Gain hands-on understanding of analytical method development, regulatory documentation, AI-driven insights, and practical problem-solving — all guided by an experienced industry professional.

Whether you’re a student, graduate, or professional looking to advance, this program helps you understand how the pharmaceutical industry really works — from lab data to regulatory submissions.

Session Options

• Free Consultation (15 min) – Get a quick introduction, discuss your goals, and see how the program can help.
• 1:1 Mentorship / Career Session (30–60 min) – Personalized guidance on analytical development, regulatory documentation, or career planning

Program Highlights

• Analytical Method Development, Method Validation and Method Transfer.
• Formulation & Drug Product Understanding.
• Clinical & Development Context.
• Regulatory Writing – preparing 3.2.P sections, method validation reports, and analytical summaries.
• AI Applications in Analytical Development & QC.
• GMP Compliance, Quality Systems, and Investigations (OOS/OOT).
• Career Mentorship & Job Readiness.

• Live, interactive sessions (online)
• Case studies from real projects
• Assignments and discussion-based learning
• Optional 1:1 mentorship

• Hands-on Analytical Skills – Method development, validation, dissolution, solubility, and discriminative studies
• Regulatory Expertise – Preparing 3.2.P sections, validation reports, and analytical summaries
• AI Applications – Using AI for method optimization, data analysis, and QC insights
• Career Readiness – Resume optimization, LinkedIn review, interview guidance, and career path mapping
• Practical Tools & Templates – Real-world examples including method development reports, validation protocols, and regulatory documentation
• Certificate of Completion – Verified recognition of your participation and learning