Quality Assurance
Ensure Your Medicines Meet the Highest International Standards
We deliver robust Quality Assurance services that uphold the integrity and consistency of your pharmaceutical products. From rigorous process validation and compliance with cGMP standards to comprehensive documentation review and batch certification, our QA support ensures full regulatory compliance and export readiness.
Compliance & Validation
- Implementation of cGMP across all production stages
- Process validation and risk assessment for critical operations
- Review and approval of master documents and specifications
Quality Documentation & QMS
- Development and maintenance of Quality Management Systems (QMS)
- Preparation and review of SOPs, manuals and batch records
- Change control support to manage updates in materials, methods or equipment
Batch Release & Audit Support
- Detailed review of batch manufacturing and testing data before release
- Deviation handling and CAPA (Corrective and Preventive Action) implementation
- Internal audits to ensure inspection readiness and continuous compliance
Training & Continuous Improvement
- Regular training programs to reinforce quality culture among staff
- Capability building to drive continuous process improvement
- Support in building a sustainable, long-term quality framework
Let’s Work Together
If you’re a healthcare provider, government buyer, or distributor looking to access trusted cancer medicines, we’re here to support you. Partner with Medivaara and help save lives — one shipment at a time.
Call Us 24/7
+91 9849181444
Mail Us Anytime
info@medivaara.com