Digitalization and Industry 4.0 – How to Increase Productivity and Compliance in Pharmaceutical Processes

  • March 23, 2021
    1:00 pm - 3:00 pm


Ontario, Canada

Certification Areas

Course Outline
• What is Industry 4.0
• The internet of things and other concepts that bring digitalization to our personal and professional life
• The 3 basic steps to Industry 4.0. (how to start and get quick results)
• Industry 4.0 and Digitalization applied to increase results in the pharma industry (real examples).

o How digitalization is already bringing results for the pharmaceutical industry
o The need to integrate correctly (ERP, equipment, cloud, validation)


Course Objective
Digitalization, the Internet of Things and Industry 4.0 are in the spotlight right now, but what does that mean for a regulated industry? How can these concepts help us to improve pharmaceutical processes, increasing productivity at the same time that we ensure the highest standards of compliance? The objective of this webinar is to explore these questions, helping you to better understand the results that these technologies can bring to the pharmaceutical industry.
IT solutions have never been so affordable, solutions that 10 years ago would take millions of dollars and months to implement, can now be in production in a few weeks, by a fraction of the price. However, one thing will never change, new technologies only make sense if implemented in harmony with each industry’s needs and regulations, always intending to increase productivity, quality and compliance standards.


Who should attend?
This webinar applies to all personnel involved with pharmaceutical manufacturing processes. Managers, directors, process owners, system owners and users looking for ways to improve processes and to understand how industry 4.0 will positively impact GMP processes.


Course Leader: Rodrigo Correa, PMP, MBA, Lean Six Sigma Green Belt.
Having worked for companies like Siemens, Novartis and PharmEng, Rodrigo is currently the Head of Canadian Operations at Oransys, a company dedicated to increasing the pharmaceutical industry’s compliance and productivity standards.
He has been implementing IT solutions in regulated industries for the past 20 years, and is highly experienced with Warehouse Management Systems, Manufacturing Execution Systems, Performance Monitoring (OEE) and other solutions, Rodrigo also carries a strong background in Computerized Systems Validation and believes in creating value to the industry through the use of smart and cost-effective IT solutions.

Registration Deadline: 18 Mar 2021

Student Ticket: $100.00 On Sale
Basic Member Regular: $210.00 On Sale
Pro Ticket Regular: $180.00 On Sale