Why Sterile Packaging Standards Matter in Indian Pharma

Sterile packaging is the last line of defence between a contaminated product and a patient. Yet it is often an afterthought in pharma manufacturing. This article explains why it should be a priority.

KEY POINTS TO COVER:

• What is sterile packaging and why does it matter
• Regulatory requirements — Schedule M, ISO 11607, WHO GMP
• Common failures in Indian pharma sterile packaging
• What to look for in a sealing machine and packaging material
• How validated packaging reduces recalls and regulatory risk