by Prakash Achaary | Jan 25, 2023 | Blog
Regulatory Information Management Systems Software (RIMS) are centralized platforms designed to support and streamline Regulatory Affairs teams and operations. RIMS helps in the creation, organization, submission, and archival of regulatory information in regulated...
by Prakash Achaary | Jan 17, 2023 | Exclusive
A. Expanded Access for Treatment Use Q1. What is expanded access? Q2. Are there safeguards in place for expanded access use of an unapproved drug? B. Expanded Access Submission Q3. What types of regulatory submissions can be used to obtain expanded access to a drug...
by Prakash Achaary | Jan 16, 2023 | Blog
In this blog, we sat down with Daria Fellrath, Senior Manager of Global Talent and Culture Management at MMS, to discuss how important it is to align a global team, engage with colleagues, and foster human connections across organizations. Daria’s leadership and...
by Prakash Achaary | Jan 11, 2023 | News
BANGALORE, India (1/12/2023) – MMS Holdings, a data-focused contract research organization (CRO), has been named a Great Place to Work by the Great Place to Work Institute of India. This award is based on anonymous feedback from a survey sent out to employees and...
by Prakash Achaary | Jan 4, 2023 | Blog
The Clinical Trials Information System (CTIS) is a single portal for European Union (EU) competent authority and ethics submissions for clinical trial applications (CTAs) across EU member states. The system represents the actualization of the EU Clinical Trials...