Aims and Scope

B R Nahata Smriti Sansthan International Journal of Pharmaceutical Sciences and Clinical Research (IJPSCR) is quarterly international journal, being published in the months of March, June, September and December by BRNSS Publication Hub, Mandsaur. It is an academic, online, open access, peer reviewed international journal. The aim of the journal is to:

  1. Disseminate original, scientific, theoretical or applied research in the field of Pharmaceutical Sciences and Clinical Research.
  2. Dispense a platform for publishing results and research with a strong empirical component.
  3. Aqueduct the significant gap between research and practice by promoting the publication of original, novel, industry-relevant research.
  4. Seek original and unpublished research papers based on theoretical or experimental works for the publication globally.
  5. Impart a platform for publishing results and research with a strong empirical component.
  6. Create a bridge for significant gap between research and practice by promoting the publication of original, novel, industry-relevant research.
  7. Solicit original and unpublished research papers, based on theoretical or experimental works.

B R Nahata Smriti Sansthan International Journal of Pharmaceutical Sciences and Clinical Research (IJPSCR) covers topic of all Pharmaceutical Sciences and Clinical Research branches. The main topic includes but not limited to:

Pharmaceutical Sciences

  1. Pharmaceutics,
  2. Novel drug delivery and targeting systems,
  3. Medicinal and pharmaceutical chemistry,
  4. Pharmaceutical and biological analysis,
  5. Pharmcokinetics,
  6. Pharmacodynamics,
  7. Pharmacology,
  8. Pharmacognosy,
  9. Pharmacotherapy and clinical pharmacy,
  10. Pharmacy practice,
  11. Pharmacoeconomics,
  12. Pharmacoepidemiology,
  13. Analytical biochemistry

Clinical Research

  1. Clinical trial methodology,
  2. Traditional results papers,
  3. Clinical trial design,
  4. Conduct,
  5. Decision analysis,
  6. Synthesis,
  7. History,
  8. Statistical methods,
  9. Data management,
  10. Legal, ethical and regulatory issues,
  11. Case record form design,
  12. Data collection,
  13. Quality assurance,
  14. Data auditing methodologies,
  15. Risk-benefit,
  16. Cost-effectiveness,
  17. Clinical or policy impact of all types of clinical trials and related medical research methodologies.