Zurich, Switzerland: +41 - 43 434 80 33   |   US: (510) 962-8903   |   support@traininng.com

Michael Ramcharan

QA professional, QA Consultant

Michael Ramcharan has over 25 years of experience in Quality Assurance having worked with multinational Pharmaceutical and Clinical Research Organisations since 1990. His auditing experience has involved conducting a wide variety of audits in GPVP, GCP and GCLP, globally. He has also hosted and supported various Regulatory Authority Inspections (eg; MHRA, EMA, Local EU) in the GCP and GPV space. Michael’s audit experience has also extended to successfully designing, implementing, and conducting Remote audits in the GPVP arena which has allowed companies to maintain strong oversight of their Local Operating Companies and Business Partners in countries where travel restrictions do not allow for on-site audit visits.

Michael has also assisted companies in managing their Pharmacovigilance QA audit programs adopting a risk-based approach to help identify and prioritise audits. Michael has also been involved in the Training and Mentoring of auditors, providing bespoke training catered specifically to an individual’s development needs, and his varied experience has proved very valuable in this area.



  •  Friday, August 17, 2019
  • 12:00 PM CEST,
  • 60 Minutes
  • ¤115.00
ICH E6 (R2) Implementation in Clinical Operations - A Case Study

The Webinar will provide useful information on implementing policies and procedures in compliance with the applicable regulation.

  •  Friday, August 31, 2019
  • 12:00 PM CEST,
  • 60 Minutes
  • ¤115.00
QA & Pharmacovigilance Oversight of Market Research (MR) Studies

The Webinar will provide an understanding about the types of MR studies, how these can be managed to ensure that adequate safety information can be collected to assure the benefit/risk of the concerned products under investigation and the role of QA in this process.





  • Recorded
  • View Anytime
  • ¤155.00
Remote Auditing in Pharmacovigilance (PV)

The presentation will provide an insight and guidance to managers with PV QA departments to implement a Remote Auditing program, and will focus on:

  • Recorded
  • View Anytime
  • ¤155.00
ICH E6 (R2) Implementation in Clinical Operations - A Case Study

The Webinar will provide useful information on implementing policies and procedures in compliance with the applicable regulation.

  • Recorded
  • View Anytime
  • ¤155.00
Remote Auditing in Pharmacovigilance (PV)

The presentation will provide an insight and guidance to managers with PV QA departments to implement a Remote Auditing program, and will focus on:

  • Recorded
  • View Anytime
  • ¤155.00
QA & Pharmacovigilance Oversight of Market Research (MR) Studies

The Webinar will provide an understanding about the types of MR studies, how these can be managed to ensure that adequate safety information can be collected to assure the benefit/risk of the concerned products under investigation and the role of QA in this process.

300018sem
Michael Ramcharan
Date: 23 & 24 August, 2019   |   Time: 10:00 AM To 05:00 PM CEST

Management of Vendors Providing Pharmacovigilance and Clinical Trial Services to the Pharmaceutical Industry

This Seminar will provide information key to managing a successful partnership with Vendors who provide essential services in ensuring that patient safety and data integrity are of an acceptable quality and comply with applicable GCP and GVP regulations.

Price: ¤999.00