Vyacheslav Krauklis obtained a bachelor’s degree in Biology and a master’s degree in Chemistry from the State University of Latvia. He started his career as an analyst and chromatography specialist at the analytical laboratory. After that, he graduated from the Master’s professional program “Total Quality Management” at Riga Technical University and was an associate professor for several years there. He has the experience of being an ISO auditor and GMP inspector at the regulatory body of Latvia as well as at the EMA, WHO and PIC/S. Since 2010, he has been working as Quality Director at the production sites of the chemical API and non-sterile pharmaceutical forms, as well as biotechnological API and sterile pharmaceutical forms since 2013. During his career, he has successfully carried out more than 50 regulatory audits and inspections as well as GMP inspections of INVIMA, WHO, FDA and European agencies. He has continued in self-education, obtaining his Master’s degree in Pharmacy at the Medical Academy of Latvia. He regularly participates in the conferences and workshops in the Russian Federation, Europe and the USA. He has never refused to help and to consult on any production site.