QbD Approach at the Research and Development Stage itself involving due diligence particularly (but not limited to) with respect to Risk Assessment and Mitigation ensures time and cost saving processes...
Objective: Fostering a CAPA culture within the organization at all levels across various functions Enhancing Investigation process effectiveness Developing individual capability for methodological problem solving Who Will Benefit QA/ QC.
This Two – Days event will provide a basic, but a comprehensive overview of Overall Global Pharmaceutical Regulatory-Affairs in a relaxed and interactive environment, yet complete focus on Quality, Safety
Global Regulatory Agencies & cGMP compliance, always expect that complaints, failures and deviations are handled in a systematic & timely manner. In this process, the impact on the “Product Quality”.
Over the course of the last decade, we have witnessed the emergence of therapeutic antibodies, and more specifically, monoclonal antibodies (mAbs) as one of the fastest-growing classes of pharmaceutical drugs.
This course has been updated to include the update on 21 CFR Part 11 and also electronic version of CFR part 11. Further we are ensuring to make you understand...
This Two-Day online training is specifically designed to understand the travails of accommodating off-site Pharmaceutical activities including audits & Inspections With physical workplaces shut down following the Covid-19 disaster
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