Eugia: ScanStation testimonial

Published on 29 February 2024 Eugia: ScanStation testimonial

Eugia US Manufacturing LLC is a subsidiary company of Aurobindo Pharma. It is a US-based independent pharmaceutical company focused on generic sterile injectables, hormones, oncology and ophthalmic medicines to cover the market globally.

Location: East Windsor, New Jersey (USA)

Works with: Scan 100 / ScanStation 300, real-time incubator and colony counters

Logo Eugia

Mr. Nilkantha Banerjee, Head of Microbiology, and his team offer a ScanStation testimonial exploiting the benefits of integrating the ScanStation into the Pharmaceutical industry.

How does automating microbiological analyses with ScanStation improve your laboratory 21 CFR compliance?

"Based on my review of the past 11 years data of the FDA Inspection Observations, the top 5 FDA 483 given for CFR violations in Microbiology were:

21 CFR 211.160(b) Scientifically sound laboratory controls

21 CFR 211.113(b) Control of Microbiological Contamination

21 CFR 211.110(a) Control Procedures to monitor and validate performance

21 CFR 211.165(a) Testing and release for distribution

21 CFR 211.63 Equipment Design, Size and Location

The highest number of observations were given for 21 CFR 211.160 (b). Scientifically sound laboratory controls. ScanStation 300 can mitigate these observations with early detection. The plates are read every hour, giving real-time colony counts with pictures. This robotic incubator will ensure that data integrity is followed with its 21 CFR Part 11 compliant software and ensures there is no data falsification.

Data assurance is achieved through the review and approval process. ScanStation 300 is greatly improving laboratory 21 CFR compliance and control. I believe ScanStation is revolutionary for the pharmaceutical industry."

Nilkantha Banerjee - Head of Microbiology, Eugia US Manufacturing LLC

Eugia US Manufacturing LLC is a generic injectables company and its mission is to produce affordable products to solve people health issues. The facility manufactures generic injectables products to cover the market globally. Eugia US Manufacturing LLC was the first company in the United States to introduce the ScanStation, a real-time incubator and colony counter, in the pharmaceutical industry. Environmental Monitoring samples from Aseptic Filling Area classified as ISO 5 / Class 100 / Grade A are analyzed to guarantee environmental control and monitor product quality.

Why use ScanStation?

How did you hear about the ScanStation?
And, why did you feel the need for automation?

 ScanStation 300 (Ref. 439 300) - Real-time incubator and colony counter

Nilkantha Banerjee:

I discovered ScanStation in 2015 through my personal research when trying to find equipment that can automate processes in pharmaceutical microbiology. I heard that this equipment was being used in the food industry, but I wanted it to be incorporated in the pharmaceutical industry. I introduced ScanStation in the US pharmaceutical industry in 2019.

“ I believe automation is needed to mitigate violations with 21 CFR 211 by allowing real time analysis of plates during the incubation process.”

How does the ScanStation change your work?

Nilkantha Banerjee:

ScanStation is very useful for understanding when the first colony appeared and on which location of the plate. It is important, especially for a plate with fungus.

Nilkantha Banerjee and his team:

ScanStation complies with CFR providing real-time data. It increased traceability and reliability of data. Early detection of presence of organisms in critical areas allows for early remedial actions for products, preventing monetary loss, and saving brand value.

We are monitoring all our ISO 5/ Class 100/Grade A EM plates in the ScanStation. The acceptance criteria is less than 1 CFU. If a colony appears, we can notify the required personnel and start investigation to find the root cause. If microbial growth begins in these plates before our sterility results are obtained, it is crucial to halt the subsequent levels of manufacturing and product distribution. This applies to products that were manufactured before, during and after this EM monitoring occurred. This is essential for operational safety and compliance with regulations and the data obtained adheres to 21 CFR Part 11 compliance, ensuring an Audit Trail and preventing any possibility of data falsification.

The feature that I like the most is that the ScanStation is a real-time incubator and colony counter and it allows to take corrective actions in a timely manner if needed.

It gives us the “back in time video”, which we can check during the incubation or even after.

ScanStation hardware and software are very user friendly.

How was ScanStation introduction into your workflow?

Nilkantha Banerjee and his team:

We validated the ScanStation as per our internal validation program. We did not have to change our usual protocol. We use the same media for all our incubators.

ScanStation is used daily for ISO 5 / Class 100 / Grade A Environment Monitoring. We use the “Result & Approval” module which allows a dual validation by two different Microbiologists. It brings to us data accuracy because we check the plates manually and compare with the ScanStation count during the review and approval process. If the release of plates falls on a weekend or holiday, the review and approval happen on the next working day. However, the colony counts and images automatically stop after the incubation period ends.

How do you manage the traceability of your samples?

Nilkantha Banerjee and his team:

The ScanStation helps us to keep traceability. We really like this system because of our core values: honesty, integrity and transparency are met. We feel very comfortable of having implemented the ScanStation in our microbiological workflow. Because after all, we all work for patient safety and quality medicine.

To trace our samples, we use the unique ID number given by the ScanStation (Plate ID No) and we write it down on our test data sheet.

PROTOCOL OF ANALYSIS:


Environmental Monitoring (EM) for ISO  5 / Class 100 / Grade  A on settle plates and air sampling plates.

Number of samples per day: 100 or more
Microorganisms analyzed: Environment Isolates
Medium used: Soyabean Casein Digest Agar (SCDA)
Incubation time: 120 hours (5 days)
Incubation temperature: 20-25°C or 30-35°C
Program used (pre-set /custom): ScanStation Pre-set

Why choose Interscience?

Nilkantha Banerjee:

We chose Interscience because of its innovative technology. Interscience is an innovator that was able to create revolutionary equipment in the microbiology field.

Nilkantha Banerjee:

The above testimonial is strictly my views based on my experience and does not represent the views held by the company with which I am affiliated.