NutrivaGlobal specializes in offering finish formulation, analytical development, stability & scale-up services for all dosage forms.We strive to identify, meet and exceed our customer’s quality requirements through Current good manufacturing practices.Our Quality Policy is based on the following principles:
- Technical Know-how and Execution: All the processes are implemented as per the SOP (Standard Operating Procedures) and
internationally certified manufacturing standards. - cGMP: All the processes and activities are in total compliance with cGMP principles.
- Authentication/ of Documents: Retrieval, validation, and verification of data and documents of our processes and products; is guaranteed at all times due to organized compilation and preservation.
- We are pledged to the compliance of all requirements as prescribed by national and international regulations.
- We firmly believe that our key to success is our QMS (Quality Management System) based on the cGMP requirements that ensure
effective controls applied to our work processes.
Our Quality Assurance is based on the following principles:
- All quality systems comply with all regulatory standards
- All the quality systems are in place and SOPs as :
- All equipment and utilities are qualified and Process & Cleaning validation activities are performed as per Validation Master Plan.
- All raw material and packaging material are purchased from approved vendors.
- All Finish products are released by QA Head post QC Reports
Quality Control Department:
Quality Control is an independent unit and responsible to carry out the analysis of :
- Raw materials,
- Packaging materials,
- In-process samples and
- Finished Products.
- Microbiological parameters.
We follow regularly updated methods for evaluation of the safety, efficacy, identity, strength and purity of our products, while facilitating innovation and improvement thereby adding value to our customers.
Showing 1–16 of 1702 results
