QUALITY: FROM QMS TO INSPECTIONS
Quality is one of the core elements in pharmaceutical, medical device, and health care companies. This also means it shows up in a vast variety of places and steps along the way. You as our customer tell us how we can help you: We analyze your requirements, adapt the solution individually to your needs, and create a project plan. Then we carry out the project– together with you.
Prepare and perform audits and inspections:
A rising number of audits and inspections isn't only necessary to guarantee the safety and quality of your product: It's also legally required, and the regulatory demands are increasing. The experience in the field of quality as auditors, audited and inspection recipients of our experts will help you prepare for, perform and pass a large spectrum of quality controls.
Audit-As-A-Service
Feeling haunted by the audits you left unperformed? We help you to prepare for and perform audits.
This way you can assure the quality standard of purchased materials and services, and that you are in compliance with the ever more demanding regulations.
EU-GMP-As-A-Service
You want to offer your medicinal product on the EU market?
As a manufacturer, you need a corresponding certification, which you can obtain by passing a GMP inspection for your production facility. We assist you in getting the required EU-GMP certificate.
QP-As-A-Service
Overwhelmed by the amount of tasks as a QP and in quality management in general – or your circumstances don't allow you to fulfil all your obligations?
THE FORCE fulfils all functions of the Qualified Person for you and thus provides you with instant relief.
PV-Inspection-Readiness-
As-A-Service
Are you getting nervous whether you're safe to pass a PV inspection?
Our team at THE FORCE has specialized in supporting our customers to reach inspection readiness in Pharmacovigilance. We provide security to you!
Responsible-Person-For-GDP-
As-A-Service
Are you faced with the challenge of ensuring that your product reaches the patient in the same high quality in which it leaves you as the manufacturer?
We take care of quality control along the distribution channel.
MDR/IVDR-Compliance-
As-A-Service
The EU regulations on medical devices and IVDs have changed the requirements that manufacturers of medical devices have to meet.
Are you overwhelmed by the obligations these regulations bring along? We make sure that you implement them accordingly.