Services

The pharmaceutical industry is strictly regulated by governmental bodies such as the FDA, EMEA and IGZ. The most important rules have been recorded in the GMP (good manufacturing practices) guidelines.

Every pharmaceutical production company needs to ensure that they have a validation programme for all critical facilities, installations and equipment involved in the production process. In validation we prove that the procedure, process, device, material, activity or system does indeed do what it is supposed to do. This is a time-consuming exercise that requires a multildisciplinary approach. In addition, excellent organisation and documentation are needed to maintain an overview of responsibilities and activities.

IPCVS provides the following services to support you in your project, ensuring compliance with the relevant rules and guidelines:

Consultancy

IPCVS provides high quality consultancy services for projects related to commissioning, validation and engineering of equipment, processes and facilities.

Project Management

IPCVS will manage your project from start to finish. We assist you with initiating the required documentation such as validation master plans, project plans, user requirement specifications (URS), commissioning- and validation protocols. We also support you by executing the actual commisioning and validation activities.

Documentation

IPCVS assists with the adjustments of existing documents or the creation of customised protocols, work instructions or standard operating procedures (SOP) in both Dutch and English.