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Author: MarksMan Healthcare

    Marksman Healthcare > Articles by: MarksMan Healthcare

25Oct

Is There Any Dogma Regarding Informed Consent in the Conduct of Pragmatic Trials?

by MarksMan Healthcare,  0 Comments

Clinical trials are instrumental for health science community to test and evaluate interventions. Trials can be broadly categorized in two classes, i.e. pragmatic and explanatory; where the former are designed […]

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17Oct

Whats is the Reality and Future of Real World Evidence?

by MarksMan Healthcare,  0 Comments

The term real-world evidence (RWE) commonly applies to data generated in non-randomized clinical trials (RCTs) in a healthcare setting, which sometimes also covers patient socio-economic data and environmental data. Irrespective […]

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21Sep

How to Elicit Expert Opinion to Understand Missing Health Outcomes?

by MarksMan Healthcare,  0 Comments

Missing data are a big concern in any research project and are often unavoidable in spite of investigators’ best efforts. Missing outcomes have two effects: reduced precision and power, and […]

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14Sep

How Strong is the Evidence for Drugs Receiving FDA Accelerated Approval?

by MarksMan Healthcare,  0 Comments

A recently published study by Dyer O (2017) exposed major drawbacks in the accelerated approval process of some drugs available to the American patients without any stringent clinical evidence of […]

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06Sep

How Data Visualization is Helping in Healthcare Decision Making?

by MarksMan Healthcare,  1 Comment

Health informatics systems are evolving with an aim to revolutionize health and healthcare programs worldwide. However, turning this hope-filled vision into a reality will take enormous effort from thousands of […]

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26Aug

Excerpts from the Workshop – “R WE Ready?” – “Real World Evidence” Methods!

by MarksMan Healthcare,  0 Comments

Workshop title – “R WE Ready?” – “Real World Evidence” Methods! Organisers – Co-organised by Organisation of Pharmaceutical Producers of India (OPPI) and ISPOR India-Mumbai Chapter Objectives – To enhance skill […]

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21Aug

How the Future of Clinical Trials in India Looks Like?

by MarksMan Healthcare,  1 Comment

According to the data from clinicaltrials.gov, 1.4% of global clinical trials are done in India, when the country has 16% of the world’s population and carries 20% disease burden in […]

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11Aug

How Important is to take Ethics Approval for Survey Research?

by MarksMan Healthcare,  0 Comments

Ethics are the moral principles that distinguish between right and wrong. In research, they differentiate between acceptable and unacceptable behaviours on the part of the researcher. Ethical considerations in research […]

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10Jul

Scoping Reviews: An Evolving Concept in EBM

by MarksMan Healthcare,  0 Comments

Scoping reviews are exploratory projects that systematically map the literature on a topic, identifying key concepts, theories and sources of evidence. Scoping reviews are often conducted before full syntheses, and […]

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  • J1309, Amethyst Tower, PBEL City, Peeramcheruvu, Rajendra Nagar Mandal, Hyderabad, Telangana – 500091
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Using Synthetic Controls in Oncology Real-World Data Studies for Treatment Insights

September 20, 2023

Strategizing Optimal Collection and Use of Real-World Data from Expanded Access Programs

September 18, 2023

International Reference Pricing vs. Value-Based Pricing: Drug Pricing Strategies

September 11, 2023

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  • J1309, Amethyst Tower, PBEL City, Peeramcheruvu, Rajendra Nagar Mandal, Hyderabad, Telangana – 500091
  • Call Us: +91-9160467576
  • enquiry@marksmanhealthcare.com

Latest Blogs

Using Synthetic Controls in Oncology Real-World Data Studies for Treatment Insights

September 20, 2023

Strategizing Optimal Collection and Use of Real-World Data from Expanded Access Programs

September 18, 2023

International Reference Pricing vs. Value-Based Pricing: Drug Pricing Strategies

September 11, 2023

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