PharmaSys provides technical, quality and regulatory support and training to the pharmaceutical industry. Since 1998 we've been helping pharmaceutical, medical device, clinical research and biotech companies solve problems related to pharmaceutical and medical device development, manufacturing, analytical testing, validation, audits and quality systems.

We have a breadth of experience which enables us to support our clients in medical devices, combination products, solid dose, liquids, creams and sterile products and also API’s. Our technical knowledge encompasses small molecule, biological and plant based processes. We provide you with the solution to your problems on time and at a reasonable cost so you can run your business instead of troubleshooting.

PharmaSys operates on a global basis. We can provide on-going cost effective long term support for manufacturing and clinical organizations with limited in-house resources or technical expertise. We also provide support for turn-key projects ranging from developing CMC regulatory documentation for new products, transferring products, identifying and auditing new suppliers, developing GMP upgrades, ongoing engineering and operations and quality systems.

We also provide a manufacturing and quality interim management service in order to overcome short term resource issues caused by sudden but temporary increases in workload or loss of key staff.

PharmaSys has the knowledge and background to help you sustain your business.