Instructors / Consultants

Our Main strength:

Our instructors / consultants around the world are the main strength of EASY GLOBAL TRAINING. This is the key in how uniquely we serve our clients around the globe. In short, we link you to local experts in the field of your interest with many years of industry and clinical trial experience so that they can help you with your country-specific scenarios. Therefore, this will save you time and effort to achieve your goals faster and more efficiently.

The world of regulatory compliance is moving towards a global harmonization. And we are getting closer to such harmonized compliance enforcement. However, we have still a long way to reach that point. This is exactly where EASY GLOBAL TRAINING, with a global network of instructors / consultants, can help to bridge this gap.

Our Experts:

All of our online regulatory and quality training / consulting are conducted by these experts with several years of industry experience in their field of expertise.

We have experts in the following areas to help take the burden off your shoulders so you have time to focus on more important areas:

  • Clinical trials
  • IND fillings
  • NDA filings
  • Variations and amendment filings
  • Manufacturing authorization
  • Compliance
  • Quality control / QC
  • Clinical trial set-up
  • Marketing authorization (drugs & devices)
  • Audits
  • Regulatory body communications
  • Briefing documents (FDA / EMA / ROW)
  • Response letters (FDA / EMA / ROW)
  • Good Practices  / GXP

Our online regulatory training / consulting in the following areas:

  • Regulatory guidelines (FDA. EMA, China, Japan, Australia, …)
  • Manufacturing authorization
  • Quality control / QC
  • Worldwide approval process
  • Global standards / USP
  • Marketing authorization process (drugs & devices)
  • Audits
  • Labeling / Packaging requirements

Good practices / GXP is another area we focus on and have modules covering the following:

  • Good clinical practice / GCP
    • Good clinical laboratory practice / GCLP
  • Good manufacturing practice / GMP / cGMP
    • Good automated manufacturing practice / GAMP
  • Good laboratory practice / GLP
    • Good automated laboratory practice / GALP
  • Rest of GXP course:
  • Good auditing practice / GAP
    • Good auditing practice / GAP
    • Good clinical data management practice  / GCDMP
    • Good cell culture practice / GCCP
    • Good distribution practice / GDP
    • Good documentation practice / GDocP
    • Good publication Practice / GPP
    • Good guidance practice / GGP
    • Good microbiological practice / GMiP
    • Good pharmacovigilance practice / GVP / GPvP
    • Good pharmacy practice / GPP
    • Good research practice / GRP
    • Good safety practice /GSP
    • Good storage practice /GSP

Our training pieces are available in different formats by our instructors / consultants (drugs / devices / Excipients / Food & Food ingredients / Dietary supplements):

  • Webinars
  • eLearning courses
  • In-class courses
  • E-books
  • Job aids
  • Templates
  • On-site training

Please feel free to browse our collaborator’s site (Neometrix Consulting Inc.).

Please follow us on YouTube, Facebook, LinkedIn, Twitter, Instagram, Pinterest, and Tumblr, to get updates of what is new.

We are always looking for instructors / consultants to collaborate with to enrich our online training / consulting for services to accommodate more areas of expertise

If you are willing to join us as an instructor / consultant, fill out the following form. we will then get in touch with you. Please note that the mandatory fields are marked with an asterisk.




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