Symbiance
Symbiance is a technology‑enabled contract research organization (CRO) founded in 1990 that provides outsourced clinical development services to pharmaceutical, biotechnology and medical device companies. Services described on the site include clinical data management, data standardization using CDISC standards, biostatistics and statistical programming, and pharmacovigilance. The company states use of machine learning and predictive analytics to support clinical data solutions and offers global delivery with a US headquarters in Princeton, NJ.
Industries
Nr. of Employees
medium (51-250)
Symbiance
500 College Rd E Suite 415, Princeton, NJ 08540, United States
Patents
Products
Clinical Data Management
Provides services for collecting, recording, processing, analyzing, and reporting clinical trial data, ensuring data quality and safety, and maintaining audit trails and data storage.
Biostatistics
Offers statistical analysis and SAS programming for all phases of drug development, including protocol review, sample size estimation, and data integration.
SAS Programming
Provides SAS programming solutions for data displays, program development, validation, and documentation, ensuring compatibility with internal standards.
Pharmacovigilance
Manages drug safety and risk, including adverse event case management, aggregate reporting, signal detection, and risk management plans.
Clinical Data Standardization
Helps companies apply CDISC standards for data collection and regulatory submission, including SDTM mapping and ADaM programming.
Clinical Data Management
Provides services for collecting, recording, processing, analyzing, and reporting clinical trial data, ensuring data quality and safety, and maintaining audit trails and data storage.
Biostatistics
Offers statistical analysis and SAS programming for all phases of drug development, including protocol review, sample size estimation, and data integration.
SAS Programming
Provides SAS programming solutions for data displays, program development, validation, and documentation, ensuring compatibility with internal standards.
Pharmacovigilance
Manages drug safety and risk, including adverse event case management, aggregate reporting, signal detection, and risk management plans.
Clinical Data Standardization
Helps companies apply CDISC standards for data collection and regulatory submission, including SDTM mapping and ADaM programming.
Services
Integrated clinical data management services covering EDC support, database build, edit checks, query management, medical coding and safety reconciliation for clinical studies.
CDISC implementation services including SDTM and ADaM mapping/conversion, CRF annotation, define.xml and reviewer guide creation, and legacy data conversion.
Statistical consulting and analysis services including protocol review, sample size estimation, SAP development, interim analyses and integrated clinical/statistical reporting.
Statistical programming services for TLF generation, SAS program development and validation, ADaM specification and macro development following good clinical programming practices.
Global drug safety services including ICSR processing, aggregate reporting, signal detection, risk management planning and literature searches, with digital PV automation initiatives.
Integrated clinical data management services covering EDC support, database build, edit checks, query management, medical coding and safety reconciliation for clinical studies.
CDISC implementation services including SDTM and ADaM mapping/conversion, CRF annotation, define.xml and reviewer guide creation, and legacy data conversion.
Statistical consulting and analysis services including protocol review, sample size estimation, SAP development, interim analyses and integrated clinical/statistical reporting.
Statistical programming services for TLF generation, SAS program development and validation, ADaM specification and macro development following good clinical programming practices.
Global drug safety services including ICSR processing, aggregate reporting, signal detection, risk management planning and literature searches, with digital PV automation initiatives.
Expertise Areas
- Clinical data management
- Clinical data standards and CDISC implementation
- Biostatistics and statistical programming
- Pharmacovigilance and drug safety
Key Technologies
- CDISC SDTM
- ADaM and analysis dataset generation
- Electronic Data Capture (EDC) platforms and UAT
- SAS statistical programming
News & Updates
Announcement that a company expert (Divya Kannaiah) will speak at the ISCR Conference on the impact of new technologies on biostatisticians and statistical programmers.
Announcement that a company expert (Divya Kannaiah) will speak at the ISCR Conference on the impact of new technologies on biostatisticians and statistical programmers.