Quality Management is the cornerstone of Pharmaceutical Manufacturing
Making sure a pharmaceutical company operates in a GMP compliant way is one of the main daily activities the company has to deal with. In routine manufacturing, in expansion projects, in launching new products but also in R&D and clinical development.
Appropriate Quality Management ensures this day to day compliance.
You do not always have the time, resources, experience or knowledge to fulfil this task.
We take care
Syntiro can help you with this important task.
Provide experienced interim resources when needed for Quality Assurance and Qualification/Validation.
When you are a start-up, we can help you setting-up a compliant Quality System.
Design and execution of qualification and validation studies.
Document writing for Quality System or Regulatory requirements.
Perform or prepare for audits (client, supplier, regulatory).
Training of staff (GMP, GDP, GLP).
Not only identifying non-compliant issues but also resolving them.
Advanced therapies, API manufacturers, Biotech, Cell & Gene, Fill & Finish, Logistics, Solids manufacturing, Sterile manufacturing, Veterinary medicine.