Toxicology Literature Reviews and Post-Market Surveillance
Turn complex scientific literature into clear, defensible decisions. ScitoVation provides toxicology literature reviews, chemical risk assessment support, and post-market surveillance for organizations that need reliable evidence for product safety, regulatory submissions, and ongoing risk management.
Built for: pharmaceutical, biotechnology, chemical, consumer-product, product-stewardship, regulatory, and safety teams.
Find the Evidence That Matters
A literature review should do more than collect publications. It should answer a defined scientific or regulatory question through a transparent, reproducible process.
Our scientists define the question, identify and screen relevant studies, evaluate quality, extract critical findings, and organize the evidence into a focused assessment your team can use.
Clear findings, not an information dump
Understand what the available science supports, where uncertainty remains, and which action should follow.
Scientific Review and Ongoing Surveillance
Toxicology Literature Review Services
Focused evidence review for chemical safety, biological effects, exposure, and potential human-health risks.
- Search strategy and review protocol development
- Systematic and targeted literature searches
- Study screening, selection, and data extraction
- Study-quality and toxicological endpoint evaluation
- Weight-of-evidence analysis
- Evidence-gap identification
- Chemical and product safety assessment
- Regulatory-ready toxicology reports
Post-Market and Pharmacovigilance Surveillance
Structured monitoring to identify emerging findings and evaluate potential safety signals after market entry.
- Pharmacovigilance signal detection support
- Adverse event literature monitoring
- Phase 4 post-marketing surveillance
- Product and ingredient safety monitoring
- Emerging-risk identification
- Periodic literature updates
- Evidence review and signal assessment
- Documentation for internal and regulatory review
From Search Strategy to Actionable Findings
Define the Question
Clarify the product, chemical, endpoint, population, exposure, and decision the review must support.
Build the Protocol
Establish databases, search terms, screening criteria, quality standards, and documentation needs.
Evaluate Evidence
Screen literature, extract data, assess study quality, and identify patterns, limitations, and gaps.
Synthesize Findings
Organize the evidence into a clear narrative, weight-of-evidence assessment, or surveillance report.
Support the Decision
Deliver findings scientific, regulatory, legal, and product teams can use to determine next steps.
Scientific Depth Without Unnecessary Complexity
ScitoVation combines toxicology expertise, structured literature-review methods, and practical regulatory understanding. The work is scientifically credible, clearly documented, and directly relevant to the decision your organization needs to make.
- A review designed around a defined scientific question
- Transparent and reproducible methods
- Experienced toxicology and risk-assessment support
- Clear documentation of sources, criteria, and conclusions
- Flexible support for one-time reviews or ongoing surveillance
- Findings that communicate across scientific and business teams
Discuss Your Review or Surveillance Need
Tell us about the product, compound, safety question, or monitoring requirement. A ScitoVation scientist will follow up to understand the decision, evidence, and timeline.
Submission does not create a consulting relationship or guarantee project acceptance.