Professional Training Suite is a one-stop solution for paperless training requirement in pharmaceutical, biopharmaceutical, healthcare and medical device industry compliant with 21 CFR Part 11 and GAMP5 guidelines
maxiQ is an integrated complete quality solution designed to improve quality at every level and therefore helps in building or developing a quality product with market standards and 21 CFR Part 11 and GAMP5 Compliant
docuDrive is an electronic document library which manages your documents entirely or to handle the document approval life cycle in a single repository in a secured environment with permission levels
easyTD is a 21 CFR Part 11 and GAMP5 compliant integrated solution for submitting the content electronically into specific modules, sections, and documents via the use of an XML (extensible markup language) backbone
Fransha Pharma LLP is a global regulatory and technical service provider for the pharmaceutical, biopharmaceutical, healthcare and medical device industry. Our goal is finding the best solution for our clients.
Fransha Pharma LLP offers specialized consultants an opportunity to work either on an individual basis or in a project-team. For dedicated projects, we support the complete life-cycle of the process. To guarantee this, we rely on our internal quality system.
Fransha Pharma LLP develops software solutions for the pharmaceuticals industry, which can digitize your end to end process with maximum quality and minimum efforts.
