PCS helps it's clients meet quality and regulatory requirements. We do this by training, advising and continuously checking your compliance level. Thereby guaranteeing that your company meets the GMP rules and regulations.
What is GMP?
Good Manufacturing Practice, also known by its common abbreviation "GMP", is a quality assurance system for the pharmaceutical industry. Only a carefully defined and controlled production process ensures the quality of a medicine.
Without a GMP license, also known as a "MIA" or Manufacturing and Import Authorization, drug manufacturers are not allowed to sell their products to pharmacies or hospital pharmacies.
Why choose PCS for GMP advice and training?
PCS helps clients to achieve the desired level of quality. We do this by providing GMP training. In addition, we can also be called in for GMP consultancy and we help you with the application for GMP licenses.
Our services range from implementation of quality systems, obtaining GMP licenses to interim management and training. Our approach is simple: understanding and mastering your process is key to GMP.
Supply chains are very complex, the quality department often has a full-time job keeping the quality system up-to-date and production struggles to meet demand. PCS comes to the rescue to ensure that everything goes according to the right guidelines.
Customers choose PCS because of our extensive regulatory experience. Time always plays a role in our projects. We know how the authorities work and what they expect. In this way we bring our clients to a higher level of GMP compliance efficiently, within time and within budget. Thanks to our team of passionate consultants, consisting of ex-EU GMP inspectors and leading industry experts, we can provide this unique service to the pharmaceutical market.