully document all the performance parameters such as absorbency, rewet, and adhesive strength with individual batch codes.
Rigorous Quality Control of Finished Products
To ensure that our products meet the highest quality standards consistently, we have implemented a rigorous internal quality management system to test every parameter - during every production run, we conduct an on-line quality inspection on the production floor as well as do a periodic sample testing of in-depth product quality analysis in our quality assurance lab.
Whether it is an on-line quality inspection or in-lab product tests, we carefully document all the performance parameters such as absorbency, rewet, and adhesive strength with individual batch codes. Our standardized operating procedures allow us to effectively identify any manufacturing defects or errors so that we can quickly take corrective actions if required. That way, you can be assured that every final product that makes its way into your hands has passed every check in our rigorous quality control system, and therefore, is safe for you to use.