Medical Device 2020 - Tips for setting up a Quality System to withstand FDA Audits for Medical Device and Pharmaceutical Companies

In the current environment of global standardization of quality and regulatory needs, learning to understand and interpret the FDA regulatory requirements for medical device
To fulfill the ever growing, complex quality and regulatory requirements to manufacture, register and launch your medical device or pharmaceutical product in a timely manner by setting up a good quality System.
Will review FDA expectations based on her personal experience in setting up Quality Systems ( QS) in Pharma and device companies
Will incorporate several examples based on the FDA Requirements for setting up quality systems so you can integrate them into your company SOPs
Speaker:
Meena Chettiar, has worked as a Scientist for Health Canada and as a Quality Management Professional in food, pharmaceutical and medical device industries