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Supplement to October 2019ADDRESSING BARRIERS TO PATIENT CARE: Market Access Challenges With Active Therapies Nathan Stable, MD, Moderator Sean Goodall, CPA, MBA Winston Wong, PharmDDistributed withProvided
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Step 1: Collect all relevant clinical data and research studies related to the topic.
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Step 2: Review the collected data and identify any gaps in the current clinical evidence.
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Step 3: Conduct additional research or clinical trials to fill those gaps and generate new evidence.
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Step 4: Analyze the newly generated evidence and compare it with existing evidence to draw conclusions.
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Step 5: Document the findings and present them in a standardized format, such as a clinical evidence report.
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Step 6: Share the current clinical evidence with relevant stakeholders, such as healthcare professionals, regulatory authorities, and researchers.
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Step 7: Continuously update the clinical evidence as new studies or data become available.
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Step 8: Repeat the process periodically to ensure the most up-to-date and accurate clinical evidence on the topic.

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Healthcare professionals who make treatment decisions based on the latest clinical evidence.
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Researchers who seek to build upon existing knowledge and contribute to the field.
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Regulatory authorities who evaluate the safety and efficacy of medical interventions.
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Healthcare policymakers and administrators who develop guidelines and protocols.
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Medical device and pharmaceutical manufacturers who need evidence to support product development and regulatory submissions.
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Current clinical evidence refers to the most recent and relevant data from scientific studies and research related to a particular medical condition or treatment.
Healthcare providers, researchers, pharmaceutical companies, and regulatory bodies are typically required to submit current clinical evidence.
Current clinical evidence can be filled out by compiling and analyzing data from clinical trials, case studies, and other research studies.
The purpose of current clinical evidence is to support medical decision-making, treatment guidelines, and regulatory approvals.
Information such as study design, patient demographics, treatment outcomes, adverse events, and statistical analysis must be reported in current clinical evidence.
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