Worried about Chlamydia, Gonorrhea, Syphilis, Hepatitis B or Herpes then Test Now!

Take control of your sexual health with a discreet and reliable Chlamydia Test Kit, providing rapid results in the comfort of your own home. Our home-use Chlamydia Testing solutions empower you to screen for one of the most common sexually transmitted infections (STIs) in the United States quickly and confidentially.

Syphilis, a prevalent bacterial infection caused by Treponema pallidum, is primarily spread through sexual contact. If left untreated, this infection can progress through distinct stages, potentially leading to severe and life-altering health complications. Many individuals may be unaware they are infected, making routine Syphilis Testing absolutely essential for early detection and effective treatment. With rising rates of syphilis infection across the USA, the critical need for readily available and convenient Syphilis Test options is more pronounced than ever.

Hepatitis B is a serious liver infection caused by the Hepatitis B virus (HBV). It's one of the most common viral infections worldwide and can lead to chronic liver disease if left untreated. Many individuals with Hepatitis B may not experience symptoms, which increases the risk of unknowingly transmitting the virus to others. Our Hepatitis B Rapid Test Kit empowers you to take proactive steps toward your health by providing confidential and accurate results in the comfort of your own home, reducing the risk of unknowingly carrying the virus.

QUALITY AND ACCURACY The screening kits we supply have been chosen for their quality and reliability in STD/STI screening. We supply kits that have a high rate of agreement compared to laboratory testing using ELISA or PCR methods. ELISA or PCR testing methods are carried out in a testing laboratory and are seen as reliable and accurate methods by which to compare another testing products performance. A very high agreement rate for a rapid STD/STI screening kit indicates a similar result to a gold standard laboratory test. A low agreement rate indicates a poor performance compared to a laboratory test and should not be considered a suitable product. Agreement rates vary slightly across the various STDs due to various factors but in general products have an agreement rate of between 95%-100%. The ISO and GMP manufacturing standards also ensure consistency of production quality. Some test such as Chlamydia test for the detection of an antigen, in this case a bacteria. Other test kits such as Hep B test for antibodies produced by the human immune system in response to infection. Each STD screening method relies on its own detection window period in order to function. It is important to understand the detection window period of each test you are taking to ensure that it complies with the test kit requirements. Disclaimer: Rapid test kits are designed as a primary screening solution and all results should be consulted with your health professional. It is important to read and follow the instructions carefully.

ISO 13485 The ISO 13485 Medical Device Standard is an internationally recognized quality standard which states the requirements of the Quality Management System (QMS) for the design and manufacture of Medical Devices. Certification to ISO 13485 requires its quality system to pass a third-party Medical Device Single Audit Program, or “MDSAP” audit. ISO 13485 is recognized by WHO. You can read more about ISO 13485 here https://en.wikipedia.org/wiki/ISO_13485 What ISO 13485 means to the consumer: Consumers can purchase products carrying the ISO 13485 standard knowing that the design and manufacturing process is legally compliant and meets quality management assurance. Additionally, the manufacturing plant is inspected annually by ISO staff.

GOOD MANUFACTURING PRACTICE Good Manufacturing Practice (GMP) is a regulatory framework designed to ensure that products, particularly in the pharmaceutical, food, and cosmetic industries, are consistently produced and controlled according to strict quality standards. Unlike simple post-production testing, GMP focuses on "building quality into the process" from the very beginning. It covers every aspect of production, including the cleanliness of the facilities, the training of personnel, the quality of raw materials, and the maintenance of equipment. The primary goal is to minimize risks—such as cross-contamination, incorrect labeling, or chemical imbalances—that cannot be fully detected through testing a finished sample alone. To maintain compliance, manufacturers must adhere to what are often called the "5 P's" of GMP: people, premises, processes, procedures, and products. This requires a heavy emphasis on meticulous documentation; in the eyes of regulators, if an action was not documented, it legally never occurred. Standard Operating Procedures (SOPs) must be followed for every task, and any deviation from these rules must be investigated and recorded. By enforcing these rigorous, traceable standards, GMP ensures that consumers receive safe, effective products while protecting companies from the catastrophic legal and financial risks of product recalls or contamination.