eQMS Software Provider greenlight.guru Inks Partnership with MedTech Regulatory Compliance Consulting Firm Pearl Pathways
INDIANAPOLIS, IN (PRWEB) November 09, 2015 -- greenlight.guru, a leading eQMS software provider to the medical device industry, announced today its newly formed partnership with Pearl Pathways, a comprehensive life science regulatory compliance consulting services company.
This strategic alliance will have a direct impact on the medical device community by helping foster better collaboration and adoption of product development best practices for early to mid-stage medical device companies. By pairing greenlight.guru’s award winning quality management software with the industry knowledge and expertise of Pearl Pathways, customers are able to better navigate regulatory hurdles, shorten time to market, reduce risk and improve patient outcomes.
greenlight.guru officially announced its partner program during the spring of 2015 and has already established key relationships across the globe. David DeRam, CEO & co-founder of greenlight.guru shared, “The regulatory landscape is changing and global regulatory bodies are becoming more risk-centric. Companies are adopting new technologies to navigate these hurdles. Working with partners like Pearl Pathways allows us to get our customers out in front of those changes.”
Some of the most innovative medical device companies in the world use greenlight.guru’s eQMS solution. Unlike other legacy systems, greenlight.guru’s eQMS software solution was designed to be easy to use, allowing customers to begin receiving value within the first few hours of use, helping ensure compliance and reduce risk from idea stage through product commercialization.
Acting as an extension to a customer’s internal team, Pearl Pathways helps guide and support functions spanning process optimization to regulatory strategy and filings. With deep expertise in regulatory, quality compliance, clinical, and product development, Pearl Pathways focuses on accelerating product development. “Our dedication to driving improved value and efficiency in product development is one of our core values. Partnering with greenlight.guru amplifies this position and further assists our customers in accelerating their regulatory pathway to success,” stated Diana Caldwell, CEO and President of Pearl Pathways.
About Pearl Pathways
Pearl Pathways accelerates life science product development acting as an extension of their clients’ teams by partnering with clinical teams, in-house regulatory experts, quality compliance specialists, quality auditors, and senior leadership teams to get life saving devices, diagnostics and therapeutics to market sooner. Pearl Pathways’ talented employees are focused on completing critical research, ensuring high quality and efficient manufacturing of products, accelerating global product registrations, and keeping clients up to date on current regulatory and quality compliance trends and best practices for life science product development. Pearl Pathways is located in Indianapolis, Indiana, is AAHRPP accredited, and a WBENC certified woman owned business. Visit http://www.pearlpathways.com, call 317-899-9341, or e-mail contact(at)pearlpathways(dot)com to connect with a subject matter expert.
About greenlight.guru
greenlight.guru produces beautifully simple software solutions for medical device companies to allow them to bring high quality products to market faster, while reducing risk and simplifying regulatory compliance. greenlight.guru’s QMS software solution provides device makers a Single Source of Truth by integrating the management of design controls, risk, controlled documents, and quality processes in one, easy to use platform. To learn more about how greenlight.guru’s quality management software solution can help your team get its product to market faster, visit http://www.greenlight.guru or call 317-762-5311 to schedule your free personal demo today.
Nick Tippmann, greenlight.guru, http://greenlight.guru, +1 (260) 438-8708, [email protected]
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