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Strategic Partnership Ampoule CPHI Milan 2026Hall 11, Stall K836 to 8 October

Quality

Quality we never leave to chance.

From the first glass tube to the final pallet, every Ampoule, Vial and Cartridge passes through certified systems, automated inspection and full batch traceability. It is how Shree Naina Glass Inc. has kept a record of zero customer recalls.

Automated glass handling line with a robotic arm

From tube to dispatch

Five checkpoints between the furnace and your filling line.

Quality is not a final test. It is built into every stage, so problems are caught where they start.

Glass containers moving on an automated production line
Robotic handling with no human touch
  1. 01

    Qualified Type I tubing

    First hydrolytic class borosilicate glass, bought only from suppliers who pass a strict check of credentials and performance.

  2. 02

    Controlled forming

    Forming temperature watched with pyrometers and forming speed monitored continuously, with statistical in-process controls.

  3. 03

    100% camera inspection

    Every single piece is checked online for dimensions and cosmetic defects, so quality never depends on sampling.

  4. 04

    Robotic handling

    A robotic system picks each piece, so no human hand ever touches the glass.

  5. 05

    Secured storage and lot clearance

    Finished goods wait in a controlled store until dispatch, with a lot clearance certificate for every shipment.

Certifications and approvals

Recognised by the standards that matter to you.

Each certificate below is held by Vielfys, by Shree Naina Glass Inc. or by both companies.

  • ISO 9001

    Quality management, held by Shree Naina Glass Inc. since 1996

    Vielfys and SNG
  • ISO 9187

    Glass Ampoules for injectables

    Vielfys
  • ISO 15378

    GMP for primary packaging materials of medicines

    SNG
  • cGMP

    Current good manufacturing practice in every factory

    SNG
  • USFDA DMF

    Drug Master File with the US Food and Drug Administration

    SNG
  • Health Canada DMF

    Drug Master File with Health Canada

    SNG
  • NMPA DMF

    Drug Master File with the National Medical Products Administration, China

    SNG
  • EcoVadis Silver

    Sustainability rating, in the top 15% of companies assessed

    SNG

Batch traceability

One number follows every lot, from raw material to your dock.

Each production lot opens with its own batch record that captures every variable on the line. Its unique number is never reused and travels with the lot through every document and label.

With that number we can trace the raw material, the line start and end times, the operator, the QC supervisor, the shift technician and the warehouse team. Records are kept for five years after dispatch.

Your lot number

  1. Order confirmation
  2. Transport document
  3. Invoice
  4. Box label
  5. Pallet label
  6. Screen print film
  7. Certificate of lot clearance

Our quality team

People who make quality their whole job.

Professionals drawn from the pharmaceutical industry run our procedures, audits, inspections and training, with every team member trained continuously and certified by QA.

18

Quality team members

Across three factories

5

Lab resources

Spread across our sites

1

Dedicated QA manager

Leading quality assurance

5

Years batch records are kept

After every dispatch

0

Customer recalls

A clean record to date

1996

ISO 9001 since

Shree Naina Glass Inc.

Regulatory support

Paperwork that helps your submissions move faster.

Packaging has a direct effect on the medicine inside, so regulators look at it closely. Our team makes that part of your work easier.

  • Letter of Authorization

    Every customer receives an LOA free of charge and on time.

  • DMF letters of access

    Drug Master Files on record with the USFDA, Health Canada and the NMPA.

  • Certificates of analysis

    Sample certificates on request, so your team can review them in advance.

  • Close to the standards

    Our regulatory team takes part in FEVE, PDA and AFNOR committees.

Need documents for an audit or a submission?

Ask for DMF letters of access, an LOA or a sample certificate of analysis. Our team will send what you need.