Pharmaceuticals
OUR DIVISION
End-to-End Pharmaceutical Excellence
At Baroque Pharmaceuticals, we offer complete end-to-end capabilities spanning formulation development, commercial manufacturing, and regulatory support—all under one unified ecosystem. Our operational approach is built upon three foundational commitments:
To your specific therapeutic & regulatory needs
Swift response to dynamic supply chain demands
At every step as your dedicated backend partner
Driven by experienced scientists and specialized support cells, we deliver complete R&D solutions—from sourcing, patent research, and formulation development to technology transfer, bioequivalence studies, and dossier lifecycle management. Our expertise spans diverse oral dosage forms, including immediate/extended-release tablets, capsules, liquid orals, and powders for suspension.
Our state-of-the-art EU GMP approved manufacturing plants ensure high-quality production and seamless regulatory compliance. Featuring dedicated facilities for Penicillins, Cephalosporins, and Non-Betalactams, we deliver a diverse range of dosage forms—including Tablets, Capsules, Oral Liquids, and Powder for Oral Suspension (PFOS). In addition to EU GMP approval, our manufacturing sites are inspected and approved by several regulatory authorities across Africa, Latin America and South-East Asia.
We offer our globally compliant dossiers for out-licensing and are also open for CMO and CDMO opportunities.
With an established operational structure across Europe, we offer comprehensive end-to-end support for seamless European market entry:
Leverage ready dossiers to file via Mutual Recognition Procedure (MRP) or Decentralized Procedure (DCP).
Fully EU-compliant release capabilities ensuring smooth market distribution.
Dedicated QP services for stringent regulatory compliance and product authorization.