Inofar
GMP Audit

Pharmaceutical innovation policy that provides complete solutions for the pharmaceutical industry INOFAR Ltd.. Sti. In other activities, as well as GMP, GLP, GCP'ye suitability to control and monitor the external audits and internal controls that provide service in the field.Representation of origin and in many countries have undertaken to provide this service in Spain continues to control the activitiesthrough which firms are realizing the TDV. Summary informationabout our services, are summarized below:

• Supplier GMP inspections
• FDA, EU controls preparation
• Training programs
• Computerized system validation
• compliance with good clinical practice and pharmacovigilance

Especially in India and China in order to evaluate the active ingredient supplier, GMP, cGMP needs to be done every 3 yearsaccording to the Audit active ingredient manufacturer for more than 35 companies so far (Far East) has been prepared on behalf of the GMP Audit Report, according to the reports you request share it would like to state. In this way, the active ingredient in one singlesupplier and a significant reduction in the cost of the GMPSupervision of implementation of the audit will be provided morequickly.

Spain Pharmaceutical Industries such a Supplier - GMP InspectionCooperation was held successfully, the control model in Turkey, we are ready to implement and enforce.

Services (All)
İnofar
2146 Sok No: 5/4 06510 Çankaya ANKARA TURKEY, P: +90 (312) 4727221 - F: +90 (312) 4727251, info@inofar.com
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