По Вашему запросу ничего не найдено.
Рекомендуем сделать следующее:
- Проверьте правильность написания ключевых слов.
- Используйте синонимы введенных Вами ключевых слов, например “приложение” вместо “программное обеспечение”.
- Попробуйте воспользоваться одним из популярных поисковых запросов ниже.
- Начните новый поиск.
Pharmacovigilance
Safety teams are under enormous pressure to control ever-increasing caseloads, new sources of signal detection data, and changing regulations—all with flat budgets and resources. What if you could alleviate this pressure, while improving efficiency and strengthening compliance?
Collaborate with industry peers to advance safety.
How our customers experience Oracle for pharmacovigilance
CSL Behring trusts Oracle Argus—respected by global regulatory authorities—for safety case management
For over two decades Syneos has relied on Oracle for safety case management
4C Pharma Solutions enjoys better, more concise safety case processing without errors
PharSafer depends on Oracle Argus Cloud to process, analyze, and report adverse event cases
Ensure compliance from clinical trials through post-marketing surveillance
Automate your safety case processing
Reduce processing time by 50% while improving accuracy and compliance through AI-powered digital case intake.
Explore Safety Case IntakeMake faster, better safety decisions
Relieve the pressure of growing caseloads while maintaining compliance with global regulations and standards by automating safety case management.
Explore Argus—Safety Case ManagementConfidently detect, analyze, and manage safety signals
Automate safety-signal detection with proven algorithms developed by world-class statisticians and data scientists.
Explore Empirica—Safety Signal Management
“When you have Argus, you know you can handle everything from small Phase I to large Phase III and IV trials.”
Timo Toivonen
Vice President, Services, Crown CRO
Are you prepared for regional, post-market medical device safety regulations?
Una Kessi, Oracle Product Management, Safety and PharmacovigilanceMedical device safety reporting requirements vary by region—make sure you are up to date on the regulations and are prepared to comply.
Read the complete postFind resources and more
Is AI the key to speed and efficiency in pharmacovigilance?
In an effort to bolster pharmacovigilance programs, pharma companies have succeeded in gathering massive amounts of data—so much so that they have found themselves struggling under the weight of it, particularly around adverse event reports. Is AI the solution?
Addressing the data challenges of pharmacovigilance
Hear how pharmacovigilance managers are addressing the increase in volume and variety of incoming drug safety data.
Collaborate with industry peers to advance safety
Discuss best practices in pharmacovigilance, hear about harmonized approaches to meeting new regulatory requirements, and stay current with the Oracle safety product strategy and roadmap.
Get started with Oracle Life Sciences
Subscribe to our blog
Get the latest insights and best practices to drive your clinical success.
Get technical support
Explore technical support contacts and resources.
Follow our podcast
Hear from thought leaders on trends in life sciences.
Contact us
Contact us about clinical research and pharmacovigilance.