Research & Development
Innovation Powered by Research
Chemical Product Modifications
1. Customization to increase the mineral content as per industry needs
2. Increase solubility according to dosage form
3. pH modification in products
Physical Product Modifications
1. Customize directly compressible grades and micronized powders
2. Optimize BD to produce effective application
Increased Purity
1. Low Heavy Metal Grades
2. Low Endotoxin Grades
3. High Purity Ingredients
Formulation Development Lab Service
1. Suitability of mineral salts in nal formulations
2. Comparative analysis of Product performance
3. Excipient performance
4. Pilot batch trials of fnished formulations
5. Prototype formulations for diverse nutritional supplements
Regulatory Support
Delivering the best regulatory compliant products
Beyond manufacturing, we stand by our clients and simply their compliance measures. Having had long experience of delivering a solution that meets various regulatory requirements, including 17 Products having USDMF registration, we are adept to deliver the following regulatory support:
1. Stability Data as per ICH
2. Residual Solvent as per ICH
3. Technical Data Package in CTD format for all products
4. Declarations available as per Global Regulations
5. Specs, MOA and MSDS as per current Global Standards
6. Preset VAQ for all customers as per Global Standards for better customer service
7. Documentations as per the ICH/IPEC guidelines
8. Drug Master File
Environment & Health Safety
At Vasa Pharmachem, we are committed to safeguarding the environment. We adhere to a scientifically defined EHS management system that ensures a safe and healthy work atmosphere & environment. At work, we practice the green philosophy for progress. And we have adopted a zero discharge philosophy for minimal impact on the already sensitive natural fabric. We also ensure minimal and smart usage of natural resources. As a governance policy, we encourage our employees to conserve paper, water, energy, and fuel at work and home. And we also participate in every initiative to conserve and enrich nature.
Customization
We understand that each client has unique requirements. Our R&D professionals work closely with clients to tailor our offerings, ensuring they align seamlessly with the end formulations.
1. Micronization
4. Directly Compressible Grades
7. Coated
2. Granulation
5. Co-processed Mineral
8. Pellets
3. Ultra-pure Grade
6. Premixes
9. Micro-Encapsulation
Quality Assurance
Vasa Pharmachem believes in being constant with providing the best quality. And that’s why we have complete Quality Management and Production Management systems through the Quality Control department that strictly follow cGMP standards and In-house quality standards.
Test and Retest are carried out on the facility equipment and production methods. The QMS of Vasa Pharmachem ensures high-quality standards.
Internal checks are conducted regularly to ensure constant improvement. And this is ensuring the quality and safety of the product.
With due consideration of the status of science and technology as well as the current requirements on the field of pharmacopeia and GMP Directives, the inspections take place in conformance with the certification documentation. Inspections are carried out on qualified devices using validated methods. Raw data of the system is recorded without gaps. And it ensures that the raw data, test reports, and other related material are archived.
Quality Control
We stand for quality, We are quality and Quality in everything we do.
Quality has been one of the vital aspects that have helped us distinguish ourselves. With scientifically defined management systems, we ensure that the only best quality of products leaves our manufacturing facilities.
Our quality initiatives are managed by a team of expert professionals. They are backed by technology and robust management systems. The various global accreditations only reinforce our commitment to quality. To foster trust further, we encourage facility audits for all of our prospective customers.
Quality Initiatives at a glimpse
1. Complete Quality Management and Production Management system-driven approach
2. Quality Control department with strict adherence to GLP standards Rigorous in-house quality standards and checks right from raw
3. Materials receipt to various stages of development and strict final product tests
4. Continuous QA inspection in compliance with the corresponding certification