Organizer Profile
GlobalCompliancePanel

GlobalCompliancePanel

Fremont, California, United States of America

GlobalCompliancePanel is a training source that delivers diverse, high quality regulatory & compliance trainings. These trainings are simple while being relevant and cost-effective while being convenient.

GlobalCompliancePanel imparts knowledge of best practices across a broad range of user-friendly mediums such as webinars, seminars, conferences and tailored, individualized consulting. These help organizations and professionals implement compliance programs that meet regulatory demands and put business processes in place.

GlobalCompliancePanel focuses primarily on providing extensive and quality training in these core areas and anything related to them:

1. Risk Management
2. Regulatory Compliances
3. Corporate Governance
4.Quality Management

Through the mediums by which we offer trainings, namely webinars, seminars, conferences and consulting, we bring together the regulators or experts on regulation on the one hand, with the community that needs to learn or be aware of those regulations, on the other.

Professionals who undergo trainings from GlobalCompliancePanel exhibit a vastly improved quality of life in which there is increased productivity and professional growth. Some 30,000 professionals have gained from more than 500 training courses we have conducted till now.
CONFERENCES AND COURSES
FDA Scrutiny of Promotion and Advertising Practices (Jun, 2019)
  • In-Person Event-0 In-Person Event
  • Speciality Health Informatics, Medical Education ...
  • Calendar Jun 27 - 28, 2019
  • FDA Scrutiny of Promotion and Advertising Practices (Jun, 2019) in Baltimore,  Maryland, USA Baltimore, Maryland, USA
Applied Statistics for FDA Process Validation (Apr, 2019)
  • In-Person Event-1 In-Person Event
  • Speciality Healthcare Management, Healthcare Technology
  • Calendar Apr 25 - 26, 2019
  • Applied Statistics for FDA Process Validation (Apr, 2019) in Boston,  Massachusetts, USA Boston, Massachusetts, USA
CE Mark Certification: Compile a CE Marking Technical File (or Design Dossier for Class III) containing evidence of compliance to the Medical Devices Directive (or the IVD/AIMD Directives) - Impact of the MDR for Europe
  • In-Person Event-2 In-Person Event
  • Speciality Risk Management and Medical Negligence, Quality Management ...
  • Calendar Nov 29 - 30, 2018
  • CE Mark Certification: Compile a CE Marking Technical File (or Design Dossier for Class III) containing evidence of compliance to the Medical Devices Directive (or the IVD/AIMD Directives) - Impact of the MDR for Europe in Zurich,  Zurich, CH Zurich, Zurich, CH
2-day In-person Seminar: Introduction to Adaptive Design for Clinical Trials
  • In-Person Event-3 In-Person Event
  • Speciality Research and Clinical Research
  • Calendar Nov 15 - 16, 2018
  • 2-day In-person Seminar: Introduction to Adaptive Design for Clinical Trials in Philadelphia,  Pennsylvania, USA Philadelphia, Pennsylvania, USA
2-day In-person Seminar: Quality by Design - Essential Techniques for Medical Devices
  • In-Person Event-4 In-Person Event
  • Speciality Quality Management, Healthcare Management
  • Calendar Nov 12 - 13, 2018
  • 2-day In-person Seminar: Quality by Design - Essential Techniques for Medical Devices in San Diego,  California, USA San Diego, California, USA
2-day In-person Seminar: OSHA Recordkeeping and Surviving an OSHA Audit
  • In-Person Event-5 In-Person Event
  • Speciality Healthcare Management, Medical Education
  • Calendar Nov 08 - 09, 2018
  • 2-day In-person Seminar: OSHA Recordkeeping and Surviving an OSHA Audit in New Orleans,  Louisiana, USA New Orleans, Louisiana, USA
2-day In-person Seminar: Uncovering and Managing Successful Post Market Compliance for Medical Devices
  • In-Person Event-6 In-Person Event
  • Speciality Medical Education, Healthcare Technology ...
  • Calendar Oct 25 - 26, 2018
  • 2-day In-person Seminar: Uncovering and Managing Successful Post Market Compliance for Medical Devices in Philadelphia,  Pennsylvania, USA Philadelphia, Pennsylvania, USA
2-day In-person Seminar: SOP Writing, Training and Compliance in the Pharmaceutical Industry
  • In-Person Event-7 In-Person Event
  • Speciality Quality Management, Health Informatics ...
  • Calendar Oct 22 - 23, 2018
  • 2-day In-person Seminar: SOP Writing, Training and Compliance in the Pharmaceutical Industry in Arlington,  Virginia, USA Arlington, Virginia, USA