Life Sciences

There has been substantial growth in the volume of research in pharmaceutical and life sciences companies in recent years driven by the need for cures to life-threatening diseases and by the race to discover the next large, profitable drug or medical device. Pharmaceutical product development can take up to 15 years and $1 billion or more per product. Advances in life science research have dramatically increased the volume of documents and data as well as the size and complexity of research being conducted. Those who manage life science departments must make sure that this information is shared with key team members so that decisions can be made quickly and correctly based on pertinent information, while maintaining compliance with government regulations such as FDA's 21 CFR Part 11 as well as conforming with industry standards like GAMP4, GCP and GLP.

P-Wave recognizes compliance with the FDA's 21 CFR Part 11 is a critical issue for organizations using electronic records management systems. As a result, P-Wave has introduced solutions for the Pharmaceutical and life sciences industries that handle the volume of data and related documents in a compliant manner that conforms to industry standards. P-Wave offers solutions that are affordable and focused on ease of use and ease of integration. The key is to make enterprise class documents and data management systems readily available to everyone in a controlled and compliant web based environment.

P-Wave offers solutions in the following areas for Life Sciences:

• Environmental Laboratories
• Contract Research Organizations
• Integration with LIMS
• Integration with Laboratory Instruments
• SDMS