Oracle
Clinical
L S Technologies (LST) is proud
to offer “Software
as a Service” or (SaaS) clinical software for Biotech,
Pharmaceutical, Therapeutic and Medical Device firms, as
well as Educational Institutions that need a robust technology,
but do not want to be saddled with the burden of costly
hardware, software and manpower requirements to manage
the day to day operational functionality of the systems.
LST can help your organization,
achieve, and sustain a competitive advantage through
the deployment of these world-class software technology
offerings. Our team of seasoned
professionals will architect and deploy your business specific,
R&D, Clinical, Adverse Effect, Trial & Site Minder
Application solutions using the latest FDA Certified methods,
providing cost effective solutions in the shortest possible
timeframe. Deployment can be in as little as one
week. The system is 21 CFR PART 11 compliant and
is delivered and accessed over the Internet through 128
Bit Encryption, thus assuring priority data security. Other
highlights include:
- US FDA: Title 21 CFR Part 11, Electronic Records and
Electronic Signature
- US FDA: Guidance for Industry for Computerized Systems
Used in Clinical Trials
- US FDA: Title 21 CFR Best Clinical Practices
- International Conference on Harmonization (ICH)
- Clinical Data Interchange Standards Consortium (CDISC)
and Health Level 7 (HL7)
- 24/7 data management on a global basis
- Help to facilitate and manage
collaboration between internal groups and external
partners while ensuring each group is able to access
only the information you have previously authorized
- Help to accomplish the goal of
moving from “paper” to
EDC (Electronic Data Capture)
Additionally, we provide your Certified
S.O.A’s
with each implementation.
Our steadfast commitment to client satisfaction is evident
in every interaction. Our expert staff will assist you
through every phase of solution acquisition and deployment.
As for the pricing model, we understand
the financial challenges facing businesses today. That
is why we have based pricing of the product on a per
user basis. Whether your company has 1 or 100 employees,
you only pay for the services you use.
So ask yourself; “Why you
would want to spend hundreds of thousands of dollars
in start up and management costs to track your Clinical
and Adverse Effect needs, when you can get it at a fraction
of the cost and have the expertise of LST available to
you?”
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