Vasa Pharmachem has a complete Quality Management and Production Management systems through Quality Control department who strictly follow cGMP standards and strict In-house quality standards.
Test and Retest are carried out on the facility equipments and production methods. The QMS of Vasa Pharmachem which ensures high quality standards.
Internal checks are conducted on regular basis to ensure constant improvement. This is ensuring the quality and safety of the product.
The inspections take place in conformance with the certification documentation, with due consideration of the status of science and technology as well as the current requirements on the field of pharmacopoeia and GMP Directives. Inspections are carried out on qualified devices using validated methods. Raw data is recorded without gaps. It is ensured that raw data, test reports and other related material is archived.
Delivering the best regulatory compliant products
Beyond manufacturing, we stand by our clients and simply their compliance measures. Having had long experience of delivering solution that meets various regulatory requirements, including 17 Products haveing USDMF registration, we are adept to deliver the following regulatory support
Stability Data as per ICH Guidelines
Residual Solvent as per ICH Guidelines
Technical Data Package in CTD format for all products
Declarations available as per Global Regulations
Specs, MOA and MSDS as per current Global Standards
Preset VAQ for all customers as per Global Standards for better customer service