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Mexico
Able to expedite the documents required by Latin America BoH. Knowledge of the different sections (CTD) that have direct impact on the product. Knowledge of Latin America regulations relative to pharmaceutical and nutritional products. Capable of preparing documents for registration, variations and product renewals.. Knowledge of Good Documentation Practices. Able to expedite legal documents that make up a dossier. Evaluation and approval of marketing material, change controls and quality complains.
Clinical Regulatory Affairs
About Me
Industry: |
Science & Biotech |
|---|---|
Occupation: |
Clinical Regulatory Affairs |
Education level: |
Bachelor |
Will Relocate: |
Yes |
