Looking to upgrade your EU MDR literature workflows? Let PubhHive help.

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PubHive Navigator Saas Use Cases for Literature & Safety

Goodbye workarounds. Hello workflow.

 An alternative to rigid standalone tools cobbled together with manual workarounds, PubHive Navigator is a flexible and fit-for-purpose platform that optimizes existing scientific literature and safety processes.

PubHive R&D and Medical Affairs Use Cases

Systematic Literature Review Projects

Literature Monitoring & Curation for Journal Clubs

Systematic Literature Review Projects

Systematically identifying, reviewing, and selecting literature according to explicit inclusion/exclusion criteria in order to answer a clearly formulated research question.

Living Systematic Literature Reviews

Literature Monitoring & Curation for Journal Clubs

Systematic Literature Review Projects

Continuously updating literature reviews through the active monitoring of the evidence and incorporation of relevant new evidence as it becomes available. 

Literature Monitoring & Curation for Journal Clubs

Literature Monitoring & Curation for Journal Clubs

Literature Monitoring & Curation for Journal Clubs

 Identfying and discussing the latest scholarly research articles from peer-reviewed scientific, technical, and medical (STM) journals.

Reference & Literature Management

Reference & Literature Management

Literature Monitoring & Curation for Journal Clubs

Organizing personal research libraries and automating the creation of bibliographies, footnotes, and reference sections in scholarly research papers, studies, and reports.

Managing MSL-Approved Content

Reference & Literature Management

Full-Text Journal Article Access

Organizing controlled lists of references that are approved for Medical Science Liasion (MSL) activities.

Full-Text Journal Article Access

Reference & Literature Management

Full-Text Journal Article Access

Providing users with one-stop lowest legal cost access routing to full-text papers plus integration with 3rd party document delivery supply services when individual article purchasing is required.

Document Delivery Savings

Document Delivery Savings

Document Delivery Savings

Lowering total cost of ownership (TCO) for companies that already have a document delivery service.

Get in touch to see how PubHive can support your use cases

Contact US

PubHive Regulatory, Safety & Vigilance Use Cases

Literature Surveillance for EU MDR Clinical Evaluation Reports

Literature Surveillance for EU MDR Clinical Evaluation Reports

Literature Surveillance for EU MDR Clinical Evaluation Reports

Monitoring published literature to fulfill regulatory requirements related to the identification and review of clinical data in pre-clinical evaluation, clinical evaluation, and post-market surveillance phases.

Evidence-Based Regulatory Affairs Research

Literature Surveillance for EU MDR Clinical Evaluation Reports

Literature Surveillance for EU MDR Clinical Evaluation Reports

Performing research that involves the use of scholarly literature and other types of non-literature content, across a variety of online data sources.

Pharmacovigilance (PV) Global Literature Surveillance

Literature Surveillance for EU MDR Clinical Evaluation Reports

Pharmacovigilance (PV) Global Literature Surveillance

Systematically identifying and screening literature indexed in databases such as PubMed in order to identify potential adverse events (AEs) and safety signals related to drugs, vaccines, biologics, cosmeceuticals, and other healthcare products.

Pharmacovigilance (PV) Local Literature Monitoring

Pharmacovigilance (PV) Local Literature Monitoring

Pharmacovigilance (PV) Global Literature Surveillance

Monitoring of publications that are not indexed in global databases such as PubMed in order to identify and screen literature for potential AEs and product safety signals.

Periodic Aggregate Safety Reporting

Pharmacovigilance (PV) Local Literature Monitoring

Aggregate Report Scheduling & Tracking

Performing and overseeing aggregate safety reporting functions, including report tracking, scheduling, preparation, writing, quality control, document management, audit logging, reporting, and analytics.

Aggregate Report Scheduling & Tracking

Pharmacovigilance (PV) Local Literature Monitoring

Aggregate Report Scheduling & Tracking

Auto-scheduling of aggregate safety reports plus bulk assignments of responsible report owners.

Signal Surveillance, Detection & Validation

Signal Surveillance, Detection & Validation

Signal Surveillance, Detection & Validation

One-stop monitoring and automated detection of potential safety signals with tools for streamlining follow-on assessment and documentation processes.

Signal Management & Meetings

Signal Surveillance, Detection & Validation

Signal Surveillance, Detection & Validation

Centralizing safety signal management oversight processes, meetings, and documents.

Get Started With PubHive Navigator

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