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The essence of Avesthagen's research and
development philosophy is productivity and flexibility anchored by
strict quality and safety controls throughout the organization.
Avesthagen follows good laboratory and documentation practices that
assure consistent high quality results that
exceed the expectations of the clients, business partners and regulators
meeting national and international quality standards.
Avesthagen's quality system
covers three key functional areas:
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Regulatory Affairs
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Quality Assurance
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Quality Control
Regulatory Affairs
is a
Corporate Division with a team of highly qualified & experienced
professionals who work pro-actively with all the four main strategic
business units of Avesthagen bioPharmaceuticals, bioNutrition,
bioAgriculture and Science & Innovation at every stage of the discovery
and development process to enable development for global markets. They
ensure that the research & development activities conducted in these
business units are in compliance with the requirements of national and
international regulatory authorities, and the data generated are of
internationally accepted quality to deal with the most stringent global
regulatory expectations. They provide training, interpret guidelines and
support early intervention for key regulatory decisions.
The primary function of Quality Assurance includes assuring
compliance with GLP, GMP and GCP requirements, implementation of quality
systems, inspections and checks during R&D and production activities.
Quality Assurance Division develops and ensures harmonization of all
systems throughout the organization. They adopt advanced quality systems
and undertake periodic audits and procedural documentation by monitoring
various activities of process research and production for regulatory
filing with national and international authorities.
Quality Control is responsible for
analytical support in the respective business units during product
development and validations, which helps us to deliver the quality
products.
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