PharmaceuticalsThe Pharmaceutical industry is highly regulated with an extreme focus on product research and development. Development of new drugs can take up to fifteen years, with hundreds of people creating enormous amounts of data—each piece as important as the next. Sharing key information across project teams and making decisions based on all relevant information is imperative. Also, compliance with specific legislation, including the FDA GCP, GLP, GMP and CFR 21 Part 11 guidelines is mandatory, adding even more importance to proper information management.
TOWER Software helps Pharmaceutical companies manage and secure their vital information assets, regardless of format or medium. A secure, scalable, fast, powerful and cost-effective solution, our TRIM Context solution enables pharmaceutical companies to:
- Create, deploy, integrate and manage large amounts of data quickly, efficiently and cost-effectively
- Facilitate R&D collaboration
- Improve the flow of marketing and communications to consumer and physician buyers
- Reduce time-to-market for new drugs
- Increase operation workflow efficiency
- Maintain compliance with regulatory requirements
More specifically, with TRIM Context, pharmaceutical companies may:
- Minimise research repetition and error
- Facilitate secure access to R&D data, both internally and externally
- Allow real-time feedback from both physicians and consumer customers
- Enhance partnerships with research affiliates
- Automate personal contact processes between physicians and reps
- Co-ordinate sales and marketing activity
- Feel secure, knowing their document and records management solution is used as part of CFR 21 Part 11 environments
To be contacted with more information regarding TOWER Software’s solutions for the Pharmaceutical industry, click here.
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