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Regulatory Affairs for Medical Devices

I'm helping companies to authorize and launch products globally, in the following key areas: Registration process for Cosmetics, Medical Devices, OTC, IVD and Food to FDA approval process, INVIMA (Colombia), COFEPRIS (Mexico), Peru, Panama.. The regulatory process from product design to market entry for a new medical device, IVD or Cosmetic is oftentimes complicated and unclear. It can also become difficult to make a clear distinction between your regulatory strategy and Registration process.

Our consulting services can help your product company develop an intelligent, effective strategy to obtain efficiently product registration approval and access the markets in the United States and other countries for Latin-America

As a freelancer, I am undertaking most frequently transcription, document formatting, copy typing, proofreading, rewriting and editing projects.

I am honest, reliable, hardworking, highly organised, methodical, conscientious, professional and friendly.
If you require any further information please do contact me.

Skills & Expertise

AccessCertificate ManagementClient ContactConsultantCopy & PasteCosmeticsCosmetics IndustryDesignFood LawGlobal HealthInternational Affairs IndustryLatin TranslationMedicalMedical Device DesignRegulatory OperationsStrategy

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