MakroCare’s division MakroCare Consulting, a high-end consulting service provider, offering regulatory, risk management and consulting services to life sciences companies across the globe, is organising an interactive Webinar on Best practices for Computer System Validation in compliance with 21 CFR Part 11 on September 24 from 4 pm to 5 pm.

This is the first time any company is attempting to assist bioPharma & pharmaceutical companies in addressing the challenges posed in “Conceptualizing and Implementing a Computer System Validation programme and its compliance to 21 CFR Part 11”.

Nitesh Shrivastava, Regulatory and CSV consulting to US FDA regulated Industries, Udaya Kumar Chandrashekhar, a practicing consultant in healthcare, IT and distribution domains and Tinoy Abraham, a consultant in the FDA-regulated industries of pharmaceuticals, medical devices, clinical trials, and drug development specializing in computer system validation will be the speaker to answer the Q’s of the Webinar participants.

The Webinar is expected to attract IT managers, project managers, compliance managers, regulatory managers, QA and drug safety professionals in medical/healthcare/ pharmaceutical/biotech industries.

For registration, log on: www.makrocare.com and register or contact +91 040- 44346622 for any queries.