RADEX Institute is a Regulatory Affairs Consultation office that helps pharmaceutical companies to classify their medical products as a drug, biologic, medical device, dietary supplement, or cosmetic.
RADEX Institute will accelerate the regulatory process to allow these products to enter the global market in a short period of time.
RADEX Institute, through its experienced team in the global regulations of drugs, medical devices, cosmetics, combination products, and dietary supplements offers a variety of training courses.
RADEX institute team is highly qualified to provide further consultation, prepare submissions, registration and solve product-related registration challenges.
Covering all types of submissions at USFDA, Europe, & MENA region, RADEX Institute offers professional and complete services in the preparation and registration of:
RADEX Institute supports pharmaceutical companies to build and maintain a strong PV system.
RADEX Institute provides Pharmacovigilance services by establishing a PSMF/ PSSF system, PV software, and onsite PV training.
RADEX Institute offers a professional RA training certificate.
This professional program will provide integrated knowledge and broad perspectives about all the regulations and regulatory processes in the USA, Europe, and MENA regions.
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