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PhaseIVProvisional Merit list of candidate Fit for Further Evaluation Processor ExpertDigital Medias. No. Name1Ashish Kumar Saurabh17103115Shamik Biswas171069822345VIVEK Misapplication Category Gender Number17106422PANKAJ
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Who needs phase-iv?

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Phase IV is typically needed by individuals or organizations involved in post-marketing surveillance of pharmaceutical products.
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This includes regulatory agencies, pharmaceutical companies, medical professionals, and researchers.
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Phase IV studies aim to assess the long-term safety and efficacy of a drug after it has been approved and made available to the general population.
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Through Phase IV studies, potential adverse effects and drug interactions can be monitored, helping to ensure the continued safety and effectiveness of the medication.
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Phase-IV refers to the fourth phase of a project or clinical trial, typically focusing on post-market surveillance and monitoring.
Entities conducting clinical trials or post-market surveillance studies are required to file phase-IV.
Phase-IV forms can typically be filled out online through a regulatory agency's designated portal or platform.
The purpose of phase-IV is to monitor the safety and effectiveness of a product in real-world settings after it has been approved for use.
Information reported on phase-IV may include adverse events, patient outcomes, and any new safety concerns.
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