Algeria has the second largest pharmaceutical market in Africa.
- The pros and cons of drugs are not only directly reflected in the efficacy and safety, but also in the stability, consistency and practicality of the drugs.
- In order to ensure the quality of medicines, in addition to complying with relevant legal standards such as pharmacopoeia, it is very important to carry out production in a clean environment.
- Hazardous or non-hazardous foreign matter in the air of the production area should be minimized, and HVAC system will supply sufficient air to remove airborne particulates that may contaminate the product.
- The manufacturing process of sterile preparations consists of clean room areas from 10,000 to 100 level.
Clean room is an integral part of the manufacturing process required to produce sterile drug products, vaccines and bio-medical devices.
What do we do for Algeria Cleanroom Industry
RV-Cleanroom who has been a turnkey solution provider to the pharmaceutical manufacturing industry since 2002.
We provide a quality clean room project of pharmaceutical professionals with international standard capabilities.
Our pharmaceutical consultants can offer practical knowledge and experience on implementing or enhancing your Pharmaceutical Quality Systems (PQS) to meet GMP code requirements and those based on ICH Q10 / ISO 9001:2015 for Pharmaceuticals.
With 20 years of experience in the industry RV-Cleanroom has assisted many clients in various industries by providing air treatment solutions.