Our Services
Raw Material & Excipient Testing
Implementing a raw material qualification programme with the assistance of a consultative Contract Research Organization (CRO) and contract development and manufacturing organization (CDMO) will enable drug developers to efficiently control the quality of raw materials and excipients used during drug development and manufacturing. Regulatory authorities such as the US Food and Drug Administration (FDA), International Council on Harmonization (ICH), and the International Organization for Standardization (ISO), Drug Regulatory Authority of Pakistan (DRAP) have released guidance documents outlining the regulatory requirements for testing pharmaceutical raw materials.
Pharmaceutical and raw material testing
Our raw material and finished product testing services provide manufacturers with peace of mind by ensuring the safety, purity, and quality of both starting material and manufactured products.
Method development and research services
Outsourcing your drug development and manufacturing activities creatively can assist your company in bringing new products to market in a timely and cost-effective manner. An effective collaboration with a strong CRO can continue to produce significant improvements.
Pharmaceutical container and packaging testing
We provide services for containers, container closure and pharmaceutical packaging including extractable and leachable studies.
General Questions
Raw materials are input substances used in both chemical synthesis and processing and include buffers, cleaning agents, common solvents and commonly used synthetic starting materials such as amino acids. Excipients are substances which are used as ingredients in pharmaceutical formulations such as tablets and capsules.
We provide services for contamination testing in syrups, suspensions, injectables and biologics.