Quality Assurance
At Mana Pharma, quality is built into every stage of process development, manufacturing, and operational execution. Our operations align with cGMP compliance and ICH guidelines, ensuring that our chemistry and manufacturing practices meet rigorous regulatory standards.
Our integrated R&D, process development, and analytical capabilities enable us to develop and optimize processes with a strong focus on reproducibility, scalability, and regulatory expectations. Whether managing our trusted CMO partnerships or scaling our upcoming manufacturing facility, we anchor every workflow in comprehensive technical documentation and data-driven decision-making.
We are committed to delivering consistent quality, reliable processes and scientifically sound solutions for our customers and partners.
Certificates & Quality Documents
Customers may request certificates, quality documents and product-specific information through our controlled enquiry process, in line with the product, customer requirement and confidentiality arrangements.
Certificate of Analysis
Per Batch
Safety Data Sheet
Per Product
Product Specification
On Request
Regulatory Support
We support pharmaceutical partners with technical and documentation discussions associated with APIs, intermediates, sourcing and manufacturing programmes. Regulatory information is shared according to the applicable product, development stage and document availability.
Customer & Supplier Qualification
Pharmaceutical partnerships depend on confidence in product quality, supply continuity and manufacturing practices. Our approach supports structured technical discussions and due-diligence requirements while respecting confidentiality and document-control needs.
Frequently Asked Questions
How can I request certificates or quality documents?
Through Mana Pharma's enquiry process, subject to product-specific availability and confidentiality requirements.
Can regulatory documentation be shared before a formal agreement?
Certain technical information can be discussed early; detailed documentation is generally shared once confidentiality arrangements are in place.
Do you support customer or supplier audits?
Yes. We support audit readiness and due-diligence discussions, subject to confidentiality and document-control requirements.
Need product-specific documentation?
Product-specific documentation and quality information can be made available upon request through a controlled enquiry process.