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Sobre mim
I am a qualified dentist who transitioned into the field of Clinical Research and later specialized in Medical Writing. With over 7 years of experience in the industry, I bring a strong foundation in clinical operations and regulatory documentation.
Expertise:
1. Regulatory Medical Writing for global submissions
Development of clinical trial protocols, Clinical Study Reports (CSR), and Informed Consent Documents (ICD)
2. Preparation of eCTD module documents for regulatory authorities
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