Address: 211, Silver Coin, Shrenik Park Crossing, Productivity Road,
- Email: email@example.com
- Website: www.dagonpharma.com
- Phone No: +91 265-2321674
DAGON strictly follows Good Manufacturing, Laboratory and Documentation practices that ensures consistent high quality results. Our state-of-the-art analytical facilities monitors and maintains strict quality of our products, processes and services. This helps us to consistently meet IP, BP, USP quality standards.
Quality assurance comprises of Corporate QA and Site QA. Site QA is responsible for implementation of quality systems and release of all manufactured products. Corporate QA develops and ensures harmonization of all systems throughout the organization. It is also responsible for all audits including regulatory, customer, GMP, WHO, good laboratory practises and good documentation.
Highest quality standards are the key driver of success for any company. Effective quality control procedures are being carried out at different levels to maintain high standards. Quality control is responsible for all chemical analysis by DAGON. It also acts as a support during product development and validations. QC is supported by an experienced and qualified team of professionals.
Regulatory Affairs ensures compliance with the requirements of national and international authorities. This helps us to ensure that our products meet the required standards. Our regulatory affairs team develops regulatory strategy and integrates legal constraints into product development plans. Moreover department ensures that the firm adheres to the laws protecting public health.