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   News & Events

28th Feb 2012: Sanhar is leveraged with Regional specific Regulatory Submission expertise and be able to help the customers in Multi Geographical Regulatory Submissions.

20th Feb 2012: Sanhar is an Associate Member of Indian Drug Manufacturers Association (IDMA), enabled with a gateway to reach out to more Domestic Customers now.

06th Jan 2012: Sanhar Joins hands with “Registrar Corp”, an U.S. based company to leverage its Regulatory Consulting services pertaining to the U.S. FDA Registration related Businesses.

 
 
 
 
   SANHAR Training Academy (Pharmaceutical Industrial Training Programs)
 

Personnel Qualification with appropriate Training to perform and supervise any specific activity/function is mandated as per the regulations. Moreover, training makes the people equipped to perform better. SANHAR’s industry experts would be providing the training and the participants would be issued a “Certificate” upon successful completion of the same.

We structured our training academy into two streams. One stream is to conduct the most reputed “Pharmaceutical Industrial Training and Career Development Workshop”, which helps the beginners and the Students of Chemistry, Pharmacy, Pharmaceutical Technology and related disciplines to get the awareness of the career opportunities available in the Industry. It is an Industrial Guide which provides the overview of the Industry, Pharmaceutical product life cycle, Regulatory requirements, high level understanding of the functions of the individual functional areas with more emphasize towards Current Good Manufacturing Practices. The participants would be provided with a “Certificate” upon successful completion which will definitely be an entry ticket for the beginners to kick start their Career dream.

The other stream focuses exclusively on the training requirements for the Pharmaceutical Industry & Life Sciences vertical IT professionals.

 
   We do conduct trainings and workshops on the following topics.
 
  • Pharmaceutical Industrial Training and Career Development Workshop – (Exclusively for the beginners/students)
  • Current Good Manufacturing Practices (cGMP)
  • Good Laboratory Practices (GLP)
  • Good Clinical Practices (GCP)
  • Good Documentation Practices
  • Risk Management
  • Computer System Validation
  • Integrated Validation Training Suite (Computer System Validation, Process Validation, Analytical Method Validation, Cleaning Validation and Instrument/Equipment Qualification)
  • Regulatory Submissions including eCTD concepts
  • Regulatory Affairs
  • Quality Assurance
  • Quality Management Systems
  • Quality Audits
  • Stability Study Management
  • CAPA Management
  • Regulations specific training on topics such as ICH, GAMP, ASTM, USFDA, EMA, TGA and any other related topics
  • Need based customized trainings on any topics related to Pharmaceutical Industry and so on.
  For your training needs, please write to “info@sanhar.in”
 
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Tel : +91 44 24921480
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