The demands of the markets is such that every client needs to be constantly updated to maintain the competitive edge in par with changing regulations of different Regulatory Authorities.

Given the pre-occupation of the professionals, Mediviz provides training, aimed to appraise the organization on the new legislation/s and provide guidance on GMP in the pharmaceutical industry.

In the course of its training, Mediviz exhorts clients to understand the role of inter-departmental QMS controls in the entire pharmaceutical supply chain and how to effectively document and continually improve the systems in place to ensure GMP compliant standards.

Training modules are designed for individuals representing Quality Assurance, Quality Control, Production and Management. Designing, developing and delivering targeted GMP training to audiences ranging from line operators to management is Mediviz’s forte.  Individuals of all levels within a Pharmaceutical manufacturing organization/Pharma educational Institution will benefit by understanding the GMP requirements.

Mediviz training sessions are characterized by the participation of eminent trainers and speakers on GMP/Regulatory/Analytical and Managerial topics. Expert speakers from Pharmaceutical Industry and allied fields will also be invited to conduct training on contemporary challenges and topics.

Training includes

  • On-Site training on basic cGMP concepts/ Regulatory updates/ Regulatory Authority observations.
  • Quality/Regulatory Training
  • Audit Training