EAM, CMMS, CCMS Solution
Your ultimate goal is to introduce a new, safe, effective therapy to market. Achieving that goal involves sophisticated processes and products that must meet the highest of standards.
If you are an early-stage R&D company, you might have complex analytical instrumentation. If you are a firm engaged in Phase III clinical trials or full production, everything you do and produce is subject to GMP standards. In either case, you want your labs, processes and facilities to be cost effective, efficient and compliant.
Since 1992, Blue Mountain has been offering the solutions you need for managing your assets and achieving compliance across the board. Our Blue Mountain Regulatory Asset Manager software and support represent the industry standard for calibration, maintenance and validation. Flexible and highly configurable, Blue Mountain RAM was designed to serve your specific industry. It enables biotech companies of every size and stage to put Best Practices in place and helps you coordinate and automate your work at a price even the youngest start-ups can handle.
Blue Mountain Quality Resources:
- Offers Deep Biotech Domain expertise
- Develops functionalities specific to the biotech industry
- Offers specific solutions for small, medium and large-sized firms
- Integrates calibration and maintenance management
- Enables GMP compliance for Part 11, Part 58, Part 211 and Part 606
- Has biotech experience at Amgen, Biogen, Genentech, Wyeth and hundreds of others
Blue Mountain will take you from Project Assessment to System Implementation to On-Going Support. Read more about Blue Mountain RAM and our suite of services.
