Enliven: Pharmacovigilance and Drug Safety

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Journal Sections
Pharmacovigilance Signal
The relationship between drug and the adverse event to allow drug to act.
Pharmacovigilance Data Management
Generation of reliable and statistical data from pharmacovigilance studies.
Design and Development of Drug
Rational designing and developing drugs based on the biological targets.
Principles of Pharmacology
The principles to understand and predict drug effects in human body.
Quality System and Pharmacovigilance
The process of monitoring the licensed drug effects to identify and evaluate unreported adverse reactions.
Pharmacovigilance Softwares
Softwares developed to run the pharmacovigilance steps.
Drug Regulatory Activities
The process of protecting public health by controlling the safety and efficacy of pharmaceutical drugs.
Drug Reactions and Diagnosis
Study and diagnosis of drug reactions over the biological targets.
Clinical Trials and Pharmacovigilance
The research investigations in pharmacovigilance to test new treatments, interventions to prevent various diseases.
Marketing Surveillance
The process of monitoring drug after its release in the market.
Pharmacovigilance Ethics and Regulations
Basic principles and ethics in pharmacovigilance.
Biomarkers and Pharmacology
The process of using biomarkers in pharmacology to track the drug actions.
Concepts and Trends in Pharmacovigilance
Current enhancements and trends in the field of pharmacovigilance.
Drug Delivery Systems
The path, approach, and transport of drugs to reach the biological target.
Clinical Pharmacovigilance
The clinical approach to deal with drug discovery and drug delivery.
Periodic Safety Update Reports
Reports used to provide a safety update on medicinal product.
Good Pharmacovigilance Practice
The good practical approaches in pharmacovigilance set by European Union to evaluate the processes.
Pharmacovigilance Regulatory Updates
Regulatory update reports of pharmacovigilance.
Drug Safety Survillance
The process of monitoring drug through the entire drug pathway.
Pharmacovigilance for Alternative Medicine
Process to handle alternative medicine post marketing clinical trials.
Europe Pharmacovigilance
Good Pharmacovigilance Practice in European Union.
US Pharmacovigilance
Good Pharmacovigilance Practice in United States.
Japan Pharmacovigilance
Good Pharmacovigilance Practice in Japan.
UK Pharmacovigilance
Good Pharmacovigilance Practice in United Kingdom.
Pharmacovigilance Methods
Several methods included in Pharmacovigilance.
Drug Related Problems in Health Care
Adverse affects and adverse events of the pharmaceutical drugs.
Clinical Drug Manifestations of Adverse Drug Reactions
Study of adverse drug reactions.
Medical Evaluation of Adverse Events
To monitor the adverse events in the body and to evaluate the usage of medicine.
Journal Features
  • All submissions will undergo vigorous peer review process.
  • High quality review process.
  • Permanent published archives.
  • Author loyal benefits.
  • Reviewer credits.
  • Visible specified citations.
  • Open access - Maximum dissemination.
  • Un-interrupted author communication.
  • Standard author guidelines.
  • Minimal publication charges with convenient and safe modes of transfer.
Author Invitation

Enliven: Pharmacovigilance and Drug Safety is an open access peer reviewed journal. Publisher, editors’ of the journal welcomes new manuscripts. We request all authors to go through the “Author Guidelines” for any assistance regarding the authorship and manuscript submission.

Journal accepts many types of articles as discussed in “Author Guidelines”.  All received submissions will undergo vigorous single blind peer review process. Editors, reviewers of the journal have all rights to decide the quality, process criteria, and criticize the literature based upon the article content.

Journal processes all articles in a well-streamed line that includes following steps

1)    Pre quality checks to analyze the standards of the submission.
2)    Editor assignment to article research field editors.
3)    Peer review process in single blind review mode.
4)    Frequent author notifications to enhance the submission quality.
5)    Repeated peer review process to evaluate revised submission.
6)    Frequent editor notifications to keep editor engaged with submission.
7)    Author final disposition to have final acceptance from authors to proceed for further publishing steps.
8)    Post acceptance process that includes copyediting, proof reading, page making, galley corrections, HTML process, DOI assignment, and online publishing.
9)    Author Galley proof allows authors’ to modify the article with respect to alignment and any other corrections.
10)    HTML version, DOI assignment, and in-press versions will allow authors’ to check the online content.
11)    Invoice with safe and secure modes of transfers to facilitate authors to pay for the publication.

Author Benefits:
Journal provides significant benefits for authors publishing with Enliven: Pharmacovigilance and Drug safety.
1)    All articles published with the journal will undergo vigorous peer review process.
2)    Most efficient mode of article processing of the journal will allow fast publication with no quality compromise.
3)    Journal follows and supports multiple open access statements resulting in high dissemination of published submissions.
4)    Journal maintains uninterrupted communication among authors, reviewers, and editors to have rapid publication process.
5)    Journal follows specified manuscript outlines to minimize the process delay in peer review.
6)    Authors retain copyright while readers of the journal can only read, distribute, and make use of citations.

Author Loyal Benefits:
Enliven: Pharmacovigilance and Drug Safety honors the authors those who submits their multiple submissions with very reliable discounts and minimizes the publication charges.

Enliven: Pharmacovigilance and Drug Safety encourages the authors with minimum publication charges those who recommends the journal to their peers, and colleagues.


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