The main responsibility of all government drug regulatory agencies across the globe is to ensure that all products made available to its citizens conform to acceptable standards of quality, safety, and efficacy. Ryan supports these regulations and assists various governments with the process, on behalf of our customers, in order to meet the health demands of their population.
 
Ryan has registered hundreds of our pharmaceuticals and healthcare products worldwide. Our highly experienced registration department deals with all matters relating to the registration of our products. Our customers rely on our experience and competent staff to complete product registration effectively and efficiently. We stick by our customers, whether registration takes months or even years, until the product(s) are approved and importation of our products can be initiated.
 
Being a highly detail oriented process, product registration procedures and requirements vary according to country. However, our focus on the implementation of the most efficient registration processes has allowed us to expedite the amount of time it normally takes from submitting the registration application to product distribution. Whether it be one of our latest anti-malarial treatments, diagnostic test kits, or surgical gloves, we will see the process through to the end.

Inspection and licensing of pharmaceutical manufacturing facilities on the basis of compliance with GMP are a vital element of drug control. Ruili supports WHO initiatives aimed at improving inspection techniques and increasing the frequency of inspections for the common good of society. Besides the internal and third-party inspections we frequently conduct for quality assurance purposes, we routinely host government inspectors from abroad to gain their approval when preparing to enter new markets. 

Government inspectors represent the enforcement arm of a national drug regulatory authority. Its function is to ensure adherence by manufacturers to all licensing provisions and specifically to GMP. The objectives are to provide authorization for the importation of the manufacturer's products into the country of the inspectors. The first objective involves a sequential examination of production and control activities on the basis of GMP guidelines issued by the WHO or of nationally determined requirements. The second requires verification that production and quality control procedures employed in the manufacture of specific products are performed correctly and that they accord with data supplied in the relevant licensing applications. Inspection is also dependant on other factors such as the national legislation and regulations of the inspector's country and/or resources available. 

While the inspection criteria and procedures vary from country to country, their results do not. Ruili products have successfully been approved by health ministries and agencies from Australia to Africa, the Middle East to Asia. We realize that the future of our company depends on our continued product improvement and market expansion. Facility inspections are a top priority for us and their results reflect our policy of constant improvement and meticulous attention to detail.

Proper documentation is essential in almost every aspect of the pharmaceutical industry. Whether for product registration, factory inspection, or internal quality control, Ruili employs the latest technologies to streamline and process information. All facilities possess up-to-date Good Manufacturing Practice (GMP), CE, TUV, and/or ISO certificates that reflect high quality standards and WHO rules and regulations. Essential product registration documents, such as the Certificate of Pharmaceutical Product (COPP), Free Sales Certificate (FSC), Certificate of Origin (COO), and Marketing Authorizations are among the many documents our registration department frequently submit for registration purposes. Likewise, technical files are repeatedly checked for consistency and accuracy for both internal quality control purposes and in preparation of inspections. 
Ryan is highly specialized in the export process and has vast experience with documentation for product registration. Our customers realize the value in registering our products - the value of quality, time, and reliability.