We provide quality management services to ensure effective process in compliance with latest regulatory requirements, and guidelines.
We support our clients with routine and ad-hoc oversight of quality of the clinical trial conduct and Pharmacovigilance processes through customized approach designed, defined and adhered in line with our client requirements in demand.
As an integral part of merger and acquisitions, our Quality assurance experts support due diligence and recommend measures to facilitate smooth transition complying with standards and requirements.
Pharmacovigilance and clinical research experts with Quality assurance and auditing acumen facilitate audit of Pharmacovigilance System and clinical trials status quo and support in enhancing the system vis-a-vis the current global regulatory requirements.
We can help in establishment of robust Pharmacovigilance system compliant with latest regulatory requirements, compliance monitoring, CAPA management, development of standard operating procedures, training and development.
Experience in handling Audit and Inspection.
Familiar with global guidelines and regulations.
Effective systems in compliance with regulatory requirements.
Equiped with latest technology and tools.