FDA Registration Certification

What is FDA Registration Certification?

FDA Registration is a widely adopted and standardized Quality Management System (QMS) for the Aerospace industry. The aerospace community has specific requirements that need to be taken into account, and the QMS needs to incorporate these critical requirements. The FDA Registration Certification was introduced in 1997 by the International Aerospace Quality Group (IAQG) based on the internationally recognized standard ISO 9001 in order to encourage International quality, safety, and technology standards in air transport. The certification can be applied to all areas in aviation like design and manufacture of equipment, airport and airline operations, aircraft accessory supply, spares supply, and maintenance.

FDA Registration shows compliance with the United States Food and Drug Administration (FDA or USFDA) which is a federal agency of the Department of Health and Human Services. The FDA is responsible for protecting and promoting public health through the control and supervision of food safety, tobacco products, dietary supplements, prescription, over-the-counter pharmaceutical medications, vaccines, biopharmaceuticals, blood transfusions, medical devices, Electromagnetic Radiation Emitting Devices (ERED), cosmetics, animal foods & feed and veterinary products being sold or manufactured in the United States. The FDA regulates more than US$2.4 trillion worth of consumer goods, about 25% of consumer expenditures in the United States. The FDA also inspects and enforces regulations related to these industries.

Why do I need Kwikcert in particular?

Because we keep the entire process simpler, FDA Registration Certification can take just 7 – 30 days to complete the process based on your company’s size. In fact, our ‘Hassle-free certification’ approach provides the following benefits

• Reduce the time taken to acquire ISO 9001 Certification
• No Certification cost
• We provide you access to web-based online Process Repository Software to manage your complete process documentation
• 24/7 access to our back end support team who can manage your process documentation remotely
• Reduce management time required
• Reduce the cost of maintaining Certification

Benefits of FDA Registration

Applying the FDA Registration will help administrations to work with an OH&S management system that can advance its occupational wellbeing and security management in the following ways.

• Developing and executing a rigorous and comprehensive OH&S policy along with objectives
• Establishing smart operational controls for managing OH&S risks along with its legal ramifications and other factors
• Clearly marking the jeopardies and perils associated with OH&S and its activities and then trying to eliminate them; it may also involve the implementation of controls which can reduce their potential effects
• Founding actual systematic courses that consider the opportunities and risks as well as the legal aspects of FDA Registration
• Evaluating the overall OH&S performance as well as coming up with ways to improve it by taking various types of suitable arrangements
• Increasing the awareness of OH&S risks
• Making sure that the workers and employees actively follow all OH&S matters

Implementing theFDA Registration can also help to make sure that a company gains a strong reputation as a safe and healthy place to work. This can also encourage new potential employees to get interested in working with the company. It can also have the following benefits:

• It can help in enhancing the ability of a company to attend all regulatory compliance issues
• It can bring down the cost associated with the insurance premiums
• The standard can reduce the costs associated with downtime as well as disruption of operations
• It can make it easier to reduce the costs of all incidents
• It can also minimize absenteeism in a major way and also enhance employee turnover rates

It can bring recognition that comes with achieving an international benchmark. This can also impact the mindset of the customers who may become positively concerned about their diverse safety and social responsibilities.

Who should follow FDA Registration?

FDA registration is the basic requirement for domestic and foreign establishments that manufacture or market food, drug, API, or medical devices in the USA. The FDA exercises authority for inspections of facilities in foreign countries which supply pharmacy and food products to the US. FDA Registration gives access to key markets in the US. It assures clients that their service requirements will be fulfilled. There is an improvement in process reliability through FDA Registration. It offers competitive differentiation by demonstrating reliability and high quality of service.

FDA is one of the many services offered by KwikCert, the global consulting and certification solutions provider. FDA Registration applies to any company size and any industry wanting to operate in the USA. We deliver FDA consulting and certification services across the globe.