R&D
Research & Development
At Chanelle Pharma, our in-house research and development capabilities are the cornerstone of our success and continued growth. As a generic medicines provider, our commitment to innovation is comparable to brand leaders in the industry.
Chanelle’s R&D laboratories in Ireland and Jordan include more than 70 scientists who innovate every day to develop and licence products in the Human and Animal Health market.
Our focus and commitment to R&D has allowed us to register over 5000 licenses in countries all over the world. Our R&D laboratories are equipped with the latest in R&D technology and highly competent and qualified staff who continuously engage in research studies and experiments to develop safe and effective medicines.
Our R&D Capabilities include:
Product Synthesis
Formulation Development
Process Validation
Stability Studies
Bio Equivalence Studies
Development & Validation
Registration Dossiers
Product Packaging
Consultancy Service
Regulatory Affairs
At Chanelle, we have an excellent registration team who have had consistent success in registering products all over the world.
Chanelle Pharma is a HPRA ( Health Products Regulatory Authority) licensed company for the manufacture of medicines licenses.
Our Regulatory Affairs department offers our customers worldwide regulatory assistance with the generation of detailed pharmacological, toxicological, safety and efficacy data for their product.
Chanelle Pharma laboratories in Jordan was established in 2008 and is a GMP Compliant Contract laboratory providing Physical, Chemical, Analytical & Formulation Solutions.
Chanelle Pharma Labs is subsidiary of Chanelle Pharma. Chanelle Pharma Labs consist of scientists and highly trained analysts, whose training is constantly enhanced through internal and external training.
