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Pharmaceutical Cleanroom Validation Services | HVAC Systems

PDVD is established as one of the leading Cleanroom validation, Equipment qualification, Temperature mapping services provider company in india. We provide an extensive range of cleanroom validation, Equipment qualification, Temperature mapping services with all testing carried out to the highest standard by fully trained and competent engineers.

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Pharmaceutical Cleanroom Validation Services | HVAC Systems

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  1. PHARMACEUTICAL CLEANROOM VALIDATION SERVICES | HVAC SYSTEMS 01

  2. About Company As pharmaceutical cleanroom validation specialists, we at PDVD Consultancy can help you ensure that your pharmaceutical facility is operating as efficiently as possible. Pharmaceutical Cleanrooms are crucial places for several sectors, including biotechnology, microelectronics, and pharmaceuticals, where preserving air quality is crucial to product integrity. PDVD is established as one of the leading Cleanroom validation, Equipment qualification, Temperature mapping services provider company in india. We provide an extensive range of cleanroom validation, Equipment qualification, Temperature mapping services with all testing carried out to the highest standard by fully trained and competent engineers. 02

  3. Cleanroom Certification An official certification that the cleanroom satisfies the required cleanliness standards is known as a cleanroom certification. ISO 14644-1, which categorizes cleanrooms according to the number of particles permitted per cubic meter of air, defines these standards. The cleanroom is routinely inspected after certification to guarantee that the set standards are being followed. Need fast and reliable services for cleanroom validation pharmaceutical services in India? Connect with PDVD Consultancy for ISO 14644-1 cleanroom validation. 10

  4. Our Cleanroom Validation Services Facility Design and Layout 01 Installed Filter System Leakage Test 02 This test makes sure your cleanroom’s ULPA or HEPA filters are operating correctly. We use Poly Alpha Olefin (PAO) integrity testing to check for leaks and make sure the filters meet regulatory requirements. Test for Non-Visible Particle Counting 03 A thorough investigation of the cleanroom’s airborne particle levels is provided by our particle count test. In accordance with ISO 14644-1 and EU GMP requirements, the test is carried out in three different settings (As-Built, At-Rest, or Operational) to make sure the environment satisfies the necessary cleanliness level. 03

  5. Recuperation Exam Balance of Air Pressure 06 04 The recovery test calculates the speed at which a contaminated cleanroom can be cleaned up and restored to its initial state. This test is especially significant for sectors like pharmaceuticals, where ensuring rapid recovery times is essential. To avoid contamination, the proper pressure differential between cleanroom zones must be maintained. To ensure that the cleanroom keeps the necessary pressure levels, our professionals perform room pressurization tests. The Test of Containment Airflow Pattern Test (Using Water Fogger) 07 04 05 By using the containment test, you can make sure that particles in the air from nearby locations don’t get inside the cleanroom. We can assist you in keeping the cleanroom under control by finding possible leaks in the building’s structure. The Airflow Pattern Test uses water foggers to show the cleanroom’s airflow. Experts make sure that the cleanroom air is flowed evenly and that there are no spots around by using this test. We ensure that Air flow pattern in Clean room is Laminar and not turbulent, Also air flow is as per design pressure zoning between adjacent rooms from higher pressure to lower pressure zone (Room). 04

  6. Why Choose us for Pharmaceutical Cleanroom Validation Services in India? We, at PDVD Consultancy, are proud to provide thorough cleanroom validation services that are customized to your particular requirements. Our skilled group of experts is qualified to carry out all required examinations and assessments with accuracy and consideration. To maintain the efficiency and compliance of your cleanroom, we employ state-of-the-art machinery and follow industry guidelines. To make sure your facility complies with legal requirements and keeps a production environment under control, the cleanroom validation process is crucial. Certainly, PDVD Consultancy can assist you if you require continuous testing and monitoring or certification for a new cleanroom. You may be confident that your cleanroom will run as efficiently as possible with our professional services, safeguarding both your personnel and your products. 05

  7. Following are some of the reasons of our success: • Strong focus on quality compliance. • Timely delivery of physical service and support. • Provide effective document as per international guideline. • Physical presence and urgent document support provide during critical audit. • Service with answers “today” is our credo to support you with a fast and reliable service by specially trained service engineers to serve your specific needs. 06

  8. Our Contact +91 84691 49494 https://pd-vd.com/ info@pd-vd.com 09

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