Lifecycle Technologies (LCT) provides a wide variety of services to help pharmaceutical companies meet International Regulatory challenges. Our team members specialize in guiding pharmaceutical companies to establish efficient, cost-effective and quality systems, which will pass inspection and produce high-quality products.
LCT consultants have varied expertise in all aspects of Quality, from writing SOPs, protocols and Master Plans needed to set up a new manufacturing facility to reviewing existing systems for compliance, effectiveness and efficiency. The pool of experts includes specialists in auditing (including extensive international experience with a practical knowledge of specific European regulatory requirements), process validation, computer validation (including 21 CFR Part 11 compliance), equipment qualification, utility and environmental monitoring, microbiology issues, and all aspects of manufacturing. We have helped our clients to achieve Operational Readiness and create Business Efficiencies while meeting their Compliance needs.
All LCT consultants come from biopharmaceutical backgrounds and have worked successfully with many traditional pharmaceutical and biotech clients. We have an unrelenting passion to deliver brilliant client service, one of the core values of our firm. We have worked with our clients to deliver high-impact results for business challenges and goals with delightful results for our clients.