
The 2nd Edition of the Steriles & Injectables India Summit 2026 brings together industry leaders, regulators, technology providers, and quality professionals to address the evolving landscape of sterile and injectable drug manufacturing. As injectables continue to dominate critical therapeutic areas, the industry faces growing challenges
The 2nd Edition of the Steriles & Injectables India Summit 2026 brings together industry leaders, regulators, technology providers, and quality professionals to address the evolving landscape of sterile and injectable drug manufacturing. As injectables continue to dominate critical therapeutic areas, the industry faces growing challenges around aseptic processing, regulatory compliance, packaging integrity, and maintaining uncompromised quality.

This summit serves as a focused platform to explore manufacturing innovation, regulatory preparedness, and quality assurance strategies shaping the future of sterile and injectable products. With increasing scrutiny from global regulatory authorities and rapid adoption of advanced technologies, organizations must rethink traditional appro
This summit serves as a focused platform to explore manufacturing innovation, regulatory preparedness, and quality assurance strategies shaping the future of sterile and injectable products. With increasing scrutiny from global regulatory authorities and rapid adoption of advanced technologies, organizations must rethink traditional approaches to ensure patient safety, operational excellence, and sustainable growth.

Through expert presentations, panel discussions, and knowledge-sharing sessions, the summit will delve into next-generation sterile manufacturing practices, Pharma 4.0 adoption, regulatory expectations, injectable packaging innovations, and quality risk management. The event aims to provide actionable insights, real-world case studies, an
Through expert presentations, panel discussions, and knowledge-sharing sessions, the summit will delve into next-generation sterile manufacturing practices, Pharma 4.0 adoption, regulatory expectations, injectable packaging innovations, and quality risk management. The event aims to provide actionable insights, real-world case studies, and strategic perspectives to help organizations stay compliant, competitive, and future-ready.














Head Injectable,
Aurobindo Pharma

Head Quality,
Naprod Life Sciences

Sr. V.P. MF,
Amneal Pharmaceuticals

Senior Technical Advisor,
Indian Pharmaceutical Alliance

Head Compliance (Sterile), Sun Pharmaceutical Industries Limited

Sterile Manufacturing Site Director,
Centrient Pharmaceuticals

Vice President & Head-Drug Product Manufacturing, Biological E Limited

Former Sr. Vice President, Cadila Pharma Ltd

Plant Head (Sr GM), Immacule Lifesciences (Acme Group)

Biopharma Quality Consultant

GM,
Kashiv BIosciences

Independent Director,
IOL Chemicals & Pharmaceuticals Ltd.








Topic: India’s Steriles & Injectables Growth Story: Regulatory Expectations, Capacity Expansion & Global Trust
Topic: Practical Implementation Challenges & Learnings from Indian Facilities
Topic: Visual Inspection in Injectables: Manual, Semi-Automated & Fully Automated Approach
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