Your Trusted Partner in Pharma Production
From formulation to packaging, our pharmaceutical contract manufacturing services deliver quality, scalability, and compliance. Let us bring your product to life with world-class facilities and end-to-end manufacturing support.
Pharmaceutical Contract Manufacturing
Humanaquest provides turnkey contract manufacturing solutions for APIs, solid and liquid formulations, sterile injectables, and more. Our end‑to‑end services span process development, scale‑up, cGMP production, and packaging—ensuring your products meet global quality and regulatory standards.
Whether you need small‑batch clinical supplies or large‑scale commercial runs, our integrated facilities and experienced team deliver on time, within budget, and fully compliant with CDSCO, FDA, and EMA guidelines.
Our Capabilities
- Process R&D and technology transfer
- Formulation development: tablets, capsules, liquids, creams
- Analytical method development & validation
- Pilot‑scale and commercial API synthesis
- Sterile manufacturing and lyophilization
- Regulatory dossier support (CTD, ANDA, DMF)
Our Facilities
Our multi‑site network includes cGMP‑certified plants for chemical synthesis, a fully‑equipped pilot plant, and dedicated formulation and packaging lines. All sites feature:
- Cleanrooms (ISO 7 & ISO 8)
- High‑throughput analytical laboratories
- 24/7 security and controlled access
- Automated blister and bottle filling
- Environmental monitoring & quality assurance
Why Choose Humanaquest?
- 20+ years of manufacturing excellence
- Dedicated project management & technical support
- Robust supply chain and risk mitigation
- Fully compliant with global regulatory authorities
- Flexible MOQs & rapid turnaround
- Transparent communication & on‑time delivery