Life Sciences Suite
STRUGGLING WITH MULTIPLE SILOED TOOLS?
Replace your outdated legacy tools - no upgrade headaches, guaranteed backward compatibility!
ACHIEVE SUSTAINABLE COMPLIANCE
Reduce the risk and overall cost of global regulatory compliance.
ENSURE PRODUCT QUALITY, SAFETY AND EFFICACY
Scale down overall product lifecycle management efforts, get your products to market faster.
One vendor – the market leader in Medicinal Product information. The only next-generation solution available that is Integral by Design, Modular by Implementation. One authoritative source of truth.
Leverage AMPLEXOR Life Sciences Suite to manage enterprise regulated content and processes as well as publishing. Achieve and maintain global regulatory compliance.
- Best Total Cost of Ownership (TCO)
- Extremely configurable and agile in adapting to new business processes
- Ready to be validated and deployed without expensive customization
- Supports efficient enterprise-wide collaboration
- Bolsters data standardization – no data redundancy
- Ensures simple upgrades and backwards compatibility configuration
- Guarantees easy and flexible migrations, interfaces, and process automation
- Incorporates best-practice modules as a quick start
- Best design for on- or off-premises – no need for interfaces between subsystems
- Completely self-reliant as it is independent of application, tenancy, infrastructure, and location
This second-generation, compliance-centric solution suite enables life sciences companies to replace siloed tools with a single authoritative software product to proactively manage information, business processes, regulated documents, and electronic records, and to use advanced reporting tools across the entire product lifecycle: from product nomination to post-submission and post-approval maintenance. Enter or import the data into the system only once. Don’t leave your metadata redundant – leverage it over the entire product value chain!
AMPLEXOR Life Sciences Suite is built on unique and innovative Integral by Design, Modular by ImplementationTM architecture, which allows for seamless integration of all of its modules. Depending on your organization’s needs, it can support either singular compliance-relevant processes or complete enterprise compliance management. This unprecedented level of integration increases the level of efficiency, promotes enterprise-wide standardization and enables the transformation of your business. This results in lower complexity, higher overall quality of products, and sustainable compliance.
Take advantage of the best TCO on market.
QUALITY AND MANUFACTURING PROCESS
AND DOCUMENT MANAGEMENT
R&D PROJECT AND DOCUMENT MANAGEMENT (INCLUDING TRIAL MANAGEMENT)
REGULATORY DOSSIER AND SUBMISSION MANAGEMENT (INCLUDING PUBLISHING)
MATERIOVIGILANCE AND PHARMACOVIGILANCE MANAGEMENT
PRODUCT AND REGULATORY INFORMATION MANAGEMENT
ACTIONABLE BUSINESS INTELLIGENCE
The AMPLEXOR Life Sciences Suite helps users effectively tackle industry-specific challenges in R&D, Clinical Trials, RA, PhV, QA/QC, Manufacturing, etc.
AMPLEXOR Life Sciences Suite is available either as a license or as a subscription, so you can choose the option best suited to you.
Join our client circle: we pursue a partnership approach with clients.
Contact our experts
What our customers say
"MEDICE chose Your Company as its preferred provider primarily because of the integral nature of your solution. Having all information managed within one system is extremely important for us...”
Dr Stephan Rudolph, Manager Drug Regulatory Affairs, MEDICE
What our customers say
"SubmissionExpert is one of the three most important business applications used by PLIVA today."
Aleksandar Raić, Head of Integration and Strategic Project Management, Teva Pharmaceuticals