Techy Pharma LLP
ID: #1285707
Listed In : Software Development
Business Description
Techy Pharma LLP is a technology company specializing in advanced software solutions for pharmaceutical, biotechnology, CRO, and life sciences organizations. The company develops intelligent digital platforms that help businesses manage regulatory compliance, clinical trials, training management, quality processes, and laboratory operations efficiently.
Techy Pharma provides AI-powered solutions such as Clinical Trial Management System (CTMS), Electronic Training Management System (ETMS), Smart Electronic Trial Master File (eTMF), Cognitive Quality Management System (QMS), Electronic Case Report Form (eCRF), Document Management System (DMS), Laboratory Information Management System (LIMS), and 21 CFR Part 11 compliant Electronic Signature software. These solutions help organizations streamline workflows, maintain audit readiness, and ensure compliance with global standards including FDA 21 CFR Part 11, GxP, and other pharmaceutical regulations.
The company focuses on helping pharmaceutical companies, contract research organizations (CROs), biotech firms, and research institutions digitize operations, improve productivity, and maintain regulatory compliance across the entire product lifecycle. Techy Pharma delivers secure, scalable, and cloud-based software platforms that support modern pharmaceutical research and regulatory processes.
Learn more about our solutions at:
https://techypharma.com/
Business Hours
Monday : 09:00 - 18:00
Tuesday : 09:00 - 18:00
Wednesday : 09:00 - 18:00
Thursday : 09:00 - 18:00
Friday : 09:00 - 18:00
Saturday : 09:00 - 18:00
Sunday - Closed
Techy Pharma LLP
Techy Pharma LLP provides innovative software solutions designed specifically for the pharmaceutical and life sciences industry. Their platforms such as Clinical Trial Management System (CTMS), Electronic Training Management System (ETMS), and Quality Management System (QMS) help organizations streamline regulatory compliance and clinical trial operations. The team demonstrates strong technical expertise and a clear understanding of global pharmaceutical regulations such as FDA 21 CFR Part 11 and GxP. Their solutions are reliable, scalable, and well suited for pharmaceutical companies, CROs, and research organizations looking to digitize their compliance and research workflows.