Finished dosage formulations developed and supplied to your specification — from oral solids to sterile injectables, backed by stability data and complete regulatory documentation.
Tablets and capsules developed and manufactured to IP / BP / USP standards.
Liquid orals and topical preparations with validated processes and packaging.
Sterile dosage forms manufactured at GMP-certified, approved facilities.
Registration-ready product dossiers to fast-track your market entry.
Documentation prepared to the format your target market requires.
Flexible commercial models to suit your business strategy.
We capture your dosage form, strength, pharmacopoeial standard (IP/BP/USP/EP) and target market requirements.
Lab-scale development and exhibit batches, with samples supplied for your evaluation and approval.
Stability studies, COA, dossier support (CTD/ACTD) and regulatory documentation for your submissions.
Third-party / contract manufacturing at GMP-certified sites with batch traceability and on-time delivery.
Production at WHO-GMP / GMP-certified facilities only.
Formulations compliant with IP, BP, USP or EP as required.
COA, BMR extracts and batch traceability with every supply.
CTD / ACTD documentation and stability data for registrations.
Share your requirement and our team will respond with technical details, documentation and pricing — fast.