DVACI

DVACI Expertos en detección de fugas y hermeticidad para packaging. Cámaras de vacío CDV que garantizan calidad en envases farmacéuticos, médicos y alimentarios

02/04/2026

At DVACI, we’ve developed a specific AI prompt tool to help define the appropriate vacuum level for each packaging type. By entering your packaging and test condition data, it automatically suggests recommended parameters. Fill out our contact form on our website, if you want to receive this prompt.
👉🏼 Want to send us your samples? Complete our contact form:
📩 https://dvaci.com/contact/ we’ll perform a free demonstration and send you our personalized recommendations.
🔬 DVACI – Leak Testing Solutions for the Pharmaceutical and Medical Industries📍 Learn more at 👉 https://dvaci.com

31/03/2026

How much vacuum can you apply to detect real leaks — without deforming or damaging the package?
At DVACI, we recommend applying approximately 70% of the failure level as your operational vacuum. This provides sufficient pressure differential to reveal leaks without compromising product integrity.
👉🏼 Want to send us your samples? Complete our contact form:
📩 https://dvaci.com/contact/ we’ll perform a free demonstration and send you our personalized recommendations.
🔬 DVACI – Leak Testing Solutions for the Pharmaceutical and Medical Industries📍 Learn more at 👉 https://dvaci.com

26/03/2026

What the ASTM D3078 Actually Says?
The standard does not define specific vacuum levels or exposure times, because every package behaves differently depending on size, material, and mechanical strength. That is why each user must establish their own parameters. This is where the practical methodology we use at DVACI becomes essential.
👉🏼 Want to send us your samples? Complete our contact form:
📩 https://dvaci.com/contact/ we’ll perform a free demonstration and send you our personalized recommendations.
🔬 DVACI – Leak Testing Solutions for the Pharmaceutical and Medical Industries📍 Learn more at 👉 https://dvaci.com

24/03/2026

In the pharmaceutical industry, we all share one responsibility: ensuring that every sterile package maintains its integrity until final use. A leak is not just a defect—it is a regulatory nonconformance, a risk to the patient, and a problem no one wants to face.

Here is a tip that almost no one applies and that can significantly improve test reliability: perform a maximum pressure test, or burst test.

👉🏼 Want to send us your samples? Complete our contact form:
📩 https://dvaci.com/contact/ we’ll perform a free demonstration and send you our personalized recommendations.

🔬 DVACI – Leak Testing Solutions for the Pharmaceutical and Medical Industries📍 Learn more at 👉 https://dvaci.com

19/03/2026

In the pharmaceutical industry, we all share one responsibility: ensuring that every sterile package maintains its integrity until final use. A leak is not just a defect—it is a regulatory nonconformance, a risk to the patient, and a problem no one wants to face.

Once the test pressure has been defined, the next step is to establish the observation time, using the Control Sample as the minimum reference.

👉🏼 Want to send us your samples? Complete our contact form:
📩 https://dvaci.com/contact/ we’ll perform a free demonstration and send you our personalized recommendations.

🔬 DVACI – Leak Testing Solutions for the Pharmaceutical and Medical Industries📍 Learn more at 👉 https://dvaci.com

17/03/2026

In the pharmaceutical industry, we all share one responsibility: ensuring that every sterile package maintains its integrity until final use. A leak is not just a defect—it is a regulatory nonconformance, a risk to the patient, and a problem no one wants to face.

Each laboratory must establish its own test pressure and holding time at pressure, using a validated methodology. This is where the Control Sample becomes essential.

👉🏼 Want to send us your samples? Complete our contact form:
📩 https://dvaci.com/contact/ we’ll perform a free demonstration and send you our personalized recommendations.

🔬 DVACI – Leak Testing Solutions for the Pharmaceutical and Medical Industries📍 Learn more at 👉 https://dvaci.com

12/03/2026

In the pharmaceutical industry, we all share one responsibility: ensuring that every sterile package maintains its integrity until final use. A leak is not just a defect—it is a regulatory nonconformance, a risk to the patient, and a problem no one wants to face.

How do we define the correct test pressure and the appropriate time to reveal real leaks without damaging the package?

👉🏼 Want to send us your samples? Complete our contact form:
📩 https://dvaci.com/contact/ we’ll perform a free demonstration and send you our personalized recommendations.

🔬 DVACI – Leak Testing Solutions for the Pharmaceutical and Medical Industries📍 Learn more at 👉 https://dvaci.com

Leak… or expanding internal air?This is one of the most common misinterpretations in bubble testing.True leaks show:• Co...
10/03/2026

Leak… or expanding internal air?

This is one of the most common misinterpretations in bubble testing.

True leaks show:
• Continuous emission
• Seal-origin pattern
• Repeatability

Misreading bubble formation can lead to false rejects — or worse, false passes.

Would your team get this right?

👇 How do you train operators to distinguish the difference?

—

If you want confirmation under controlled vacuum conditions,
send us your samples and we’ll test them.
👉🏼 https://www.dvaci.com/contact/

A $0.02 seal defect can become a $200,000 recall.Seal contamination.Channel leaks.Delayed detection.Integrity failures s...
05/03/2026

A $0.02 seal defect can become a $200,000 recall.

Seal contamination.
Channel leaks.
Delayed detection.

Integrity failures scale fast because they travel through distribution, storage, and time.

By the time they’re discovered, the damage is already done.

Have you ever seen a recall start this small?

👇 What was the root cause?

—

Want to verify your seal integrity before it becomes a liability?

Send us your samples.
We’ll run controlled vacuum testing and provide visual evidence.
👉🏼 https://www.dvaci.com/contact/

HOPE is not a test method.Squeeze tests.Visual checks.Sound-based assumptions.They’re common.They’re risky.Integrity req...
03/03/2026

HOPE is not a test method.

Squeeze tests.
Visual checks.
Sound-based assumptions.

They’re common.
They’re risky.

Integrity requires controlled pressure differentials and repeatable evidence — especially when compliance, shelf life, or sterility are on the line.

What test method do you still see “in the wild”?

👇 Drop it in the comments.

—

Not sure your current method is catching micro leaks?
Send us your samples and we’ll test them for you.
👉🏼 https://www.dvaci.com/contact/

This package passed inspection.Until it met differential pressure.Most leaks don’t look like leaks.They look compliant.V...
26/02/2026

This package passed inspection.
Until it met differential pressure.

Most leaks don’t look like leaks.
They look compliant.

Visual checks validate appearance.
Vacuum testing validates integrity.

If you’re relying on surface evaluation alone, you may be missing microchannels, seal contamination, or hidden integrity failures.

Would this pass in your plant?

👇 Tell us your current leak test method.

—

Want a second opinion?
Send us your samples and we’ll test them under controlled vacuum conditions.

👉🏼 https://www.dvaci.com/contact/

16/02/2026

The third evolution is testing capability. The new CDV Pharma now supports dye pe*******on testing under both vacuum and pressure. Pressure testing is available in two configurations:

- Internal pressurization, in accordance with ASTM F2096,
- External pressurization, which significantly increases sensitivity by actively forcing dye into potential defects.

With the same system, you can perform vacuum-only tests such as ASTM D3078, internal pressure tests, and combined vacuum and pressure methods.
One instrument, multiple test standards..
🔎 CDV Pharma is a high-precision leak testing system for pharmaceutical packaging integrity, engineered to meet laboratory demands for accuracy, flexibility, and full traceability. Its latest redesign adapts to evolving pharmaceutical packaging formats, enabling vacuum and pressure-based dye pe*******on testing in full compliance with international standards such as ASTM D3078 and ASTM F2096.
📌 With the new CDV Pharma, you can now perform multiple pharmaceutical packaging integrity tests using one single instrument:
Vacuum-only leak testing (ASTM D3078).
Internal pressure testing (ASTM F2096).
External pressure testing for increased detection sensitivity.
Combined vacuum and pressure methods for enhanced reliability.
👉 One instrument. Multiple test standards. Maximum flexibility for pharmaceutical laboratories.
🌐 Learn more about the CDV Pharma system and explore its full technical specifications:
👉 https://dvaci.com/cdv-pharma/
👉🏼 Want to send us your samples? Complete our contact form:
📩 https://dvaci.com/contact/ we’ll perform a free demonstration and send you our personalized recommendations.
🔬 DVACI – Leak Testing Solutions for the Pharmaceutical and Medical Industries📍 Learn more at 👉 https://dvaci.com

Address


Opening Hours

Monday 09:00 - 18:00
Tuesday 09:00 - 18:00
Wednesday 09:00 - 18:00
Thursday 09:00 - 18:00
Friday 09:00 - 18:00

Telephone

+524421935630

Website

Alerts

Be the first to know and let us send you an email when DVACI posts news and promotions. Your email address will not be used for any other purpose, and you can unsubscribe at any time.

Shortcuts

  • Want your business to be the top-listed Equipment Service?

Share