Hospital Operating Room OEM Cleanroom Class 100 GMP Clean Room

OEM/ODM Service

01. Cleanroom design
In order to know your requirement, there's a structure condition table to fill in and supply CAD layout, so that we can provide correct scheme and quotation.
Our engineers and surveyors, supported by state - of - the - art computer systems, develop the graphic designs, attempting to adopt the best solution in order to optimize all the spaces, in accordance with the GMP guidelines.
GMP - review services can be provided by PHARMA CLEAN, even with the simple purpose of conducting a preliminary project overview.

02. Production and delivery
PHARMA has very strict control on the production link, and the operation department and the quality inspection department jointly supervise to achieve double verification and zero errors.
Before the goods leave the factory, they are assembled, spliced, and powered on to ensure that the customized products fully meet the standards in terms of quality and size.
This is because we are convinced that in our sector, in clean room construction, which is continuously expanding also from a competitive point of view, strict quality control is a key aspect which deserves utmost perseverance.
PHARMA CLEAN has invested heavily in new automation technologies for production, significantly reducing the factory processing times, whilst dedicating greater attention and time to the materials production phase. The strong increase in exports over the last decades has obliged us to steer our attention to our capability to monitor and track every single item produced and sold, in order to continue to minimize production and shipping errors.

03. Abroad Installation
The company has an installation team with full experiences in handling national and international projects, they have been to more than 30 countries.
We employ highly qualified staff with many years of experience in the construction of clean rooms. It is vital to emphasize our ability to provide direct installation services, at an international level, thanks to our teams specialized in the assembly of clean rooms. Guarantee of perfect execution and extremely accurate details.
PHARMA CLEAN currently boasts a high number of technicians for installation and supervision services, divided into 5 teams, for a total of 25 people. Direct collaborators (employees and freelancers), with continuous work relationships.

04. 24 hours on - line service
All customer will enjoy 24 hours pre - sale and after sale online service, build a discussing group that both salesman and engineer join us to answer your question and provide technical support.
PHARMA CLEAN is dedicated to keeping in contact with its customers even at the end of the installation of the material, and is always available for any future request.

In a pharmaceutical production packaging cleanroom designated as ISO 8, rigorous controls are in place to minimize
the introduction and spread of contaminants, ensuring the integrity and safety of the packaged pharmaceutical products.
This includes controlling air flow, using High-Efficiency Particulate Air (HEPA) filtration systems, maintaining strict
gowning procedures, limiting access, and regularly monitoring and testing the environment for particle counts and
microbiological contaminants. Despite being less stringent than some other cleanroom classifications, an ISO 8 cleanroom
still plays a vital role in preventing contamination that could compromise the efficacy or shelf life of pharmaceuticals.