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Drug Safety
Under the scrutiny of bodies such as the FDA, EMA, and PMDA, continued pressure is being placed on Drug Safety to track adverse events correctly in accordance with ever-changing regulations, making it progressively more difficult to remain vigilant and effective in regard to drug safety.
IT Minds can help your company remain effective in Drug Safety, offering expertise in the Submission, Reviewing, Cleansing, and Migration of Data, whilst providing SAE Reconciliation. With a strong grounding in IDMP, Compliance Tracking, and Quality Tracking, we can help you deliver adverse events reports to the authorities with confidence.
Why Choosing Us
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Why Choosing Us
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What We Offer
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What We Offer
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Research
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Our commitment to quality assurance and compliance is second to none, and our state-of-the-art facilities are always up-to-date with the latest regulations. In addition, our team of highly trained professionals has years of experience in this field, and they are always available to answer any questions or address any concerns. Lastly, we pride ourselves on our quick turnaround times, ensuring that our clients always have the most up-to-date information.
Our Drug Safety services are designed to help you ensure the safety and efficacy of your drugs and devices. We offer a full range of Drug Safety services, from pre-clinical through post-marketing, including Drug Safety Management Plans, Clinical Trial Drug Safety Services, Drug Evaluation, and Risk Assessment, Pharmacovigilance, and Adverse Events Reporting and drug Regulatory Compliance Consulting.
In order to ensure the safety of our patients, we take a proactive approach to Drug Safety, with a number of processes and systems in place to detect and mitigate risks. We also work closely with other stakeholders, such as regulatory authorities, healthcare professionals, and patient groups, to ensure that our Drug Safety activities are aligned with their needs and expectations.
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Fatima JahraDeveloper
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