Fda Consulting Services From Regulatory Affairs Associates

FDA Consulting services is the fastest and most efficient way to secure product approvals with the strict FDA

. Regulatory Affairs Associates [RAA] are the experts in this field and getting licensed at an efficient and affordable pace is possible with RAA. RAA holds insider knowledge combined with over thirty-five years of experience in FDA approvals to offer you an unparalleled service, regardless of the size of your business. Founded by Lawyer/Chemist Stephen Goldner, an industry leader and former Vice President of two prominent pharmaceutical companies before starting his own companyRAA. His handpicked expert team consists of highly experienced medical IT biotechnologists, intellectual property specialists, anesthesiologists, microbiologists, scientific advisors, and toxicologists.

The purpose of this unique team is to super speed your project through the FDA drug approval process and the medical device notification procedure. They understand the difficulty of FDA preclinical tests and clinical trials. RAA works closely with you throughout the entire process. Their professional and industry knowledge backed up by Goldners team of intellectuals, RAA guarantees success through all preclinical tests. RAAs motto: Get the approval, maintain the approval, expand the approval, and restore the approval.

Regaffairs.net is simple and user-friendly, and is designed to offer the necessary contact information and in depth biographies on each individual member of Goldners team. An exact list of various drugs RAA has already worked to approve is detailed, as well as a variety of medical devices. RAA has extensively documented the entire FDA approval process for both drugs and medical devices, from GMP Compliance, to SOP Writing, Formulation, Validation and much more. RAA helps you get your project through the labyrinth of government regulations so you can focus your time and energy on other priorities.

Additionally, RAAs specialists improve your speed of medical device and pharmaceutical import approvals, while maintaining the global compliance standards of the international marketplacedrastically reducing the length of market introduction, which means rapid marketing and an immediate cash flow. RAA owns offices in Canada, US, and Europe, which means they can also assist you in devising a solid drug and medical device export strategy.

For the ease of efficiency, simplicity and cost-effectiveness in an otherwise difficult and challenging maze of FDA regulations, RAAs team of experts is the ideal solution to reduce labor and time. Whether your purpose is to approve your project, or import regulated medical technologies, RAA comes with decades of experience and extensively documented knowledge to aide your business growth as quickly as possible.

For a complete information guide to RAA and its origins, services, and staff please visit us at regaffairs.

by: Timmy Vic

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