Orphan Drugs – annieblogshere

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Discussion Forum, Orphan Drugs, Special Cases

Orphan Drugs

August 20, 2016 — 0 Comments

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Towards excellence in Regulatory Affairs

A pharmaceutical professional's journey to becoming an expert in Regulatory Affairs.

Achievements:

Promoted to Regulatory Affairs Associate within the organisation I work for

High Distinction in Law, Ethics and the Regulation of Medicines

Expertise & skills:

eCTD
Regulatory submissions - CAT3, SRR, SAR, MEC (injections, tablets)
CPD
GMP Clearance
Export

Interpersonal relationships
Intercultural communication
Professional and cultural sensitivity
Highly cooperative and collaborative

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