Web
Solution for Clinical Trials Information Management Meta-Xceed Background
Since 1997, MXI (Meta-Xceed Inc.) is dedicated to creating
innovative Software Solutions and Services for companies in the clinical
research: Pharmaceutical, Biotechnology, Contract Research Organizations
and Medical Device companies. MXI specializes in Software and Services
in biostatistics, validation with compliance to CDISC and CFR
Part 11, clinical data management, medical writing, and project
management. Meta-Xceed's software tools, therefore, tremendously reduce
the time for pharmaceutical and biotech companies in preparing their
submissions to the FDA.
Understanding
Clinical Data
Meta-Xceed
has consulted to many pharmaceuticals, biotechnology and CRO
companies, contributing to its in-depth understanding of the
intricacies of clinical data. This knowledge is pivotal to the
understanding of how data is captured within a data management
system and transformed in a data warehouse before being distilled
into an electronic submission. All of Meta-Xceed's software tools
were developed from this industry experience to deliver systems that
are easy to use and optimize workflow.
Clients
Many
progressive and innovative companies, including Genentech,
Pharmacyclics, Allergan, Alza, Roche Bioscience, Quintiles, VaxGen,
and Gilead Sciences, have been Meta-Xceed's clients. They span a
diverse group of biotechnology, pharmaceuticals and Clinical
Research Organizations.
Technology Leader with Innovative Software Solutions
Specializing in the integration of the
SAS
System with Web Technology, MXI offers comprehensive tools for
optimizing the analysis, reporting, and validation of clinical data.
Products include:
Experienced and Quality Services
MXI has the combination of skilled and experienced team along with
MXI innovative Software products. We offer quality service solutions
at reduced time and cost. Recent Services include:
- Data
Standardization & Transformation to CDISC, CFR Part 11 or ISS
- Electronic
Submission Define PDF/XML documentation
- SAS System
Validation during Upgrade to 9.1.3 and SAS programs/data
verification.
- Adverse Event and
Drug Codings Solutions with Dictionaries such as MedDRA and WHO
Drug.
- Analysis and
Reporting of Clinical Trials Data.
- Custom Software
Solutions for Web Based thin client architecture or batch
environments.
1751 McCarthy
Blvd
Milpitas, CA 95035
408-955-9333
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