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Posted 4 days ago by CK Group- Science, Clinical and Technical
Plan and track activities related to regulatory submissions in the EU. Systematic communicator of regulatory submission dates, regulatory status, nature of changes, track and inform of minor/significant product information changes to all relevant parties. Provide logistic support for … more
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Posted 15/10/2024 by CK Group- Science, Clinical and Technical
Supports the team with regional regulatory strategies in line with business plan for post-approval activities. Supports the team to complete identified regulatory activities to ensure all regulatory obligations and business objectives are met. Prepares and compiles regulatory submissions ( … more
