Clinquest
Linical is a leading global provider of medical affairs and pharmacovigilance services, offering comprehensive solutions for clinical safety management, postmarketing surveillance, and drug safety across various therapeutic areas. Established in 2005, Linical leverages cutting-edge systems and a team of highly trained professionals to ensure regulatory compliance, safety, and efficiency in clinical trials and postmarketing activities. The company aims to support clients in achieving successful clinical development and maintaining long-term patient safety.
Industries
Nr. of Employees
small (1-50)
Products
Our Clinical Pharmacovigilance Services
End-to-end clinical safety management including safety management plan development, database setup, medical monitoring, and ICSR processing.
Our Postmarketing Pharmacovigilance Services
Comprehensive postmarketing safety surveillance including adverse event management, literature review, and aggregate report management.
Our Clinical Pharmacovigilance Services
End-to-end clinical safety management including safety management plan development, database setup, medical monitoring, and ICSR processing.
Our Postmarketing Pharmacovigilance Services
Comprehensive postmarketing safety surveillance including adverse event management, literature review, and aggregate report management.
Services
Clinical safety monitoring, medical review and full case processing for clinical trials and postmarketing products.
Adverse event intake, literature review, social media monitoring, aggregate reporting and regulatory submissions for marketed products.
Product inquiry management, consumer and HCP call center intake, complaint documentation and coordination with PV and QA.
Setup, validation, UAT, hosting and maintenance of validated safety databases for global case processing.
Preparation and submission of periodic safety reports and expedited reports to regulatory authorities in required formats.
Clinical safety monitoring, medical review and full case processing for clinical trials and postmarketing products.
Adverse event intake, literature review, social media monitoring, aggregate reporting and regulatory submissions for marketed products.
Product inquiry management, consumer and HCP call center intake, complaint documentation and coordination with PV and QA.
Setup, validation, UAT, hosting and maintenance of validated safety databases for global case processing.
Preparation and submission of periodic safety reports and expedited reports to regulatory authorities in required formats.
Expertise Areas
- Cardiology and vascular medicine
- Dermatology
- Endocrinology
- Metabolic diseases and syndromes
Key Technologies
- Validated safety database (21 CFR Part 11 compliant)
- Artificial intelligence for pharmacovigilance
- Robotic process automation (RPA)
- Automated workflow and reporting systems
News & Updates
An article discussing key considerations in pharmacovigilance outsourcing.
An article emphasizing the significance of multicultural teams in clinical trials.
An article on the impact of AI and automation in clinical data management.
An article exploring AI's role in sales efficiency.
An article discussing ethical considerations in pediatric trials.
An article discussing key considerations in pharmacovigilance outsourcing.
An article emphasizing the significance of multicultural teams in clinical trials.
An article on the impact of AI and automation in clinical data management.
An article exploring AI's role in sales efficiency.
An article discussing ethical considerations in pediatric trials.