VIMTA is a leading contract research and testing organisation headquartered in India, serving the pharmaceutical, food, and general manufacturing sectors. With over 40 years of experience and a global presence, VIMTA is at the forefront of supporting pharmaceutical companies with their outsourced product development and discovery activities.
Committed to advancing quality and GMP best practices among their clients, VIMTA’s leadership is dedicated to excellence. In line with our mission, SeerPharma is proud to partner with VIMTA to host a 1-Day Workshop on Computer System Validation, scheduled for Tuesday, September 10th, at Vimta Labs in Hyderabad.
The workshop will be inaugurated by Dr. A. Ramkishan, Deputy Drug Controller from India’s CDSCO, Hyderabad Zonal Office. Drawing on SeerPharma’s 35+ years of industry experience, the session will be led by Director Ian Lucas and will cover the following key topics:
- Common terms and definitions of Computerised Systems Validation
- Types and elements of System Development Life Cycles (SDLC)
- Good Automated Manufacturing Practices (GAMP)
- Critical considerations for data integrity from a GxP regulatory perspective
- Regulation of computerised systems in PIC/S (e.g., MHRA, TGA, etc.) and FDA environments
- Implementing a CSA approach through practical examples
- Recognising the compliance, risk, and regulatory implications of using computerised systems
Registration Details
Fee: INR 18,000 + GST (18%)
VIMTA Contact: Srihari Vuta
Email: Sriharireddy.vuta@vimta.com
Phone: +91 8019 216 214
SeerPharma and VIMTA are committed to continuing their collaboration in delivering Quality/GMP training workshops in India in the near future. We look forward to your support at our inaugural session in September.
