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    Academic Journals

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• A review of medical device regulations in India, comparison with European Union and way-ahead.

  Authors:Manas Manu and Gaurav AnandFrom:Perspectives in Clinical Research (Vol. 13, Issue 1) Peer-Reviewed

  Jan-March 20223,276 words Article 1820LByline: Manas. Manu, Gaurav. Anand Indian healthcare sector is a fast-growing industry which is expected to reach $280 billion by 2025. Medical devices market in India is one of the top 20 medical device markets in the...

• The critical appraisal of randomized controlled trials published in an Indian journal to assess the quality of reporting: A retrospective, cross-sectional study.

  Authors:Sandeep Gupta, Ravi Tiwari, and Raj GoelFrom:Perspectives in Clinical Research (Vol. 13, Issue 1) Peer-Reviewed

  Jan-March 20222,574 words Report 1530LByline: Sandeep. Gupta, Ravi. Tiwari, Raj. Goel Background: Although randomized controlled trials (RCTs) are the highest levels of evidence, they might not necessarily be of good quality. Hence, RCTs should always be...

• Virtual ethics committee meeting during the COVID-associated lockdown - Madras Diabetes Research Foundation Experience.

  Authors:Subramani Poongothai, Ramasamy Aarthy, Mokkapati Lalasa, Kannikan Viswanathan, and Viswanathan MohanFrom:Perspectives in Clinical Research (Vol. 13, Issue 1) Peer-Reviewed

  Jan-March 2022805 words Article 1680LByline: Subramani. Poongothai, Ramasamy. Aarthy, Mokkapati. Lalasa, Kannikan. Viswanathan, Viswanathan. Mohan Introduction The ethics committee (EC) has a vital role in an efficient review of biomedical and health...

• Identifying barriers to report adverse drug reactions using the Delphi method: Experience from an institute of national importance of India.

  Authors:Bikash Meher and Rashmi MohantyFrom:Perspectives in Clinical Research (Vol. 13, Issue 1) Peer-Reviewed

  Jan-March 20221,253 words Article 1980LByline: Bikash. Meher, Rashmi. Mohanty Background: Spontaneous reporting of suspected adverse drug reaction (ADR) is an essential component of pharmacovigilance program, however, under reporting is a major drawback of...

• Knowledge, attitudes, and perception of 398 cancer patients toward participation in clinical trials: A single-center study from New Delhi, India.

  Authors:Vishal Biswkarma, Nitesh Rohatgi, Rajesh Saxena, and S. GuptaFrom:Perspectives in Clinical Research (Vol. 13, Issue 1) Peer-Reviewed

  Jan-March 20223,372 words Article 1760LByline: Vishal. Biswkarma, Nitesh. Rohatgi, Rajesh. Saxena, S. Gupta Background and Objective: Clinical trials are considered to be the gold standard research methodology for evaluating the efficacy and safety of...

• Observational designs for real-world evidence studies.

  Author:Santosh TaurFrom:Perspectives in Clinical Research (Vol. 13, Issue 1) Peer-Reviewed

  Jan-March 20221,904 words Article 1800LByline: Santosh. Taur In the era of evidence-based medicine, real-world evidence (RWE) studies have opened avenues to utilize real-world data (RWD) effectively for improving clinical decision-making. However, the...

• A study to monitor errors in use of inhalation devices in patients of mild-to-moderate bronchial asthma in a tertiary care hospital in Eastern India.

  Authors:Neha Akhoon and D. S. BrashierFrom:Perspectives in Clinical Research (Vol. 13, Issue 1) Peer-Reviewed

  Jan-March 20223,396 words Report 1680LByline: Neha. Akhoon, D. S. Brashier Context: Bronchial asthma is a chronic respiratory disorder which affects over 300 million people worldwide. Inhalation pharmacotherapy is the cornerstone in treatment of asthma,...

• Drug use evaluation of cephalosporins in a tertiary care hospital.

  Authors:Yashashri Shetty, P. Manjesh, Widhi Churiwala, Sakshi Jain, and Vishal SinghFrom:Perspectives in Clinical Research (Vol. 13, Issue 1) Peer-Reviewed

  Jan-March 20223,081 words Article 1400LByline: Yashashri. Shetty, P. Manjesh, Widhi. Churiwala, Sakshi. Jain, Vishal. Singh Background: Infectious disease burden in India is among the largest in the world. Cephalosporins are being used extensively in the...

• The medical science liaison role in Spain: A nationwide survey.

  Authors:VíCtor Sastre, Adela Matesanz-Marín, Cristina García, and Antonio GonzáLez Del CastilloFrom:Perspectives in Clinical Research (Vol. 13, Issue 1) Peer-Reviewed

  Jan-March 20223,115 words Survey 1610LByline: Víctor. Sastre, Adela. Matesanz-Marín, Cristina. García, Antonio. González del Castillo Context and Aims: The Medical Science Liaison's (MSL's) value to the company has evolved into a more strategic role with a...

• A retrospective cross-sectional descriptive study to critically appraise the quality of reporting of health economic evaluations conducted in the Indian setting.

  Authors:Sandeep Gupta, Ravi Tiwari, and Raj GoelFrom:Perspectives in Clinical Research (Vol. 13, Issue 1) Peer-Reviewed

  Jan-March 20224,098 words Report 1680LByline: Sandeep. Gupta, Ravi. Tiwari, Raj. Goel Background: The reporting quality of economic research could benefit from enhanced quality assurance procedures. At present, there are small numbers of health economic...

• Non-inferiority trials.

  Authors:Priya Ranganathan, C. Pramesh, and Rakesh AggarwalFrom:Perspectives in Clinical Research (Vol. 13, Issue 1) Peer-Reviewed

  Jan-March 20222,166 words Article 1550LByline: Priya. Ranganathan, C. Pramesh, Rakesh. Aggarwal Studies sometimes aim to show that a new intervention is not substantially worse than the existing standard of care while offering some benefits, for example,...

• Clinical trials and Consolidated Standards of Reporting Trials: Continuing concerns of compliance in COVID-19 era.

  Author:Arun BhattFrom:Perspectives in Clinical Research (Vol. 13, Issue 1) Peer-Reviewed

  Jan-March 20221,157 words Editorial 1600LByline: Arun. Bhatt COVID-19 global pandemic's serious health consequences created an urgent unmet medical need to discover effective therapies for managing disease and preventing complications. This has led to an...