Regulatory Affairs
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PHARMACEUTICALS
Regulatory Affairs
Common Technical Document (CTD)
A single dossier format reshaped global drug approvals, slashing delays and costs
7 days ago
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How did the Common Technical Document (CTD) impact the pharmaceutical drug approval process globally?
It introduced completely different requirements for each region, increasing the complexity of submissions.
It standardized the submission format, reducing duplication and accelerating approvals across multiple regions.
It eliminated the need for clinical study reports in drug approval dossiers.
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GOVERNMENT AND LAW
Regulatory Affairs
Regulatory Approval Process
How streamlined regulatory approval processes can accelerate national interest projects
21 Jan 2026
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What is the primary purpose of regulatory approval processes in government projects?
To provide unlimited funding for all proposed projects
To ensure projects comply with legal, environmental, and safety standards before proceeding
To allow projects to bypass environmental assessments for faster completion
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