Quality assurance
We aim to exceed all expectations related to the quality of services we provide and to ensure that our clients recieve the highest level of service.
iPharma successfully conducts various clinical trials (innovative, biological drugs, bio analogues and generic drugs), including supervisory programs for clients around the world.
Our quality management services include:
- consultations and recommendations related to topics of quality and compliance with requirements;
- audits of clinical platforms;
- audits of clinical trial providers;
- development of standard operating procedures (SOPs) for clinical operations;
- support of activities on specific projects.
SOP
iPharma has an extensive system of standard operating procedures (SOPs) which ensure that our employees’ work is efficient and our production quality is maintained. SOPs also establish a sequence of actions, which eliminates the possibility of misunderstandings or non-compliance with industry regulations. All activities are carried out in strict accordance with applicable procedures.
Furthermore, all SOPs are regularly reviewed to ensure their relevancy and also can be reviewed within our company or as per the Sponsor’s requests.