SERVICES
Regulatory Affairs
Regulatory Affairs
Comprehensive regulatory support throughout the entire product lifecycle.
Pharmacovigilance
Research & Development
Medical Writing
Medical Writing
Professional preparation of regulatory and pharmacovigilance documentation.
Medical Devices
Medical Devices
Professional support in certification and lifecycle management of medical devices.
Clinical Trials
AREAS OF EXPERTISE
We support your journey from product development to market entry with expert regulatory guidance.
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Pharmaceuticals
Research & Development
Expert consultation
Lifecycle management
eCTD submissions
Gap analysis
Regulatory affairs
Pharmacovigilance
Expert consultation
Lifecycle management
eCTD submissions
Gap analysis
Regulatory affairs
Pharmacovigilance
Medical Devices
Food supplements
Foods for special medical purposes
Cosmetics
Radaydrug
RADAYDRUG is a trusted consulting company with over 25 years of expertise in pharmaceutical and healthcare industries. Established with the vision of supporting developers, manufacturers, and distributors of pharmaceuticals, medical devices, food supplements, and cosmetics, our company provides comprehensive solutions throughout the entire product lifecycle.
Our highly skilled team combines deep industry knowledge with a strong commitment to excellence. Over the years, this dedication has positioned RADAYDRUG as a key player in the sector.
SERVICES
Radaydrug
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COUNTRIES
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CLIENTS
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PRODUCTS DEVELOPED
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PRODUCTS IN PHARMACOVIGILANCE
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PRODUCTS IN LIFECYCLE MANAGEMENT
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REGULATORY SUBMISSIONS
Since 2006, RADAYDRUG has operated a quality management system certified under ISO 9001.
This certification ensures that RADAYDRUG services are reliable and meet the highest industry standards and regulatory requirements. It is a guarantee that the Clients consistently receive precise, well-documented, and high-quality support.
