| Healthcare |
| Our innovative technical solutions
help Biotech and Pharmaceutical companies reduce time
and cost in all phases from therapy discovery,
development through sales and marketing. We also help
healthcare companies integrate silos of information to become more proactive, responsive and
regulatory compliant. |
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 Drug Discovery |
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Early identification of successful active compounds for more focused development, determining concrete causes of diseases from genomic data and optimizing the time to market for new drugs have significant effects beyond Research and Development. For the Life Sciences Companies it means higher sales with lower investments.
We provide solutions that help integrate data from various disparate internal and external sources that leverage industry standard data formats, make it easier to glean meaningful information from a deluge of data and greatly enhance collaboration among Researchers. Our solutions have the ultimate goal of reducing time and cost of drug discovery through rapid integration of information. |
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| Preclinical-Clinical |
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Increased volumes of trials in various phases of development, evolving regulatory trends and the inherent complexity of information gathering pose tremendous challenges.
Therefore our solutions built on secure, web-based platforms offer easy scalability. It also provides streamlined management of Preclinical and Clinical information
that ultimately accelerates introduction of vital new drug therapies in the market and enhances your competitive advantage. |
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| Regulatory |
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Government intervention in the form of regulation is a major factor in healthcare industry. Important legislation such as Balanced Budget Amendment of 1997, Health Insurance Portability and Accountability Act of 1996 (HIPAA) pose significant technical challenges for healthcare related organizations. Discoverture offers HIPAA-compliant, web-based, secure electronic data exchange solutions to healthcare organizations handling patient data. United States Food and Drug Administration (FDA) 21 CFR Part 11 of 1997 provide governing guidelines for electronic records, signatures and submissions.
Our validated “21 CFR Part 11” ready solutions help you meet the regulatory requirements regarding electronic record keeping and e-signatures. Our solutions for management of content facilitate electronic submission of documents and records for compliance with FDA regulations. |
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| Validation |
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Discoverture builds solutions that are GxP compliant for customers in the Pharmaceutical and Biotechnology industry. Our quality processes conform to the Code of Federal Regulations and the GxP
(GLP, GCP and GMP) guidelines and adequately address the following areas:
- Data Integrity
- System Reliability
- Management Control
- Auditable Quality
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| Sales and Marketing |
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Different divisions of the Sales & Marketing department of a Pharmaceutical company subscribe to syndicated data from various vendors for tactical and strategic decision making. Most of the time numerous localized point solutions exist for acquiring the data and then delivering to internal subscribing applications after QA/QC. Unfortunately this results in high cost of maintenance, lack of consistent application of business rules for establishing data quality and standardization.
We provide highly scalable metadata driven solutions, which enable creation of a single point for all syndicated data acquisition and timely delivery to the internal users.
Please click here to review our case study for further discussion on this.
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Discoverture Solutions
Discoverture Solutions
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