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Solutions Across the Drug Development Life Cycle Our information management services support every aspect of the drug
development lifecycle, from discovery, clinical trials, and regulatory approval to
manufacturing, marketing, and medical affairs. Drug Discovery
Streamlining drug discovery requires sound strategic planning, system design, and software implementation services for cheminformatics and bioinformatics systems. IIQ Life Sciences has in depth subject knowledge in this sector.
Designing a strong Content Management System backbone is another area where The IIQ Life Sciences can assist your organization in the Drug Discovery process. We understand that knowledge is the key and adequate security can be built into the system so that knowledge is available to the right people at the right time. The IIQ Life Sciences can provide a means for eliciting knowledge from other divisions and organizations and using this information to improve processes, procedures, etc. through a Knowledge Management Practice in the Drug Discovery process and at the same time keep intellectual capital within your own organization.
Global trials, increased volume of clinical trials, use of outsourcing partners, evolving regulatory trends, and innovative treatment combinations have made clinical information gathering and decision support more complex than ever. Each extra day of clinical development can cost millions in lost revenue and delay the introduction of vital new drug therapies for consumers. Clearly, the ability to streamline the clinical process is mission critical.
IIQ Life Sciences can assist you in implementing Electronic Record Submission process as per 21CFR Part 11 guidelines. This coupled with a robust Document Management System can ease the approval process to a great extent. Our regulatory services portfolio include audit preparedness in the areas of GMP, GLP and GCP. Our vast understanding of Global drug related regulations help our clients in preparing their drug marketing efforts globally.
To assist organizations in meeting the challenges of a constantly changing validation environment, The IIQ Life Sciences provides practical services tailored to the specific needs of clients in the pharmaceutical, medical device, biotechnology, chemical and other regulated industries. Encouraging close collaboration, our teams of consultants guide clients through GMP compliance, and validation programs that address clinical, laboratory and manufacturing systems and processes. Our clients' systems satisfy performance expectations and defined requirements in a cost-effective manner. Successful engagements have included custom-developed client systems and processes, vendor-supplied out-of-the-box solutions, and systems that were configured or customized for standalone and integrated environments.
More than 50 percent of FDA "483" notices are the result of non-compliance with document management regulations. Process changes, controlled by approved documentation, must be implemented quickly while maintaining product quality and batch integrity. At the same time, competitive pressures within the industry demand increased efficiency, shorter manufacturing cycles, and cost reductions. Implementing a controlled Document Management System typically reduces the document approval time by at least 50%.
At IIQ Life Sciences, we use the best people, processes, and technologies to manage the complex business needs of pharmaceutical sales and marketing. We understand the life sciences industry-the organizations, interactions, dependencies, influences, and transactions. We understand the marketplace-from supplier to provider, payer to patient, and all points in between. We understand technology-from the Internet and Intranets to Data Warehousing and Document Management-and how it is best applied to sales and marketing. IIQ Life Sciences can help create a Customer Relationship Management system which as a direct interface between your organization and your marketplace. An interface with regular product updates, current pricing, etc. can be created to push educational information to the right set of people.
The "e-revolution"
is profoundly changing the life sciences industry, transforming the way products are
discovered, developed, approved, distributed, prescribed, and consumed. We have expertise in addressing the needs of organizations for solutions within the enterprise for e.g. an Enterprise Information Portal (EIP) to an extended enterprise incorporating Customer Relationship Management, Catalogue Management or Supply Chain Management in order to realize the e-Business goals set by the enterprise in its vision to be the best along the value chain.
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Solutions across the Drug Development Life Cycle |
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