Master analytical method development, impurity profiling, and reference standard preparation
Key Learning Highlights:

• Analytical method development & validation (Assay, Related Substances)
  
• Impurity isolation & characterization using HPLC, GC, UV
  
• Reference Standard preparation for regulatory compliance

This program is ideal for those looking for an analytical research and development course in Pune that combines scientific rigor with practical expertise.

Build robust QA competence in GMP, GLP, SOPs, audits & documentation
Key Learning Highlights:

• Regulatory guidelines: cGMP, GLP, GDP, 21 CFR Part 11, ICH Q7
  
• Change control, OOS/OOT handling, IPQA, deviation and market complaint management
  
• Drafting SOPs, document control, QMS and internal auditing skills

Our QA program is one of the best quality assurance pharmaceutical courses, focusing on compliance, regulatory audits, and documentation aligned with pharmaceutical quality management system in Pune standards.

Learn process optimization, scale-up techniques & chromatographic validations
Key Learning Highlights:

• Literature review & feasibility study design
  
• Process optimization & lab-scale validation
  
• Scale-up strategies, column chromatography, TLC method development

This course equips you for research and development in the pharmaceutical industry, with real exposure to process validation and scale-up practices.

Understand plant-level GMP manufacturing, cleaning validation & batch record keeping
Key Learning Highlights:

• Operations under cGMP in a pharma manufacturing setup
  
• Batch Manufacturing Record management
  
• Process and cleaning validation essentials for compliance

If you’re aiming to work in large-scale production units, our pharmaceutical manufacturing course prepares you for plant-level roles in production, compliance, and quality.