Vimal Sachdeva, World Health Organization (WHO), CH - Qepler Summits And Conferences

Vimal Sachdeva

Technical Officer (Expert Inspector)
World Health Organization (WHO), CH
Switzerland
WHO's primary role is to direct international health within the United Nations' system and to lead partners in global health responses.

Mr Sachdeva holds a Master Degree in Chemistry as well as a Specialized Diplomas in Pharmaceutical and Biopharmaceutical manufacturing. He also holds a Postgraduate Diploma in Business Administration.

He has more than 30 years of experience including 15 years as a regulator of health products. He started his career as a chemist and moved on to lead Quality Control, Quality Assurance, Regulatory Affairs and Compliance departments within generic and innovator pharmaceutical companies. Before joining WHO, he worked with the Singapore Health Sciences Authority (HSA) as a Senior GMP Auditor and Senior Regulatory Specialist.

To date, he has performed more than 300 on-site GMP inspections (active pharmaceutical ingredients, finished pharmaceutical ingredients, vaccines and in-vitro diagnostic manufacturers) as a Lead Inspector in Asia, Africa, Latin America and North America.

Related Sessions:

2nd Annual Genotoxic Impurities in
Pharmaceuticals Summit 2021

Genotoxic Impurities in Pharmaceuticals strategies & new methodologies: analysis, in silico & regulations. Challenges & opportunities.
  • 15 Jul 2021
  • Virtual,
  • Pharma
Day 1: Thursday, 15 July 2021
CASE STUDY: Regulatory Updates on Nitrosamine Impurities.

It has become mandatory to understand current regulations and recommendations by FDA, EMA, WHO and other authorities to implement adequate quality risk management principles to make science-based decisions to mitigate potential risks. Competent staff, sound knowledge and in-depth understanding of products and processes are critical when assessing potential risks to manufacturing processes to ensure that patient safety is adequately protected.

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