RegEnd has team of expert professionals who performs third party evaluation (Gap analysis) of pharmaceutical manufacturer. We offer a full range of services in GCP, GLP and GMP compliance from development through commercialization. We help pharmaceutical company to implement comprehensive CAPA and prepare them for various Regulatory authority inspection.

• Execution of green field project of finished dosage form.
• People management through training
• Equipment Qualification and Validation
• Process control and Validation
• PLC Validation
• Utility Qualification and Validation
• Computer system validation
• Vendor qualification
• People development through training
• Process Control and validation
• GXP Compliance support
• QMS implementation